Anup Kumar Misra
Professor
Anup Kumar Misra
Professor, Chemical Sciences
PhD: Indian Association for the Cultivation of Science (IACS) and Jadavpur University, Kolkata, India, 1997
Previous appointments:
Professor, Department of Chemical Sciences, Bose Institute, Kolkata, India January 2016-Till date
Associate Professor, Division of Molecular Medicine, Bose Institute, Kolkata, India August 2010-December 2015
Assistant Professor, Division of Molecular Medicine, Bose Institute, Kolkata, India October 2008-July 2010
Scientist-C and E1, Medicinal and Process Chemistry Division, Central Drug Research Institute (C.S.I.R), Lucknow, India Sept. 2001-Sept. 2008
Senior Research Scientist, Chembiotek Research Pvt. Ltd. (TCG Lifesciences), Kolkata 2000-2001
Postdoctoral Research Fellow with Prof. Ole Hindsgaul and Prof. Minoru Fukuda, The Burnham Institute, La Jolla, USA 1998-2000
Postdoctoral Research Fellow with Prof. R. A. Field and Prof. S. W. Homans, University of St. Andrews, Scotland 1997-1998
Research interests:
Main research interest is to develop synthetic strategies for the synthesis of complex saccharide molecules of biological interest and their glycoconjugates to use them in the immunochemical studies towards the preparation of anti-microbial vaccine candidates.
The group is also engaged in the design and synthesis of medicinally important small molecules (e.g. anti-filarial, anticancer agents, antioxidantsis and enzyme inhibitors etc ) and their bioevaluation in a collaborative program
Contact:
Address: |
Chemical Sciences Unified Academic Campus Bose Institute EN-80, Sector V Bidhan Nagar Kolkata - 700 091, India |
E-Mail: | anup[at]jcbose.ac.in |
Phone: | +91-33-25693266 |
Research:
1. Design and Syntheses of molecules for
their biological evaluation
(a) In continuation of our ongoing program on the synthesis and bioevaluation of natural products and their analogs a series of glycosyl trizolyl terpenoid derivatives were synthesized and evaluated for their anticancer activities against different cancer cells. Several compounds were found anticancer agents and their detailed biological studies are under progress.
(b) A series of analogs of Resveratrol, a well known
anticancer agent were prepared and their evaluation as anti filarial agents and
anticancer agents are under progress.
(c) A series of aryl bisindolylmethane derivatives
were prepared using an eco-friendly condition in water and their evaluation as
CA-ATPase modulator and anticancer agent is ongoing.
(d) Cell wall glycoconjugates corresponding to the
Meningitidis type X and A (MenX and A) have been prepared by the synthesis of
the respective cell wall polysaccharide fragments by chemical glycosylations
and then coupled with tetanus toxoid protein. The glycol-protein conjugates
were evaluated for their antigenic functions and found promising lead for the
development of the meningococcal vaccines.
(e) A
collaborative program has been initiated under DST twinning project for the
isolation, characterization and bioevaluation of natural products and
preparation of their synthetic analogs.
2. Studies on synthetic organic chemistry particularly carbohydrate chemistry:
A large number of complex oligosaccharides corresponding to the antigenic cell wall polysaccharides of pathogenic bacteria have been synthesized using several novel techniques. These synthetic oligosaccharides act as important precursors for the preparation of glycoconjugates by attaching them with appropriate proteins under reductive amination methodologies. Synthetic glycoconjugates will be used to raise antibodies against them for their application in the development of diagnostic markers as well as antimicrobial agents.
A number of
synthesized oligosaccharides were subjected to Molecular dynamics simulation
studies to get the conformational structural insights of the compounds for
designing glycomimetics corresponding to these molecules.
Publications:
161. Si A & Misra AK. Facile synthesis of a rare
sugar intermediate: D-gulopyranosyl cyanide. Trends Carbohydr. Res., 9,
63 - 66 (2017).
160. Bhaumik I & Misra AK. Convergent synthesis of the tetrasaccharide repeating unit of the O-polysaccharide
of Salmonella enterica O41. Chemistry Select, 2, 3065 - 3067
(2017).
159. Ghosh T, Si A & Misra AK. Facile transformation of nitriles into thioamides: Application
to C-Glycosyl Nitrile Derivatives. Chemistry Select, 2, 1366 -
1369 (2017).
158. Bhaumik I & Misra
AK. Concise synthesis of a pentasaccharide repeating unit corresponding to
the O-Antigen of Salmonella enterica O51. Chemistry
Select, 2, 937 - 939 (2017).
157. Roy C, Alam M, Mandal S, Haldar PK, Bhattacharya S, Mukherjee T, Roy R,
Rameez MJ, Misra AK, Chakraborty R, Nanda AK, Mukhopadhyay SK & Ghosh W. Global association between thermophilicity and vancomycin susceptibility
in bacteria. Front. Microbiol, 7:412 (2016). doi:
10.3389/fmicb.2016.00412.
156. Chakraborty
S, Ghosh S, Banerjee B, Santra A, Adhikary A, Misra AK & Sen PC. Phemindole, a synthetic di-indole derivative maneuvers the store operated
calcium entry (SOCE) to induce potent anti-carcinogenic activity in human
triple negative breast cancer cells. Frontiers in Pharmacology, 7, 114/1 - 114/21 (2016).
155. Chakraborty
S, Ghosh S, Banerjee B, Santra A, Bhat J, Adhikary A, Chatterjee S, Misra AK
& Sen PC. Mephebrindole, a synthetic indole analog coordinates
the crosstalk between p38MAPK and eIF2α/ATF4/CHOP signalling pathways for
induction of apoptosis in human breast carcinoma cells. Apoptosis, 21, 1106 - 1124 (2016).
154. Bhaumik I & Misra AK. Expedient synthesis of the
pentasaccharide repeatingunit of the O-antigen of Escherichia coli O86and its conformational analysis. Glycoconj J,
33, 887 - 896 (2016).
153. Si A
& Misra AK. Synthesis of a pentasaccharide
repeating unit corresponding to the cell wall O-antigen of Escherichia coli O59
using iterative glycosylations in one pot. Tetrahedron, 72, 4435 -
4444 (2016).
152. Gucchait A,
Jana M, Jana K & Misra AK. Preparation of glycosyl
thiourea derivatives from glycosyl azides using sulfamic acid and sodium iodide
in one-pot. Carbohydrate Research, 434, 107 - 112
(2016).
151. Roy P, Dhara D, Parida PK, Kar
RK, Bhunia A, Jana K, Sinha Babu SP & Misra AK. C-Cinnamoyl glycosides
as a new class of anti-filarial agents. Eur. J. Med. Chem, 114, 308 - 317 (2016).
150. Mukherjee N, Parida PK, Santra A, Ghosh T, Dutta A, Jana K,
Misra AK & Sinha Babu SP. Oxidative stress plays major role in mediating
apoptosis in filarial nematode Setaria cervi in the presence of trans-stilbene
derivatives. Free
Rad. Biol. Med., 93,
130 - 144 (2016).
149. Rahkila
J, Misra AK, Guazzelli L & Leino R. Glycosylation of phenolic acceptors
using benzoylated glycosyl trichloroacetimidate donors. Carbohydrate Chemistry:
Proven Synthetic Methods, 3, 97 - 105 (2015).
148. Misra AK, Bokor É, Kun S, Bolyog-Nagy E, Kathó Á, Joó F, Somsák L. Chemoselective hydration of glycosyl cyanides to C-glycosyl formamides
using ruthenium complexes in aqueous media. Tetrahedron Letters, 56, 5995 - 5998 (2015).
147. Si A
& Misra AK. Expedient synthesis of the pentasaccharide repeating unit
of the polysaccharide O-antigen of Escherichia coli O11. Chemistry Open, 5, 47 - 50 (2015).
146. Ghosh
T & Misra AK. Facile synthesis of the heptasaccharide repeating unit of the
cell wall O-polysaccharide of
enterotoxigenic Escherichia coli
O139. Chemistry Open, 5, 43 - 46 (2015).
145. Santra
A, Ghosh T
& Misra AK. Synthesis of di- and
trisaccharides related to the O-polysaccharide of Shigella dysenteriae
type 8. J. Carbohydr. Chem., 34, 501 - 513 (2015).
144. Dhara
D & Misra AK. Convergent Synthesis of Oligosaccharide
Fragments Corresponding to the Cell Wall O-Polysaccharide of Salmonella
enterica O53. Chemistry Open, 4, 768 - 773 (2015).
143. Jana M
& Misra AK. Synthesis of trisaccharide and a tetrasaccharide repeating unit
corresponding to the O-antigen of
Shiga toxin producing Escherichia coli O177. Tetrahedron, 71, 3960 - 3965 (2015).
142. Harale KR, Dumare NB, Singh D, Misra AK & Chhikara MK. Synthesis of a tetrasaccharide and its glycoconjugate corresponding to
the capsular polysaccharide of Neisseria meningitidis serogroup
X and its immunochemical studies. RSC: Adv., 5, 41332 - 41340 (2015).
141. Si A
& Misra AK. Efficient synthesis of the pentasaccharide repeating unit
of the O-antigenic polysaccharide of Escherichia coli O166 strain. Synthesis, 47, 83 - 88 (2015).
140. Bhaumik I & Misra AK. Expedient synthesis of a pentasaccharide related to the
O-specific polysaccharide of Escherichia coli O117:K98:H4 strain. RSC: Adv., 4, 61589 - 61595 (2014).
139. Ghosh
T, Kar RK, Bhunia & Misra AK. Synthesis of the pentasaccharide repeating unit of the O-antigen of
Escherichia coli O175 using one-pot glycosylations and its conformational
analysis. Tetrahedron,
70, 9262 - 9267 (2014).
138. Bhaumik I,
Ghosh T & Misra AK. Efficient synthesis of the tetrasaccharide repeating
unit of the O-antigen of Escherichia coli O174 strain. Carbohydr. Res., 399, 21 - 25 (2014).
137. Jana M,
Kar RK, Bhunia & Misra AK. Synthesis of the tetrasaccharide
repeating unit of the O-antigen of Escherichia coli O69 strain and its
conformational analysis. RSC Adv., 4,
37079 - 37084 (2014).
136. Mandal PK, Dhara D & Misra AK. Concise synthesis of the
repeating units of the cell wall lipopolysaccharide of Azospirillum
brasilense SR80. Synthesis, 1947 - 1953 (2014).
135. Parida PK, Sau A, Ghosh
T, Jana K, Biswas K, Raha S &
Misra AK. Synthesis and evaluation of triazole linked glycosylated 18b-glycyrrhetinic
acid derivatives as anticancer agents. Bioorganic Medicinal Chem. Letters, 24, 3865 - 68
(2014).
134. Dhara
D, Kar RK, Bhunia & Misra AK. Convergent synthesis and
conformational analysis of the hexasaccharide repeating unit of the O-antigen of Shigella flexneri serotype 1d. European Journal of Organic Chemistry, 4577 - 4584
(2014).
133. Santra
A, Si A, Kar RK, Bhunia A & Misra AK. Linear synthesis and
conformational analysis of the pentasaccharide repeating unit of the cell wall O-antigen of Escherichia coli O13. Carbohydrate Research, 391, 9 - 15 (2014).
132. Jana
M, Sau A & Misra AK. Synthesis
of a pentasaccharide repeating unit of the O-antigen
of enteroadherent Escherichia coli
O154 strain. Tetrahedron:
Asymm., 25,
632 - 636 (2014).
131. Dhara
D, Mandal PK & Misra AK. Convergent synthesis of a
pentasaccharide repeating unit corresponding to the cell wall O-antigen of
Salmonella enteric O44. Tetrahedron: Asymmetry, 25, 263 - 267 (2014).
130. Mandal
PK, Dhara D & Misra AK. Convergent synthesis of a
tetrasaccharide repeating unit of the O-specific polysaccharide from the cell
wall lipopolysaccharide of Azospirillum brasilense strain Sp7. Beilstein J. Org. Chem.,
10, 293 - 299 (2014).
129. Ghosh
T, Santra A &
Misra AK. Convergent
synthesis of a hexasaccharide corresponding to the cell wall O-antigen of Escherichia coli O41. RSC Adv., 4, 54 - 60 (2014).
128. Sau A, Dhara D & Misra AK. Concise
synthesis of a pentasaccharide repeating unit corresponding to the O-antigen of Escherichia coli O102. Tetrahedron: Asymmetry, 24, 942 - 946 (2013).
127. Jana
M & Misra AK. Concise synthesis of the
tetrasaccharide repeating unit of the O-antigen of Escherichia coli O16. Beilstein J. Org. Chem., 9, 1757 - 1762 (2013).
126. Dhara
D & Misra AK. Expedient
synthesis of a tetrasaccharide and a pentasaccharide corresponding to the cell
wall O-antigen of Escherichia coli O77 and Escherichia coli O17. Tetrahedron: Asymmetry, 24, 1488 - 1494 (2013).
125. Santra
A & Misra AK. Synthesis of a common
tetrasaccharide repeating of the O-antigen of enteroinvasive Escherichia coli O143 and Shigella boydii type 8. Current Organic
Synthesis, 10,
178 - 182 (2013).
124. Ghosh T, Santra A & Misra AK. Facile synthesis of a
pentasaccharide repeating unit corresponding to the common O-antigen of Salmonella
enterica O57 and E. coli O51. Tetrahedron: Asymmetry,
24, 606 - 611 (2013).
123. Guchhait G & Misra AK. Short synthesis of the common trisaccharide core of
kankanose and kankanoside isolated from Cistanche
tubulosa. Beilstein J. Org. Chem., 9, 705 - 709 (2013).
122. Jana M & Misra AK. Stereoselective synthesis of b-glycosyl thiols and their synthetic applications. J. Org. Chem., 78, 2680 - 86 (2013).
121. Santra
A, Guchhait G & Misra AK. Nitrosyl tetrafluoroborate
catalyzed preparation of 2,3-unsaturated and 2-deoxy glycosides of hindered
alcohols, thiols and sulfonamides. Synlett, 24 581 - 586 (2013).
120. Ghosh T, Santra A & Misra AK. Appel reagent mediated transformation of glycosyl
hemiacetal derivatives into thioglycosides and glycosyl thiols. Beilstein J.
Org. Chem., 9,
974 - 982 (2013).
119. Santra
A, Ghosh T & Misra AK. Removal of benzylidene acetal and
benzyl ether in carbohydrate derivatives using triethylsilane and Pd/C.
Beilstein J. Org. Chem., 9, 74 - 78 (2013).
118. Sau A & Misra AK. Convergent synthesis of the tetrasaccharide repeating unit
of the cell wall lipopolysaccharide of Escherichia
coli O40. Beilstein J. Org. Chem., 8, 2053 - 2059 (2012).
117. Jana
M & Misra AK. Significantly
fast synthesis
of glycosyl dithiocarbamate and trithiocarbonate derivatives under solvent-free
condition. Synlett, 23,
2789 - 2794 (2012).
116. Sau A, Santra
A & Misra AK. Stereoselective glycosylations by nitrosyl tetrafluoroborate catalyzed
activation of glycosyl trichloroacetimidate derivatives. Synlett, 23, 2341 - 2348 (2012).
115. Ghosh
T & Misra AK. Facile synthesis of the
pentasaccharide repeating unit of the cell wall O-antigen of Escherichia coli
19ab. Carbohydrate Research, 362, 8 - 12 (2012).
114. Santra
A, Ghosh T & Misra AK. Expedient synthesis of two
structurally close tetrasaccharides corresponding to the O-antigens of Escherichia
coli O127 and S. enterica O13. Tetrahedron: Asymmetry, 23, 1385 - 1392 (2012).
113. Sau A & Misra AK. Reaction of glycal derivatives with
alcohols in the presence of N-Bromosuccinimide
(NBS) and diphenyldiselenide: Preparation of 2-deoxy-2-phenylselenyl
glycosides. Carbohydrate Research, 361, 41 - 48 (2012).
112. Sau A & Misra AK. Synthesis of the tetrasaccharide
motif and its structural analog corresponding to the O-specific lipopolysaccharide of Escherichia coli O75. PLoS: One, 7, e37291 (2012).
111. Santra A & Misra AK. Convergent synthesis of the pentasaccharide repeating unit
of the O-antigenic polysaccharide of enterohaemorrhagic Escherichia coli O113. Glycoconjugate Journal, 29, 181 - 188 (2012).
110. Sau A, Panchadhayee R, Ghosh D & Misra AK. Synthesis of a tetrasaccharide
analog corresponding to the repeating unit of the O-polysaccharide of Salmonella
enterica O59: Unexpected stereo outcome in glycosylation. Carbohydrate
Research, 352,
18 - 22 (2012).
109. Guchhait G & Misra AK. Convergent synthesis of the tetrasaccharide repeating unit
corresponding to the O-antigen of the vero-toxin producing E. coli O176.
Glycoconjugate Journal, 28, 519 - 524 (2011).
108. Santra A & Misra AK. Convergent synthesis of the tetrasaccharide repeating
unit of the O-antigen of Shigella boydii type 9. Beilstein
J. Org. Chem., 7, 1182 - 1188 (2011).
107. Panchadhayee R & Misra AK. Convergent synthesis of
the pentasaccharide repeating unit of the O-antigen
of Shigella boydii type 14. Tetrahedron:
Asymmetry, 22, 1390 - 1394 (2011).
106. Guchhait G & Misra AK. Efficient glycosylation of
unprotected sugars using sulfamic acid: a mild eco-friendly catalyst. Catalysis
Communications, 14,
52 - 57 (2011).
105. Guchhait G & Misra AK. Environmentally benign synthesis of 2,3-unsaturated glycopyranosides
in task-specific ionic liquid. Catalysis Letters, 141, 925 - 930 (2011).
104. Sau A & Misra AK. Odorless eco-friendly synthesis of
thio- and selenoglycosides in ionic liquid. Synlett, 1905 – 1911 (2011).
103. Santra A & Misra AK. Synthesis of thioglycosides in room
temperature ionic liquid. J. Carbohydr. Chem., 30, 85 - 93 (2011).
102. Sau A & Misra AK. Environmentally benign preparation
of benzylidene acetal of carbohydrate derivatives in PEG 600. J. Carbohydr.
Chem., 30,
41 - 46 (2011).
101. Santra A, Guchhait G & Misra AK. Efficient acylation and sulfation
of carbohydrates using sulfamic acid, a mild, eco-friendly catalyst under
organic solvent-free condition. Green Chemistry, 13, 1345 - 51 (2011).
100. Guchhait G & Misra AK. Convergent synthesis of a common
pentasaccharide corresponding to the O-antigen of Escherichia coli O168 and
Shigella dysenteriae type 4. Glycoconjugate Journal, 28, 11 - 19 (2011).
99. Santra
A & Misra AK. Synthesis of tri- and penta-saccharide fragments
corre-sponding to the O-abtigen of Shigella boydii type 6. Tetrahedron:
Asymmetry, 21,
2612 - 2618 (2010).
98. Ghosh
S & Misra AK. Synthesis of the hexasacch-aride repeating unit
corres-ponding to the cell wall lipopoly-saccharide of Azospirillum irakense
KBC1. Tetrahedron: Asymmetry, 21, 2755 - 2761 (2010).
97. Mukherjee C, Ghosh S, Nandi P, Sen PC & Misra AK. Efficient synthesis of
(6-deoxy-glycopyranosid-6-yl)-sulfone derivatives and their effect on Ca2+-ATPase.
Eur. J.
Med. Chem., 45,
6012 - 6019 (2010).
96. Panchadhayee R & Misra AK. Convenient synthesis of penta- and
hexasaccharide fragments corresponding to the O-antigen of Escherichia coli
O150. Tetrahedron: Asymmetry, 21, 2142 - 2152 (2010).
95. Panchadhayee R & Misra AK. Convergent
synthesis of a common pentasaccharide repeating unit corresponding to the
O-specific polysaccharide of Escheriachia coli O4: K3, O4:K6 and O4:K12. Tetrahedron:
Asymmetry, 21, 859 - 863 (2010).
94. Ghosh
S & Misra AK. Synthesis of a hexasaccharide corresponding to Azospirillum
lipoferum Sp59b lipopolysaccharide. Tetrahedron: Asymmetry, 21, 725 - 730 (2010).
93. Panchadhayee R & Misra AK. Regioselective
reductive ring-opening of benzylidene acetals using triethylsilane and I2.
Synlett,
1193 - 1196 (2010).
92. Singh
S, Mandal PK, Singh N, Misra AK, Singh S, Chaturvedi V, Sinha S & Saxena
AK. Substituted hydrazinecarbothioamide as potent antitubercular agents:
Synthesis and quantitative structure–activity relationship (QSAR). Bioorg. Med.
Chem. Lett., 20, 2597 - 2600 (2010).
91. Panchadhayee R & Misra AK. Removal of anomeric allyl group
using N-bromo succinimide (NBS): preparation of glycosyl hemiacetals. J.
Carbohydr. Chem., 29,
76 - 83 (2010).
90. Mandal
PK & Misra AK. Concise Synthesis of the
pentasaccharide O-antigen corresponding to the Shiga toxin producing
Escherichia Coli O171. Bioorganic Chemistry, 38, 56 - 61 (2010).
89. Guchhait G
& Misra AK. Synthesis of the trisaccharide O-antigen of Rahnella
aquatilis 1-95. J. Carbohydr. Chem., 29, 1 - 9 (2010).
88. Ghosh
S & Misra AK. Synthesis of a tetra-saccharide corresponding to the
teichoic acid from the cell wall of Strepto-myces sp. VKM Ac-2275. Tetrahedron:
Asymmetry, 20, 2688 - 93 (2009).
87. Panchadhayee R & Misra AK. Synthesis
of tri- and disaccharide fragments related to the O-antigen of enteropathogenic
Escherichia coli O158. J. Carbohydr. Chem., 29, 39 - 50 (2010).
86. Ghosh
S & Misra AK. Concise synthesis of a
hexasaccharide related to the adhesin receptor of Streptococcus oralis ATCC
55229. J.
Carbohydr. Chem., 28,
447 - 462 (2009).
85. Mukherjee
C & Misra AK. Synthesis of (6,6¢)-C-linked pseudodisaccharides. J. Carbohydr. Chem., 28, 475 - 482 (2009).
84. Guchhait
G & Misra AK. Total synthesis of the heptasaccharide of the iron-binding
exopoly-saccharide secreted by Klebsiela oxytoca BAS-10. Tetrahedron:
Asymmetry, 20, 1791 - 1797 (2009).
83. Pandey
S, Ghosh S & Misra
AK. Synthesis of a tri and tetra-saccharide present in the cell
wall lipopolysaccharides of Azospirilum brasilense S17. Synthesis,
2584 - 2590 (2009).
82. Mandal
PK & Misra AK. Efficient synthesis of two
sialylated tetrasaccharides found in goat milk. Synthesis, 1348 - 1354 (2009).
81. Panchadhayee
R & Misra AK. First synthesis of a
pentasaccharide repeating unit of the O-antigenic polysaccharide from
enterohemorrhagic E. coli O48:H21. Tetrahedron: Asymmetry, 20, 1550 - 1555 (2009).
80. Mukherjee C & Misra AK. Total synthesis of a unique
tetrasaccharide present in the Human Clotting Factor IX and mammalian Notch 1
receptor. Tetrahedron: Asymmetry, 20, 473 - 477 (2009).
79. Mandal
PK, Maiti GH & Misra AK. Facile synthesis of a
tetrasaccharide corresponding to the capsular polysaccharide of Streptococcus
pneumoniae type 15B. Arkivoc,
(ii), 281 - 287 (2009).
78. Panchadhayee R & Misra
AK. Odorless regioselctive ring opening of epoxides with S-alkylisothio-uronium
salts as masked thiols in water. Arkivoc, (ii) 298 - 307 (2009).
77. Ghosh S, Misra AK, Bhatia G, Khan M & Khanna A. Syntheses
and evaluation of glucosyl aryl thiosemi-carbazide and glucosyl
thiosemicarbazone derivatives as antioxidant, anti-dyslipidemic agents. Bioorg.
Med. Chem. Lett., 19, 386 - 389 (2009).
76. Mukherjee C & Misra
AK. Synthesis of a unique trisaccharide having an acetal linkage between
openchain and cyclic sugar found in the cell wall of Proteus. Tetrahedron: Asymm.,
19, 2746 - 51 (2008).
75. Panchadhayee R & Misra AK. Efficient preparation of
benzylidene acetal in carbohydrate derivatives. J. Carbohydr. Chem., 27, 148 - 155 (2008).
74. Mandal
PK & Misra AK. Concise synthesis of the pentasaccharide O-antigen of
Escherichia coli O83 present in colinfant vaccine. Glycoconjugate J., 25, 713 - 722 (2008).
73. Kumar
R, Maulik PR & Misra AK. Concise chemical synthesis of a tetrasaccharide
repeating unit of the O-antigen of Hafnia alvei 10457. Glycoconjugate
J., 25, 511 - 519 (2008).
72. Mukherjee
C & Misra AK. Total synthesis of an antigenic heptasaccharide motif found
in the cell-wall lipooligosaccharide of Mycobacterium gordonae strain 989. Glycoconjugate
J., 25, 611 - 624 (2008).
71. Tiwari
P & Misra AK. Synthesis of oligosaccharide fragments corresponding to the
exopolysaccharide released by Streptococcus macedonicus Sc 136. Glycoconjugate J., 25, 85 - 99 (2008).
70. Mukherjee C & Misra
AK. First
total synthesis of a pentasaccharide repeating unit of the O-antigen of Hafnia
alvei PCM 1529. Glycoconjugate J., 25, 111 - 119
(2008).
69. Kumar
R, Maulik PR & Misra AK. Significantly rapid access to glycosyl triazole and
tetrzoles from reducing sugars in one-pot. Glycoconjugate J., 25, 595 - 602
(2008).
68. Mandal
PK & Misra AK. Catalyst-free efficient synthesis of 3-thio-2-deoxysugar
derivatives in water. J. Carbohydr. Chem., 27, 238 - 257 (2008).
67. Panchadhayee R & Misra AK. Concise synthesis of a
heptasaccharide antigen found in the cell-wall lipopolysaccharide of M.
gordonae strain 990. Glycoconjugate J., 25, 817 - 826 (2008).
66. Mandal
PK & Misra AK. Efficient acetylation and preparation of Boc derivatives of
carbohydrate, amines and phenols. Letters in Organic Chemistry, 5, 194 - 201
(2008).
65. Ghosh
S, Tiwari P, Pandey S, Misra AK, Chaturvedi V, Gaikwad A, Bhatnagar S & Sinha
S. Synthesis and evaluation of antitubercular activity of glycosyl thio- and
sulfonyl acetamide derivatives. Bioorg. Med. Chem. Lett., 18, 4002 - 4005 (2008).
64. Mandal
PK & Misra AK. Concise synthesis of two
pentasaccharides corresponding to the a-chain oligosaccharides of N. gonorrhoeae and N.
meningitides. Tetrahedron, 64,
8685 - 8691 (2008).
63. Mukherjee C,
Maiti
GH & Misra AK. Regioselective ring opening of epoxides with thiols in water. Arkivoc, (xi) 46 - 55 (2008).
62. Mandal
PK & Misra AK. Synthesis
of Oligosaccharides Corresponding to the Polysaccharides of Lactobacillus and Thermophilus Strains. Synthesis, 2660 - 2666 (2007).
61. Agnihotri
G, Mandal PK & Misra AK. Concise synthesis of two
trisaccharide analogs related to the glycone constituent of Phanoside, a novel
insulin releasing natural product. Tetrahedron, 63, 7240 - 45 (2007).
60. Tiwari
P & Misra AK. Synthesis of a pentasaccharide repeating unit of the
extracellular polysaccharide produced by L. delbrueckii subsp. bulgaricus 291. J.
Carbohydr. Chem., 26,
239 - 248 (2007).
59. Kumar
R, Maulik PR & Misra AK. Synthesis of glycosyl enaminones from glycosyl
azides.
J. Carbohydr. Chem., 26, 83 - 90 (2007).
58. Mukherjee C & Misra
AK. Odorless
preparation of thioglycosides and thio michael adducts of carbohydrate
derivatives. J. Carbohydrate Chemistry, 26, 213 - 221 (2007).
57. Mukherjee C & Misra AK. Glycosylation and pyranose-furanose
isomerization of carbohydrates using HClO4-SiO2:
Synthesis of oligosaccharides containing galactofuranose. Synthesis, 683 - 692
(2007).
56. Mukherjee C & Misra
AK. Aza-Michael
addition of amines to activated alkenes catalyzed by Silica suppo-rted
perchloric acid under a solvent-free condition. Letters in Organic Chemistry,
4, 54 - 59 (2007).
55. Mandal
PK & Misra AK. Mild and efficient hydrolysis of thioglycosides to glycosyl
hemiacetals using N-iodosaccharin. Synlett, 1207 - 1210 (2007).
54. Madhusudana
KP, Kumar B, Kanojiya S, Agnihotri G & Misra AK. Tandem mass spectra of
divalent metal ion adducts of glycosyl sulfides, sulfoxides and sulfones,
distinction among stereoisomers. J. Mass Spectrometry, 41, 1322 – 1333 (2006).
53. Agnihotri
G
&
Misra AK. Synthesis
of a di- and a trisaccharide related to the O-antigen of Escherichia coli O83:
K24: H31. Carbohydrate Research, 341, 2420 - 2425 (2006).
52. Tiwari
P, Puri A, Chander, Bhatia G & Misra AK. Synthesis and antihyperlipidemic activity
of novel glycosyl fructose derivatives. Bioorg. Med. Chem. Lett., 16, 6028 - 6033 (2006).
51. Agnihotri
G & Misra AK. Facile synthesis of pyruvate ketals of carbohydrates. Tetrahedron
Letters, 47,
8493 - 97 (2006).
50. Agnihotri
G, Tiwari P & Misra AK. Unprecedented transforma-tion of thioglycosides to their
corresponding 1-O-acetates in the presence of HClO4-SiO2.
Journal of Carbohydrate Chemistry, 25, 491 - 498 (2006).
49. Mandal
PK & Misra AK. HClO4-SiO2 catalyzed multicomponent
reactions for the synthesis of privileged heterocyclic structures. Letters in
Organic Chemistry, 3,
848 - 853 (2006).
48. Tiwari
P & Misra AK. An Efficient Stereoselective Dihydroxylation of Glycals
using a Bimetallic System, RuCl3/CeCl3/NaIO4. Journal
of Organic Chemistry, 71, 2911 - 2913 (2006).
47. Kumar
R, Tiwari P, Maulik PR & Misra
AK. HClO4-SiO2
catalyzed chemoselective synthesis of acylals from aldehydes under solvent-free
conditions. Journal of Molecular Catalysis: A, 247, 27 - 30 (2006).
46. Tiwari
P & Misra AK. Acylation of carbohydrates over Al2O3:
preparation of partially and fully acylated carbohydrate derivatives and
acetylated glycosyl chlorides. Carbohydrate Research, 341, 339 - 350 (2006).
45. Mukherjee
C, Tiwari P & Misra AK. Synthesis of thio- and
selenoglycosides by cleavage of dichalconides in the presence of zinc/zinc
chloride and reaction with glycosyl bromides. Tetrahedron Letters, 47, 441 - 445 (2006).
44. Tiwari
P & Misra AK. Indium(I) iodide mediated efficient synthe-sis of
selenoglycosides. Tetrahedron Letters, 47, 2345 - 48 (2006).
43. Agnihotri G
& Misra AK. Fast oxidation of thioglycosides to glycosyl sulfones using KMnO4/CuSO4·5H2O
under neutral reaction conditions. Carbohydrate Research, 341, 275 - 280 (2006).
42. Tiwari P & Misra
AK. Selective
removal of anomeric O-acetate groups in carbohydrates using HClO4-SiO2.
Tetrahedron Letters, 47, 3573 - 76 (2006).
41. Agnihotri G
& Misra AK. Mild and efficient method for the cleavage of benzyli-dene acetals
using HClO4–SiO2 and direct conversion of acetals to
acetates. Tetrahedron Letters, 47, 3653 - 3658 (2006).
40. Kumar R, Tiwari P, Maulik PR & Misra AK. A Generalized Procedure
for the One-Pot Preparation of Glycosyl Azides and Thioglycosides Directly from
Unprotected Reducing Sugars under Phase Transfer Conditions. European Journal
of Organic Chemistry, 74 - 79 (2006).
39. Agnihotri G
& Misra AK. Fast and selective oxidation of
thioglycosides to glycosyl sulfoxides using KF/m-CPBA. Tetrahedron Letters, 46, 8113 - 16 (2005).
38. Tiwari
P, Kumar R & Misra AK. Efficient acetylation of carbohydrates promoted by
imidazole. Eur. J. Organic Chemistry, 4265 - 4270 (2005).
37. Tiwari
P, Agnihotri G & Misra AK. Modified one-pot protocol for the
preparation of thioglycosides from unprotectted aldoses via S-glycosyl
isothiouronium salts. Journal of Carbohydrate Chemistry, 24, 723 - 732 (2005).
36. Kumar
R, Tiwari P, Maulik PR & Misra
AK. Comparative structural analysis of 5,6,7,9-tetra-O-acetyl-4,8-anhydro-1,3-dideoxy-d-glycero-l-gluco-nonulose
and its 1-O-acetylated analog, 1,2,3,4,6-penta-O-acetyl-β-d-galactopyranose
using X-ray crystallography. Carbohydrate Research, 340, 2335 - 2339 (2005).
35. Madhusudan
SK & Misra AK. Synthesis of a new type of glycosidic linkage: Acetal linked
disaccharides and trisaccharides of acyclic and cyclic sugars.
Eur.
J. Organic Chemistry, 3196 - 3205 (2005).
34. Madhusudan
SK & Misra AK. Facile exchange of glycosylS,S-acetals to their O,O-acetals and
prepara-tion of glycofuranosides from acyclic glycosyl S,S-acetals under
metal-free reaction conditions in the presence of
1,3-dibromo-5,5-dimethylhydantoin. Carbohydrate Research, 340, 497 - 502 (2005).
33. Misra
AK, Tiwari P & Agnihotri G.
Ferrier
rearrangement catalyzed by HClO4-SiO2: Synthesis of
2,3-unsaturated glycopyranosides. Synthesis, 260 - 266 (2005).
32. Tiwari P, Agnihotri G &
Misra AK. Synthesis of
2,3-unsatura-ted C-glycosides by HClO4-SiO2 catalyzed
ferrier rearrangement of glycals. Carbohydrate
Research, 340, 749 - 752 (2005).
31. Misra
AK, Tiwari P & Madhusudan SK. HClO4-SiO2
catalyzed per-O-acetylation of carbohydrates. Carbohydrate Research, 340, 325 - 329 (2005).
30. Madhusudan
SK, Agnihotri G, Negi DS & Misra AK. Direct one-pot conversion of
acylated carbohydrates into their alkylated deriva-tives under heterogeneous
reaction conditions using solid NaOH and a phase transfer catalyst. Carbohydrate
Research, 340,
1373 - 1377 (2005).
29. Madhusudana
KP, Kumar B, Tiwari P, Madhusudan SK & Misra AK. Effect of metal
cationization on the tandem mass spectra of glycosyl dithioacetals. Journal of
Mass Spectrometry, 40,
25 - 35 (2005).
28. Agnihotri
G, Tiwari P & Misra AK. One-pot synthesis of per-O-acetylated thioglycosides from
unprotected reducing sugars. Carbohydrate Research, 340, 1393 - 1396 (2005).
27. Madhusudana KP, Tiwari
P,
Madhusudan SK & Misra AK. Tandem mass spectra of transition-metal ion adducts of
glycosyl dithioacetals; distinction among stereoisomers. Rapid Commun. Mass
Spectrometry, 19,
470 - 476 (2005).
26. Misra AK &
Agnihotri
G. Chloramine–T mediated chemoselective hydrolysis of
thioglycosides into glycosyl hemiacetals under neutral condition. Carbohydrate
Research, 339,
885 - 890 (2004).
25. Misra AK &
Agnihotri
G. Preparation of polyhydroxyalkyl-
and C-glycosylfuran derivatives from free sugars catalyzed by cerium(III)
chloride in aqueous solution: an improvement of the Garcia Gonzalez reaction. Carbohydrate Research, 339, 1381 - 1387 (2004).
24. Misra AK, Agnihotri
G, Madhusudan SK & Tiwari P. Practical synthesis of
sulfated analogs of lactosamine and sialylated lactosamine derivatives. J. Carbohydrate Chemistry,
23, 191 - 199 (2004).
23. Misra
AK, Agnihotri G & Madhusudan SK. Microwave induced eco-friendly solvent-free
Biginelli reaction catalyzed by calcium chloride. Ind. J. Chem., 43B, 2018 - 20 (2004).
22. Misra AK & Agnihotri G. Nitric acid mediated
oxidative transformation of thiols to disulfides. Synthetic Communications, 34, 1079 - 85 (2004).
21. Sengupta P, Misra AK, Suzuki
M, Fukuda M & Hindsgaul O. Chemoenzymatic Synthesis
Of Sialylated Oligosaccharides For Their Evaluation In A Polysialyltransferase
Assay. Tetrahedron Lett., 44, 6037 - 6042 (2003).
20. Akama
TO, Misra AK, Hindsgaul O & Fukuda MN. Enzymatic synthesis in vitro of the
Disulfated Disaccharide unit of Corneal Keratan Sulfate. J. Biol. Chem., 277, 42505 - 42513 (2002).
19. Gastinel LN, Bignon C,
Misra AK, Hindsgaul O, Shaper JH & Joziasse D. Bovine a 1, 3-galactosyl-transferase
catalytic domain structure and its relationship with ABO histo-blood group
andglycosphingolipid glycosyltransferases. EMBO J., 20, 638 - 649 (2001).
18. Hiraoka
N, Misra AK, Belot F, Hindsgaul O & Fukuda M. Molecular cloning and
expression of two distinct human N-acetylgalacto-samine 4-O-sulfotrans-ferases
that transfer sulfate to GalNAcb1-4GlcNAcb1-R in N- &
O-glycans. Glycobiology, 11, 495 - 504 (2001).
17. Misra AK, Fukuda M &
Hindsgaul O. Efficient synthesis of lactosaminylated Core-2 O-Glycans. Bioorg. Med. Chem. Lett.,
11, 2667 - 2669 (2001).
16. Misra AK, Ujita M, Fukuda M & Hindsgaul
O. Synthesis and enzymatic evaluation of mucin type core-4 O-Glycan. Carbohydr.
Lett., 4,
71 - 76 (2001).
15. Suzuki
A, Hiraoka N, Angata K, Misra AK, McAuliffe J, Hindsgaul O & Fukuda M. Molecular
cloning and expression of a novel human b-Gal-3-O-sulfotransferase that acts preferentially on
N-acetyllactosamine in N- and O-glycans. J. Biol. Chemistry, 276, 24388 - 24395 (2001).
14. Homiester JW, Thall A, Petrynaik
B, Maly P, Rogers C, Smith P, Kelly R, Gersten K, Cheng G, Marks R, Misra AK,
Hindsgaul O, Adrian UH von & Lowe JB. The a (1,3) fucosyltransferaces Fuc- TIV and Fuc-TVII co-dominantly control
selectin ligand activities on leukocytes and high endothelial venules. Immunity,
15, 115 - 126 (2001).
13. Ujita M, Misra AK, McAuliffe
J, Hindsgaul O & Fukuda M. Poly-N-acetyllactosamine extention in N-glycans
and core 2- and core 4- branch-ed O-glycans is differenti-ally controlled by
i-exten-tion enzyme and different members of the b 1, 4-galactosyltransferase gene. J. Biol. Chem., 275(21), 15868 - 15875 (2000).
12. Misra AK, Ding Y, Lowe JB & Hindsgaul
O. A concise synthesis of the 6-O and 6′-O-sulfated analogues of the sialyl
Lewis X tetrasaccharide. Bioorg. Med. Chem. Lett., 10 (14) 1505 - 1509 (2000).
11. Nakayama J, Yeh J-C,
Misra AK, Ito S, Katsuyama T & Fukuda M. Expression cloning of a human a1,
4-N-acetygluco-saminyl-transferase that forms GlcNAc a®4Galb ®R, a glycan specifically expressed in the gastric gland mucous
cell-type mucin. Proc. Natl. Acad. Sci. (PNAS) U.S.A., 6, 8991 - 8996 (1999).
10. Misra AK, Brown JM, Homans SW & Field RA. Synthesis of 13C-labelled methyl a-D-mannopyranosyl-(1®2)-a-D-mannopyrano-side from [U-13C]-D-Glucose. Carbohydr. Lett., View More
Recognition:
- Visiting scientist to University of Debrecen, Hungary under INSA-HAS bilateral exchange program (April-June 2015), 2015
- Dr. H.C. Srivastava young scientist award from Association of Carbohydrate Chemists and Technologists (India), 2014
- Visiting scientist to Abo Akademy University, Turku, Finland (Aug-Oct. 2013) under DBT, India-Academy of Finland exchange program, 2013
- Visiting scientist to University of Konstanz, Germany under INSA-DFG bilateral exchange program (March-May 2009), 2009
- DST Ramanna Research Fellowship, 2007
- CSIR Young Scientist Award in Chemical Sciences, 2005
Teaching:
PhD Course work coordinator: Structure elucidation and synthetic studies of bio-active medicinally important molecules.
Integrated MSc course: classes taken in chemistry biology course.
Students:
Image | Name | Designation | Department | Campus | Contact number | |
---|---|---|---|---|---|---|
Abhijit Rana | Junior Research Fellow | Division of Molecular Medicine | Centenary | ranaabhijit70@gmail.com | ||
Aniket Majhi | Junior Research Fellow | Chemical Sciences | Unified | majhianiket9@gmail.com | ||
Saikat Dogra | Junior Research Fellow | Chemical Sciences | Unified | saikatdogra56@gmail.com | ||
Samim Sahaji | Junior Research Fellow | Division of Molecular Medicine | Centenary | samim.sahaji98@gmail.com |
Former:
Former Group Members:
Dr. Geetanjali
Agnihotri
Dr. Pallavi Tiwari
Dr. Rishi Kumar
Dr. Soni Kamlesh Madhusudan
Dr. Chinmoy Mukherjee
Dr. Pintu Kumar Mandal
Dr. Rajib Panchadhayee
Dr. Samir Ghosh
Dr. Goutam Guchhait
Dr. Abhishek Santra
Dr. Abhijit Sau
Dr. Manas Jana
Dr. Tamashree
Ghosh
Dr. Debashis Dhara
Dr. Kobirul Islam
Dr. Utsab Debnath
Dr. Anshupriya Si
Dr. Ishani Bhaumik
Dr. Ananya Dutta
Dr. Arin Gucchait
Dr. Tapashi Manna
Dr. Pradip Shit
Monalisa Kundu
Current Group Members:
Mr. Abhijit Rana Mr. Samim Sahaji | CSIR-SRF MANF-SRF | ranaabhijit70@gmail.com samim.sahaji98@gmail.com | |
Mr. Satyajit Halder | CSIR-SRF | satyajithalder.dna@gmail.com |
Group News:
For Junior Research Fellow positions Interested candidates having M.Sc. in Organic Chemistry may directly write to me (E-mail: akmisra69@gmail.com/anup@jcbose.ac.in). The candidate should have CSIR-JRF or UGC-JRF fellowship.