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Dr. ARUN KUMAR SHAW |
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Scientist
E II
Medicinal and Process Chemistry Division
Central Drug Research Institute
Lucknow-226001, India
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| Educational qualifications |
M.Sc. Ph.D. |
| Date of Birth |
July 07, 1955. |
| Phone Nos. |
+91-0522-2612411-18-Ext
4334, Mobile + 9415403775 |
| Fax No. |
+91-0522-2623405 |
| E- mail |
akshaw55[at]yahoo dot com |
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| RESEARCH
EXPERIENCE |
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Natural
Products Chemistry (25 years), Synthetic
Organic Chemistry (18 years), Medicinal
Chemistry (14 years). |
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| POST
DOCTORAL RESEARCH |
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CSIR-DAAD
Visiting Scientist, University of Rostock, Germany, April-June
2000 |
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| CURRENT
AREAS OF RESEARCH |
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Design, Synthesis
& Development of Target- based Anti-tubercular agents |
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Synthetic
Carbohydrate & Natural Products Chemistry |
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| GROUP
MEMBERS |
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Supervising
three research students for their Ph D degree |
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| SELECTED
PUBLICATIONS |
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Stereoselective synthesis
of highly O-functionalized enantiopure 2,3,4- trisubstituted
tetrahydrofurans by tandem debenzylative cyclization of
glycal derived 2,3-epoxy alcohols. L. Vijaya Raghava Reddy,
Abhijeet Deb Roy, Raja Roy and Arun K. Shaw.
Chem. Commun. 2006, 3444-3446. |
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Studies on epoxidation
of enantiomerically pure 2,3-dideoxy hex-2-enitols: a
convenient access to highly functionalized enantiomerically
pure tetrahydrofuran derivatives. Ram Sagar, L. Vijaya
Raghava Reddy and Arun K. Shaw. Tetrahedron: Asymmetry
2006, 17, 1189-1198. |
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An efficient synthesis
of 2,3-dideoxy-?,ß-unsaturated carbohydrate enals
by mixed Lewis acid (HfCl4 and ZnI2) catalyzed hydration
of glycals. Mohammad Saquib, Ram Sagar, Arun K.
Shaw. Carbohydr. Res. 2006, 341, 1052-1056. |
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Reductive opening of glycal
derived highly functionalized 2,3-epoxy-1-iodides with
zinc dust: an efficient method for the synthesis of acyclic
long chain polyhydroxylated terminal alkenic alcohols.
L.Vijaya Raghava Reddy, Ram Sagar, Arun. K. Shaw.
Tetrahedron Lett. 2006, 47, 1753-1756. |
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Neridienone A, a pregnane
from the roots of Nerium oleander. Rishi Kumar, Ram Sagar,
Arun. K. Shaw, Prakas. R. Maulik. Acta
Cryst. 2005, E61, o3905-o3907. |
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CP-MLR directed
QSAR studies on the antimycobacterial activity of functionalized
alkenols-topological descriptors in modeling the activity.
Manish K. Gupta, Ram Sagar, Arun K. Shaw and Yenamandra
S. Prabhakar* Bioorganic & Medicinal Chemistry (2005),
13, 343-351 |
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Diastereoselective
annulation of 4-hydroxypyran-2H-ones with enantiopure
2,3-dideoxy- -unsaturated sugar aldehydes derived from
respective glycals. Ram Sagar, Pushpa Singh, Rishi Kumar,
Prakas R. Maulik and Arun K. Shaw* Carbohydrate
Research (2005), 340, 1287-1300 |
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A convenient
approach towards separation and identification of triterpenes
of delta12 lupane series. Ram Sagar, Namrata Dilip Dhoke
and Arun K Shaw. Indian Journal
Chem Sec. B, (2004), 43B,
2446-2451. |
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Substrate
Controlled A Very High Diastereoselective Mortia-Baylis-Hillman
Reaction: A Remote Activation on the Diastereoface Selectivity
in Synthesis of C-3-Branched Deoxysugars. Ram Sagar, C.S.
Pant and R. Pathak and A.K. Shaw. Tetrahedron
(2004), 60, 11399-11406. |
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Reinvestigation
of the mercuration–demercuration reaction on alkylated
glycals: an improved method for the preparation of 2,3-dideoxy-alpha,
beta-unsaturated carbohydrate enals. Ram Sagar, Rashmi
Pathak and Arun K. Shaw. Carbohydrate
Research (2004), 339, 2031-2035. |
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A Common
Sugar as Model for Many - sided Natural Product Modification.
From D - Fructose via D - Tagatose to 2 - Difluoro - chloromethylated
D - Arabinohexopyranos - 5 - ulose Derivatives, R. Miethchen,
S. Tews, A. K. Shaw, S. Röttger,
H. Reinke. J. Carbohydr. Chem.(2004),
23, 147- 161. |
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| PATENT
FILED |
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Novel series
of unsaturated C-3 aryl and alkyl substituted 2,3- dideoxy
glucopyranosides as potential anti-tubercular agents.
Ram Sagar, Mohd Saquib, Arun K Shaw, Anil N Gaikwad,
Sudhir K Sinha, Anil Srivastava, Vinita Chaturvedi, Manju
Y K, Ranjana Srivastava and B S Srivastava. |
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