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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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Currently
supervising eight research students for their Ph D degree |
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| SELECTED
PUBLICATIONS |
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“Studies on Tetrahydrofuran
based highly O-Functionalized Alkynes: Applications to
Synthesis of Tetrahydrofuran Symmetrical, Unsymmetrical
Polyynes and C nucleoside analogues” P. Venkat Reddy,
V. Bajpai, B. Kumar, A. K. Shaw. Accepted
Article. Eur. J. Org. Chem. 2011 |
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“A Convergent Total
Synthesis of a New Antiepileptic Ceramide and its Triacetyl
Derivative Using Olefin Cross Metathesis” Partha
Ghosal, Vikas Kumar and Arun K. Shaw Tetrahedron
2010, 66, 7504-7509. |
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“An efficient total
synthesis of the anticancer agent (+)-spisulosine (ES-285)
from Garner’s aldehyde” Partha Ghosal, Arun
K. Shaw* Tetrahedron Letters 2010, 51, 4140-4142. |
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“Synthesis and biological
evaluation of glycal-derived novel tetrahydrofuran 1,2,3-triazoles
by ‘click’ chemistry” L. Vijaya Raghava
Reddy, P. Venkat Reddy, Nripendra N. Mishra, Praveen K.
Shukla, Garima Yadav, Ranjana Srivastava, Arun
K. Shaw, Carbohydrate Research 2010, 345 ,1515-1521
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“A chiron approach
to the total synthesis of cytotoxic (+)-muricatacin and
(+)-5-epi- muricatacin from D-ribose” P. Ghosal,
V. Kumar, A. K. Shaw Carbohydrate Research 2010,
345, 41-44. |
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“Facile Synthesis
of Enantiomerically Pure 2- and 2,3-Disubstituted Furans
Catalysed by Mixed Lewis Acids: An Easy Route to 3-Iodofurans
and 3-(Hydroxymethyl)furans” M. Saquib, I. Husain,
B. Kumar, A. K. Shaw Chem. Eur. J. 2009,
15, 6041-6049. |
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“Synthesis of enantiomerically
pure highly functionalized furanoid glycals and 2,5-dihydrofurans
building blocks” P. Pal, B. Kumar, A. K.
Shaw Eur. J. Org. Chem. 2009, 2179-2184. |
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Kumar Vikas and Shaw
Arun K - First total synthesis of (+)-Varitriol
(2008) - J. Org. Chemistry 73, 7526-7531
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Reddy L Vijaya Raghava,
Swamy G Narayana and Shaw Arun K - A
versatile route for the stereoselective synthesis of oxybiotin.
(2008) - Tetrahedron Asymmetry 19, 1372-1375
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Reddy P Venkat, Reddy
L Vijaya, Raghava, Kumar Brijesh, Kumar Rishi, Maulik
Prakas R and Shaw Arun K. - A general
and efficient stereoselective synthesis of ?-azido-tetrahydrofuran
carboxylic acids from glycals (2008) - Tetrahedron
64, 2153-2159 |
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Kumar Vikas, Gauniyal
Harsh Mohan and Shaw Arun K. - An iodocyclization
approach toward diastereoselective synthesis of highly
functionalized tetrasubstituted tetrahydrofurans with
2,5-trans and 2,5-cis relationships from pyranoside derived
acyclic oximes. (2007) - Tetrahedron Asymmetry
18, 2069-2078 |
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Reddy L Vijaya Raghava,
Reddy Venkat P and Shaw Arun K - An expedient
route for the practical synthesis of pachastrissamine
(jaspine B) starting from 3,4,6-tri-O-benzyl-d-galactal.
(2007) - Tetrahedron Asymmetry 18, 542-546
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Saquib M, Gupta MK, Sagar
R, Prabhakar YS, Shaw AK, Kumar R, Maulik
PR, Gaikwad AN, Sinha S, Srivastava AK, Chaturvedi V,
Srivastava R and Srivastava BS - C-3 alkyl/arylalkyl-2,3-dideoxy
hex-2-enopyranosides as antitubercular agents: Synthesis,
biological evaluation, and QSAR study. (2007)
- Journal of Medicinal Chemistry 50, 2942-2950
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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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