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Sachin G. Deshpande

Researcher at National Chemical Laboratory

Publications -  8
Citations -  43

Sachin G. Deshpande is an academic researcher from National Chemical Laboratory. The author has contributed to research in topics: Michael reaction & Nucleophile. The author has an hindex of 4, co-authored 8 publications receiving 42 citations.

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Vinylsulfone-modified carbohydrates: first general route to d-lividosamine (2-amino-2,3-dideoxy-d-glucose) and its new analogues

TL;DR: In this article, a diastereoselective introduction of N-monoalkylated and N-dialkylated amines to C-2 carbons of methyl 2,3-dideoxy-3-C-phenylsulfonyl-α-d -hex-hex-2-enopyranoside has been devised for the first time.
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Synthesis and synthetic applications of 1-(3-O-tosyl-β-d-glucopyranosyl) thymines: toward new classes of hexopyranosyl pyrimidines

TL;DR: The availability of this key nucleoside made possible the synthesis of a wide range of modified hexopyranosyl nucleosides can be easily prepared from these functionalized starting materials.
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A general and efficient route to 3′-deoxy-3′-N-, S-, and C-substituted altropyranosyl thymines from 2′,3′-O-anhydro-mannopyranosylthymine

TL;DR: In this paper, an efficient route to 1-(2,3- O -anhydro-4,6-O -phenylmethylene-β- d -mannopyranosyl) from 1,2,4, 6-tetra-acetyl-3, O -tosyl-β-, d -glucopyranose has been devised.
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Studies on the synthesis and unusual behavior of vinyl sulfone-modified hexenopyranosylthymines

TL;DR: Although vinyl sulfone-modified- (VSM) pent-2'-enofuranosyl nucleosides 2 and hex-2-enopyranosyl glycoside 4 are easily synthesized from the corresponding mesylated sulfones 1c and 3c, via an oxidation-mesylation-elimination route, the 3'-C-sulfonyl-hex-3'-enopyrsylthymine 11 is not obtained from 10 and a glycal