Towards dideoxynucleosides: the silicon approach

Derek H.R. Barton; Doo Ok Jang; Joseph Cs Jaszberenyi

doi:10.1016/S0040-4039(00)78787-9

Towards dideoxynucleosides: the silicon approach

Derek H.R. Barton, Doo Ok Jang, Joseph Cs Jaszberenyi

Chemistry and Medical Chemistry

Research output: Contribution to journal › Article › peer-review

64 Citations (Scopus)

Abstract

Dixanthanes, formed from vic-diols, can easily be transformed to the corresponding olefins with diphenylsilane in a new, high-yielding radical reaction.

Original language	English
Pages (from-to)	2569-2572
Number of pages	4
Journal	Tetrahedron Letters
Volume	32
Issue number	23
DOIs	https://doi.org/10.1016/S0040-4039(00)78787-9
Publication status	Published - 1991 Jun 3

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)78787-9

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title = "Towards dideoxynucleosides: the silicon approach",

abstract = "Dixanthanes, formed from vic-diols, can easily be transformed to the corresponding olefins with diphenylsilane in a new, high-yielding radical reaction.",

author = "Barton, {Derek H.R.} and Jang, {Doo Ok} and Jaszberenyi, {Joseph Cs}",

year = "1991",

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T2 - the silicon approach

AU - Barton, Derek H.R.

AU - Jang, Doo Ok

AU - Jaszberenyi, Joseph Cs

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AB - Dixanthanes, formed from vic-diols, can easily be transformed to the corresponding olefins with diphenylsilane in a new, high-yielding radical reaction.

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 23

ER -

Towards dideoxynucleosides: the silicon approach

Abstract

All Science Journal Classification (ASJC) codes

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