Stannylene directed selective acylation of some open-chain L-arabinose derivatives

Martin W. Bredenkamp; Cedric W. Holzapfel; Anna D. Swanepoel

doi:10.1016/S0040-4039(00)94692-6

Stannylene directed selective acylation of some open-chain L-arabinose derivatives

Martin W. Bredenkamp
, Cedric W. Holzapfel
, Anna D. Swanepoel

Chemical Sciences

University of Johannesburg

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

22 Citations (Scopus)

Abstract

Controlled mono-2- or -4-acylation of open-chain L-arabinose derivatives is achieved by terminal group manipulation and dibutylstannylene oxide activation. The method was used for the preparation of a 4-mesyl-Larabinose derivative which was converted into a thioxylose synthon.

Original language	English
Pages (from-to)	2759-2762
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	19
DOIs	https://doi.org/10.1016/S0040-4039(00)94692-6
Publication status	Published - Jan 1990

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)94692-6

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title = "Stannylene directed selective acylation of some open-chain L-arabinose derivatives",

abstract = "Controlled mono-2- or -4-acylation of open-chain L-arabinose derivatives is achieved by terminal group manipulation and dibutylstannylene oxide activation. The method was used for the preparation of a 4-mesyl-Larabinose derivative which was converted into a thioxylose synthon.",

author = "Bredenkamp, \{Martin W.\} and Holzapfel, \{Cedric W.\} and Swanepoel, \{Anna D.\}",

year = "1990",

month = jan,

doi = "10.1016/S0040-4039(00)94692-6",

language = "English",

volume = "31",

pages = "2759--2762",

journal = "Tetrahedron Letters",

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publisher = "Elsevier Ltd.",

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T1 - Stannylene directed selective acylation of some open-chain L-arabinose derivatives

AU - Bredenkamp, Martin W.

AU - Holzapfel, Cedric W.

AU - Swanepoel, Anna D.

PY - 1990/1

Y1 - 1990/1

N2 - Controlled mono-2- or -4-acylation of open-chain L-arabinose derivatives is achieved by terminal group manipulation and dibutylstannylene oxide activation. The method was used for the preparation of a 4-mesyl-Larabinose derivative which was converted into a thioxylose synthon.

AB - Controlled mono-2- or -4-acylation of open-chain L-arabinose derivatives is achieved by terminal group manipulation and dibutylstannylene oxide activation. The method was used for the preparation of a 4-mesyl-Larabinose derivative which was converted into a thioxylose synthon.

UR - https://www.scopus.com/pages/publications/0025375098

U2 - 10.1016/S0040-4039(00)94692-6

DO - 10.1016/S0040-4039(00)94692-6

M3 - Article

AN - SCOPUS:0025375098

SN - 0040-4039

VL - 31

SP - 2759

EP - 2762

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 19

ER -

Stannylene directed selective acylation of some open-chain L-arabinose derivatives

Abstract

ASJC Scopus subject areas

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