A Ramberg-Backlund approach to exo-glycals

Frank K. Griffin; Paul V. Murphy; Duncan E. Paterson; Richard J.K. Taylor

doi:10.1016/S0040-4039(98)01822-X

A Ramberg-Backlund approach to exo-glycals

Frank K. Griffin, Paul V. Murphy, Duncan E. Paterson, Richard J.K. Taylor

Research output: Contribution to a Journal (Peer & Non Peer) › Article › peer-review

68 Citations (Scopus)

Abstract

A new route to exo-glycals is described which starts from S-glycoside dioxides and utilises Meyers' variant of the Ramberg-Backlund rearrangement. The methodology is successful with glucose, galactose, mannose, xylose, fucose and ribose derivatives, and has been used to prepare di-, tri- and tetra-substituted alkenes.

Original language	English
Pages (from-to)	8179-8182
Number of pages	4
Journal	Tetrahedron Letters
Volume	39
Issue number	44
DOIs	https://doi.org/10.1016/S0040-4039(98)01822-X
Publication status	Published - 29 Oct 1998
Externally published	Yes

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10.1016/S0040-4039(98)01822-X

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title = "A Ramberg-Backlund approach to exo-glycals",

abstract = "A new route to exo-glycals is described which starts from S-glycoside dioxides and utilises Meyers' variant of the Ramberg-Backlund rearrangement. The methodology is successful with glucose, galactose, mannose, xylose, fucose and ribose derivatives, and has been used to prepare di-, tri- and tetra-substituted alkenes.",

author = "Griffin, \{Frank K.\} and Murphy, \{Paul V.\} and Paterson, \{Duncan E.\} and Taylor, \{Richard J.K.\}",

year = "1998",

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doi = "10.1016/S0040-4039(98)01822-X",

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T1 - A Ramberg-Backlund approach to exo-glycals

AU - Griffin, Frank K.

AU - Murphy, Paul V.

AU - Paterson, Duncan E.

AU - Taylor, Richard J.K.

PY - 1998/10/29

Y1 - 1998/10/29

N2 - A new route to exo-glycals is described which starts from S-glycoside dioxides and utilises Meyers' variant of the Ramberg-Backlund rearrangement. The methodology is successful with glucose, galactose, mannose, xylose, fucose and ribose derivatives, and has been used to prepare di-, tri- and tetra-substituted alkenes.

AB - A new route to exo-glycals is described which starts from S-glycoside dioxides and utilises Meyers' variant of the Ramberg-Backlund rearrangement. The methodology is successful with glucose, galactose, mannose, xylose, fucose and ribose derivatives, and has been used to prepare di-, tri- and tetra-substituted alkenes.

UR - https://www.scopus.com/pages/publications/0032578741

U2 - 10.1016/S0040-4039(98)01822-X

DO - 10.1016/S0040-4039(98)01822-X

M3 - Article

SN - 0040-4039

VL - 39

SP - 8179

EP - 8182

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 44

ER -

A Ramberg-Backlund approach to exo-glycals

Abstract

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