Stereochemical features of iodocyclisations of 3-alkene-1,2-diols to beta-hydroxytetrahydrofurans

Sean P. Bew; Jenny M. Barks; David W. Knight; Robert J. Middleton

doi:10.1016/S0040-4039(00)00613-4

Stereochemical features of iodocyclisations of 3-alkene-1,2-diols to beta-hydroxytetrahydrofurans

Sean P. Bew, Jenny M. Barks, David W. Knight, Robert J. Middleton

Chemistry of Materials and Catalysis

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

Abstract

5-endo-Iodocyclisations of stereoisomers of 3-alkene-1,2-diols 9, 12, 15 and 18 are stereoselective and provide an efficient route to beta-hydroxytetrahydrofurans. (C) 2000 Elsevier Science Ltd. All rights reserved.

Original language	English
Pages (from-to)	4447-4451
Number of pages	5
Journal	Tetrahedron Letters
Volume	41
Issue number	22
DOIs	https://doi.org/10.1016/S0040-4039(00)00613-4
Publication status	Published - 2000

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10.1016/S0040-4039(00)00613-4

Cite this

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title = "Stereochemical features of iodocyclisations of 3-alkene-1,2-diols to beta-hydroxytetrahydrofurans",

abstract = "5-endo-Iodocyclisations of stereoisomers of 3-alkene-1,2-diols 9, 12, 15 and 18 are stereoselective and provide an efficient route to beta-hydroxytetrahydrofurans. (C) 2000 Elsevier Science Ltd. All rights reserved.",

author = "Bew, {Sean P.} and Barks, {Jenny M.} and Knight, {David W.} and Middleton, {Robert J.}",

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AU - Bew, Sean P.

AU - Barks, Jenny M.

AU - Knight, David W.

AU - Middleton, Robert J.

PY - 2000

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AB - 5-endo-Iodocyclisations of stereoisomers of 3-alkene-1,2-diols 9, 12, 15 and 18 are stereoselective and provide an efficient route to beta-hydroxytetrahydrofurans. (C) 2000 Elsevier Science Ltd. All rights reserved.

U2 - 10.1016/S0040-4039(00)00613-4

DO - 10.1016/S0040-4039(00)00613-4

M3 - Article

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

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