Iodoetherification of homoallylic alcohols : a stereoselective approach to tetrahydrofurans

Simon B. Bedford; Kathryn E. Bell; Garry Fenton; Christopher J. Hayes; David W. Knight; Duncan Shaw

doi:10.1016/S0040-4039(00)79029-0

Iodoetherification of homoallylic alcohols : a stereoselective approach to tetrahydrofurans

Simon B. Bedford
, Kathryn E. Bell
, Garry Fenton
, Christopher J. Hayes
, David W. Knight
, Duncan Shaw

Western Sydney University

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

48 Citations (Scopus)

Abstract

Iodoetherification of homoallylic alcohols proceeds efficiently and with high levels of stereoselection by a 5-endo-trig process when anhydrous acetonitrile is used as the solvent.

Original language	English
Pages (from-to)	6511-6514
Number of pages	4
Journal	Tetrahedron Letters
Volume	33
Issue number	43
DOIs	https://doi.org/10.1016/S0040-4039(00)79029-0
Publication status	Published - 1992

Keywords

allyl alcohol

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10.1016/S0040-4039(00)79029-0

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@article{e530e8887d044ac2a563bbac5151bcac,

title = "Iodoetherification of homoallylic alcohols : a stereoselective approach to tetrahydrofurans",

abstract = "Iodoetherification of homoallylic alcohols proceeds efficiently and with high levels of stereoselection by a 5-endo-trig process when anhydrous acetonitrile is used as the solvent.",

keywords = "allyl alcohol",

author = "Bedford, \{Simon B.\} and Bell, \{Kathryn E.\} and Garry Fenton and Hayes, \{Christopher J.\} and Knight, \{David W.\} and Duncan Shaw",

year = "1992",

doi = "10.1016/S0040-4039(00)79029-0",

language = "English",

volume = "33",

pages = "6511--6514",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd.",

number = "43",

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TY - JOUR

T1 - Iodoetherification of homoallylic alcohols : a stereoselective approach to tetrahydrofurans

AU - Bedford, Simon B.

AU - Bell, Kathryn E.

AU - Fenton, Garry

AU - Hayes, Christopher J.

AU - Knight, David W.

AU - Shaw, Duncan

PY - 1992

Y1 - 1992

N2 - Iodoetherification of homoallylic alcohols proceeds efficiently and with high levels of stereoselection by a 5-endo-trig process when anhydrous acetonitrile is used as the solvent.

AB - Iodoetherification of homoallylic alcohols proceeds efficiently and with high levels of stereoselection by a 5-endo-trig process when anhydrous acetonitrile is used as the solvent.

KW - allyl alcohol

UR - http://handle.westernsydney.edu.au:8081/1959.7/uws:47674

U2 - 10.1016/S0040-4039(00)79029-0

DO - 10.1016/S0040-4039(00)79029-0

M3 - Article

SN - 0040-4039

VL - 33

SP - 6511

EP - 6514

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 43

ER -

Iodoetherification of homoallylic alcohols : a stereoselective approach to tetrahydrofurans

Abstract

Keywords

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