A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones

Michael T. Crimmins; Caroline J. Diaz; Kyle A. Emmitte

A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones

Michael T. Crimmins, Caroline J. Diaz, Kyle A. Emmitte

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

Abstract

A stereoselective construction of cis- and trans-2,6-disubstituted tetrahydropyranones, based on strategy which combines an asymmetric alkylation and ring closing metathesis for the formation of a cyclic enol ether, is reported.

Original language	English
Pages (from-to)	179-183
Number of pages	5
Journal	Heterocycles
Volume	62
State	Published - 1 Jan 2004

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title = "A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones",

abstract = "A stereoselective construction of cis- and trans-2,6-disubstituted tetrahydropyranones, based on strategy which combines an asymmetric alkylation and ring closing metathesis for the formation of a cyclic enol ether, is reported.",

author = "Crimmins, {Michael T.} and Diaz, {Caroline J.} and Emmitte, {Kyle A.}",

year = "2004",

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language = "English",

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T1 - A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones

AU - Crimmins, Michael T.

AU - Diaz, Caroline J.

AU - Emmitte, Kyle A.

PY - 2004/1/1

Y1 - 2004/1/1

N2 - A stereoselective construction of cis- and trans-2,6-disubstituted tetrahydropyranones, based on strategy which combines an asymmetric alkylation and ring closing metathesis for the formation of a cyclic enol ether, is reported.

AB - A stereoselective construction of cis- and trans-2,6-disubstituted tetrahydropyranones, based on strategy which combines an asymmetric alkylation and ring closing metathesis for the formation of a cyclic enol ether, is reported.

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M3 - Article

AN - SCOPUS:0346459968

SN - 0385-5414

VL - 62

SP - 179

EP - 183

JO - Heterocycles

JF - Heterocycles

ER -

A unified approach to the enantioselective synthesis of 2,6-cis and trans disubstituted tetrahydropyranones

Abstract

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