Cis-epoxides via sharpless' asymmetric dihydroxylation reaction: Synthesis of (+)-disparlure

Soo Y. Ko

doi:10.1016/S0040-4039(00)73251-5

Cis-epoxides via sharpless' asymmetric dihydroxylation reaction: Synthesis of (+)-disparlure

Soo Y. Ko

Department of Chemistry & Nanoscience

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

27 Scopus citations

Abstract

(+)-Disparlure, containing an isolated cis-epoxide functional group, was synthesized employing the asymmetric dihydroxylation and cyclic sulfate rearrangement-opening reactions as the key steps.

Original language	English
Pages (from-to)	3601-3604
Number of pages	4
Journal	Tetrahedron Letters
Volume	35
Issue number	21
DOIs	https://doi.org/10.1016/S0040-4039(00)73251-5
State	Published - 23 May 1994

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title = "Cis-epoxides via sharpless' asymmetric dihydroxylation reaction: Synthesis of (+)-disparlure",

abstract = "(+)-Disparlure, containing an isolated cis-epoxide functional group, was synthesized employing the asymmetric dihydroxylation and cyclic sulfate rearrangement-opening reactions as the key steps.",

author = "Ko, {Soo Y.}",

year = "1994",

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T1 - Cis-epoxides via sharpless' asymmetric dihydroxylation reaction

T2 - Synthesis of (+)-disparlure

AU - Ko, Soo Y.

PY - 1994/5/23

Y1 - 1994/5/23

N2 - (+)-Disparlure, containing an isolated cis-epoxide functional group, was synthesized employing the asymmetric dihydroxylation and cyclic sulfate rearrangement-opening reactions as the key steps.

AB - (+)-Disparlure, containing an isolated cis-epoxide functional group, was synthesized employing the asymmetric dihydroxylation and cyclic sulfate rearrangement-opening reactions as the key steps.

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U2 - 10.1016/S0040-4039(00)73251-5

DO - 10.1016/S0040-4039(00)73251-5

M3 - Article

AN - SCOPUS:0028277875

SN - 0040-4039

VL - 35

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EP - 3604

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 21

ER -

Cis-epoxides via sharpless' asymmetric dihydroxylation reaction: Synthesis of (+)-disparlure

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