Enantioselective synthesis of goniobutenolides A and B

Soo Y. Ko; Joanne Lerpiniere

doi:10.1016/0040-4039(95)00166-A

Enantioselective synthesis of goniobutenolides A and B

Soo Y. Ko, Joanne Lerpiniere

Department of Chemistry & Nanoscience

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

38 Scopus citations

Abstract

Goniobutenolides A and B were synthesized in the enantiopure forms, employing the asymmetric dihydroxylation and cyclic sulfate rearrangement-opening reactions as the key stereocenter-forming steps.

Original language	English
Pages (from-to)	2101-2104
Number of pages	4
Journal	Tetrahedron Letters
Volume	36
Issue number	12
DOIs	https://doi.org/10.1016/0040-4039(95)00166-A
State	Published - 20 Mar 1995

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title = "Enantioselective synthesis of goniobutenolides A and B",

abstract = "Goniobutenolides A and B were synthesized in the enantiopure forms, employing the asymmetric dihydroxylation and cyclic sulfate rearrangement-opening reactions as the key stereocenter-forming steps.",

author = "Ko, {Soo Y.} and Joanne Lerpiniere",

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AU - Lerpiniere, Joanne

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N2 - Goniobutenolides A and B were synthesized in the enantiopure forms, employing the asymmetric dihydroxylation and cyclic sulfate rearrangement-opening reactions as the key stereocenter-forming steps.

AB - Goniobutenolides A and B were synthesized in the enantiopure forms, employing the asymmetric dihydroxylation and cyclic sulfate rearrangement-opening reactions as the key stereocenter-forming steps.

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JO - Tetrahedron Letters

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ER -

Enantioselective synthesis of goniobutenolides A and B

Abstract

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