The synthesis of single enantiomers of a meromycolic acid

JR Al Dulayymi; MS Baird; E Roberts

doi:10.1016/S0040-4039(00)01147-3

The synthesis of single enantiomers of a meromycolic acid

JR Al Dulayymi, MS Baird, E Roberts

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

Abstract

3-Oxa-2,4-dioxobicyclo[3.1.0]hexane provides a flexible starting material for the preparation of single enantiomers of a meromycolic acid, a long chain fatty acid containing two remote cis-cyclopropanes. (C) 2000 Elsevier Science Ltd. All rights reserved.

Original language	English
Pages (from-to)	7107-7110
Number of pages	4
Journal	Tetrahedron Letters
Volume	41
Issue number	36
DOIs	https://doi.org/10.1016/S0040-4039(00)01147-3
Publication status	Published - 2 Sept 2000

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title = "The synthesis of single enantiomers of a meromycolic acid",

abstract = "3-Oxa-2,4-dioxobicyclo[3.1.0]hexane provides a flexible starting material for the preparation of single enantiomers of a meromycolic acid, a long chain fatty acid containing two remote cis-cyclopropanes. (C) 2000 Elsevier Science Ltd. All rights reserved.",

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T1 - The synthesis of single enantiomers of a meromycolic acid

AU - Al Dulayymi, JR

AU - Baird, MS

AU - Roberts, E

PY - 2000/9/2

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N2 - 3-Oxa-2,4-dioxobicyclo[3.1.0]hexane provides a flexible starting material for the preparation of single enantiomers of a meromycolic acid, a long chain fatty acid containing two remote cis-cyclopropanes. (C) 2000 Elsevier Science Ltd. All rights reserved.

AB - 3-Oxa-2,4-dioxobicyclo[3.1.0]hexane provides a flexible starting material for the preparation of single enantiomers of a meromycolic acid, a long chain fatty acid containing two remote cis-cyclopropanes. (C) 2000 Elsevier Science Ltd. All rights reserved.

U2 - 10.1016/S0040-4039(00)01147-3

DO - 10.1016/S0040-4039(00)01147-3

M3 - Article

SN - 0040-4039

VL - 41

SP - 7107

EP - 7110

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 36

ER -

The synthesis of single enantiomers of a meromycolic acid

Abstract

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