The synthesis of single enantiomers of a meromycolic acid
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In: Tetrahedron Letters, Vol. 41, No. 36, 02.09.2000, p. 7107-7110.
Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - The synthesis of single enantiomers of a meromycolic acid
AU - Al Dulayymi, JR
AU - Baird, MS
AU - Roberts, E
PY - 2000/9/2
Y1 - 2000/9/2
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
VL - 41
SP - 7107
EP - 7110
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 36
ER -