The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues
- 3 September 1999
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 40 (36) , 6689-6692
- https://doi.org/10.1016/s0040-4039(99)01378-7
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Asymmetric Synthesis of (1'S,2'R)-Cyclopropyl Carbocyclic NucleosidesThe Journal of Organic Chemistry, 1995
- Synthesis of optically active cis- and trans-1,2-disubstituted cyclopropane derivatives by the Simmons-Smith reaction of allyl alcohol derivatives derived from (R)-2,3-O-isopropylideneglyceraldehydeThe Journal of Organic Chemistry, 1994
- Enzyme reactions in apolar solvent. 5. The effect of adjacent unsaturation on the porcine pancreatic lipase catalyzed kinetic resolution of secondary alcoholsThe Journal of Organic Chemistry, 1992
- An unexpected reversal of fluorine substituent effects in the biomethylenation of two positional isomers: a serendipitous discoveryThe Journal of Organic Chemistry, 1990
- An Improved Preparation of (+)2,3-O-Isopropylidene-D-GlyceraldehydeSynthetic Communications, 1988
- Determination de la configuration absolue de dialkyl-1,2 cis cyclopropanesTetrahedron, 1972
- Radiolysis of Simple Ketones1Journal of the American Chemical Society, 1958
- The Crystallography and Structure of Some C19 Cyclopropane Fatty Acids1Journal of the American Chemical Society, 1957
- On the Structure of Lactobacillic Acid1,2Journal of the American Chemical Society, 1954
- THE CHEMICAL NATURE OF A UNIQUE FATTY ACIDJournal of the American Chemical Society, 1950