ChemInform Abstract: The Stereoselective Total Synthesis of (1S,1′R,5′R,7′R)-1-Hydroxy-exo-brevicomin (V) by a Chiron Approach.
✍ Scribed by Jhillu S. Yadav; Kodepelly Sanjeeva Rao; Basi V. Subba Reddy
- Publisher
- John Wiley and Sons
- Year
- 2009
- Weight
- 26 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Pheromone Synthesis. Part 183. Synthesis of (1R,2R,5S,7R)-and (1R,2S, 5S,7R)-2-Hydroxy-exo-brevicomin, the Components of the Male-Produced Volatiles of the Mountain Pine Beetle, Dendroctonus ponderosae. -Both title compounds (V) and (VI) are synthesized via asymmetric dihydroxylation as the key ste
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Two components [2-sec-butyl-4,5-dihydrothiazole (1) and were obtained with an enantiomeric purity of ca. 92% ee and were found to be readily racemizable. Asymmetric 3,4-dehydro-exo-brevicomin (2)] of a male-produced pheromone of the mouse Mus musculus have been dihydroxylation was employed as the ke