Diastereoselective synthesis of optically active (2R,5R)-hexanediol
β Scribed by J. Haberland, A. Kriegesmann, E. Wolfram, W. Hummel, A. Liese
- Book ID
- 105949058
- Publisher
- Springer
- Year
- 2002
- Tongue
- English
- Weight
- 152 KB
- Volume
- 58
- Category
- Article
- ISSN
- 1432-0614
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A stereospecific synthesis of (R,R)-phytol with highZy stereochemical purity in both absolute and geometrical configurations was aehieved by utiZi,zing the 5~2 type ring-opening reaction of CR)-B-methyZ-fkpropiolactone, and the SLv2' type ring-opening reaction of isopropenyl oxirane, from CR)-pdegon
## Abstract The following compounds were identified as male pheromone components of the longhorn beetles __Hylotrupes bajulus__ and __Pyrrhidium sanguineum__: (3__R__)β3βhydroxyβ2βhexanone [(3__R__)β1], (2__S__,3__R__)β2,3βhexanediol [(2__S__,3__R__)β4] and (2__R__,3__R__)β2,3βhexanediol [(2__R__,3
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.