The high level of stereochemical control exhibited in the Sharpless epoxidation of prochiral divinyl alcohols has been exploited in short enantioselective syntheses of the dideoxy sugars D-digitoxose and D-olivose. ## Recent communications have reported that the Sharpless epoxidation of prochiral
β¦ LIBER β¦
The asymmetric epoxidation of divinyl carbinols: theory and applications
β Scribed by David B. Smith; Wang Zhaoyin; Stuart L. Schreiber
- Book ID
- 104203390
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 967 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Asymmetric epoxidation of divinyl carbin
β
Robert E. Babine
π
Article
π
1986
π
Elsevier Science
π
French
β 286 KB
Asymmetric concave gratings: Theory and
β
LavollΓ©e, M.; Robin, S.
π
Article
π
1974
π
Optical Society of America
β 537 KB
ChemInform Abstract: Organocatalytic Oxi
β
Yian Shi
π
Article
π
2011
π
John Wiley and Sons
β 18 KB
π 1 views
Symmetric and Asymmetric Theory of Relat
β
Leo Egghe; Ronald Rousseau
π
Article
π
2001
π
Springer Netherlands
π
English
β 160 KB
ChemInform Abstract: Asymmetric Epoxidat
β
T. KATSUKI; V. S. MARTIN
π
Article
π
2010
π
John Wiley and Sons
β 24 KB
Molecular engineering of epoxide hydrola
β
Eun Yeol Lee; Michael L. Shuler
π
Article
π
2007
π
John Wiley and Sons
π
English
β 198 KB
## Abstract Safety and regulatory issues favor increasing use of enantiopure compounds in pharmaceuticals. Enantiopure epoxides and diols are valuable intermediates in organic synthesis for the production of optically active pharmaceuticals. Enantiopure epoxide can be prepared using epoxide hydrola