Enantioselective hydride abstraction in organic substrate: A novel use forchiral carbenium ions

Citation
D. Magdziak et al., Enantioselective hydride abstraction in organic substrate: A novel use forchiral carbenium ions, ORG LETT, 3(4), 2001, pp. 557-559
Citations number
36
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
4
Year of publication
2001
Pages
557 - 559
Database
ISI
SICI code
1523-7060(20010222)3:4<557:EHAIOS>2.0.ZU;2-8
Abstract
It is surprising that chiral cations have not been used to distinguish betw een prochiral hydrides when converse notions, such as asymmetric addition o f a hyride to a prochiral functional group or use of a chiral anion to dist inghish between a pair of prochiral protons, are methods employed everyday in enantioselective synthesis. To the best of our knowledge, this Letter de scribes the first example ol an oxidative enantioselective hydride transfer process.