𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Enantioselective Protonation of Prochiral Enolates with Chiral Imides.

✍ Scribed by A. YANAGISAWA; T. KIKUCHI; T. KURIBAYASHI; H. YAMAMOTO


Publisher
John Wiley and Sons
Year
2010
Weight
40 KB
Volume
29
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis


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 β€œFull Text” option. The original article is trackable via the β€œReferences” option.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Diastereoselective
✍ A. YANAGISAWA; T. WATANABE; T. KIKUCHI; T. KURIBAYASHI; H. YAMAMOTO πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 27 KB πŸ‘ 1 views

Diastereoselective Protonation of Chiral Enolate with Chiral Imides. -Protonation of the lithium enolate (I) of (-)-menthone by chiral imides such as the (R)-imide of conditions (A) generates mainly the cis ketone (III). The selectivity of this process can be completely reversed by using the corres

Enantioselective Protonation of Simple E
✍ Dr. Akira Yanagisawa; Takeshi Kuribayashi; Tetsuo Kikuchi; Prof. Hisashi Yamamot πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 411 KB πŸ‘ 1 views

Dimeric [Ca(OCtBu,) ,] is synthesized from 2a and HOCIBU, by analogy to Equation (c); colorless crystals, moderately soluble in n-pentane. readily soluble in toluene and diethyl ether. Warming under high vacuum (185'Ci mbar) gives a moderate yield of trimeric [Ca(OCHtBu,),] as a colorless sublimate