𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Enantioselective Protonation of a Lithium Enolate Derived from 2-Methyl-1-tetralone Using Chiral Sulfonamides.

✍ Scribed by Gregory S. Coumbarides; Jason Eames; J. Erik W. Scheuermann; Kevin F. Sibbons; Michael J. Suggate; Michael Watkinson

Publisher
John Wiley and Sons
Year
2005
Weight
19 KB
Volume
36
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Diastereoselective
ChemInform Abstract: Diastereoselective Protonation of Chiral Enolates Derived from 2,4-Dimethyl-1-tetralone Using Carbonyl Chelating Proton Donors.
✍ Jason Eames πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 25 KB

## 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 v

ChemInform Abstract: Chiral Aminoborane
ChemInform Abstract: Chiral Aminoborane as a Chiral Proton Source for Asymmetric Protonation of Lithium Enolates Derived from 2-Arylcyloalkanones.
✍ A. YANAGISAWA; H. INANAMI; H. YAMAMOTO πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 2 views

1998 stereochemistry stereochemistry (general, optical resolution) O 0030 ## 47 -038 Chiral Aminoborane as a Chiral Proton Source for Asymmetric Protonation of Lithium Enolates Derived from 2-Arylcyloalkanones. -The first example of asymmetric protonation using a metal-containing chiral proton so