๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Highly Diastereoselective Radical Addition to Glyoxylate Imines of Chiral Amines without Additional Heteroatoms.

โœ Scribed by Nishan Singh; R. D. Anand; Sanjay Trehan


Publisher
John Wiley and Sons
Year
2004
Weight
142 KB
Volume
35
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

For Abstract see ChemInform Abstract in Full Text.


๐Ÿ“œ SIMILAR VOLUMES


Highly diastereoselective addition of si
โœ Hiroshi Shinokubo; Junichi Kondo; Atsushi Inoue; Koichiro Oshima ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 122 KB ๐Ÿ‘ 1 views

Treatment of benzoate, formate, or trifluoroacetate esters with silyldibromomethyllithiums provides alkyl silyl mixed acetals via the 1,3-rearrangement of a silyl group from carbon to oxygen. A high level of asymmetric induction onto the acetal carbon is observed when chiral alkyl esters are employe

ChemInform Abstract: Highly Diastereosel
โœ N. MASE; Y. WATANABE; Y. UENO; T. TORU ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 43 KB ๐Ÿ‘ 1 views

Highly Diastereoselective Intermolecular ฮฒ-Addition of Alkyl Radicals to Chiral 2-(Arylsulfinyl)-2-cycloalkenones. -The reaction of cycloalkenones having chiral bulky arylsulfinyl groups proceeds with excellent diastereoselectivity. In the presence of the Lewis acids EtAlCl 2 and TiCl 2 (OiPr) 2 re