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
โฆ LIBER โฆ
Highly Diastereoselective Radical Addition to Glyoxylate Imines of Chiral Amines without Additional Heteroatoms.
โ 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.
โฆ Synopsis
Abstract
For Abstract see ChemInform Abstract in Full Text.
๐ SIMILAR VOLUMES
Highly diastereoselective addition of si
โ
Hiroshi Shinokubo; Junichi Kondo; Atsushi Inoue; Koichiro Oshima
๐
Article
๐
2002
๐
John Wiley and Sons
๐
English
โ 122 KB
๐ 1 views
ChemInform Abstract: Highly Diastereosel
โ
H. MIYABE; C. USHIRO; T. NAITO
๐
Article
๐
2010
๐
John Wiley and Sons
โ 32 KB
๐ 2 views
Highly Diastereoselective Conjugate Addi
โ
Jesse Dambacher; Robert Anness; Patrick Pollock; Mikael Bergdahl
๐
Article
๐
2004
๐
John Wiley and Sons
โ 276 KB
๐ 1 views
ChemInform Abstract: Asymmetric Synthesi
โ
Derek A. Cogan; Guangcheng Liu; Jonathan Ellman
๐
Article
๐
2010
๐
John Wiley and Sons
โ 42 KB
๐ 2 views
ChemInform Abstract: Highly Diastereosel
โ
N. MASE; Y. WATANABE; Y. UENO; T. TORU
๐
Article
๐
2010
๐
John Wiley and Sons
โ 43 KB
๐ 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
ChemInform Abstract: Highly Diastereosel
โ
Guillaume Dunet; Peter Mayer; Paul Knochel
๐
Article
๐
2008
๐
John Wiley and Sons
โ 80 KB
๐ 1 views