๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Direct formation of highly functionalized allylic organocopper reagents from allylic chlorides and acetates

โœ Scribed by Stack, Douglas E.; Dawson, Bryan T.; Rieke, Reuben D.


Book ID
126082447
Publisher
American Chemical Society
Year
1992
Tongue
English
Weight
948 KB
Volume
114
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Direct formation of functionalized keton
โœ Richard M. Wehmeyer; Reuben D. Rieke ๐Ÿ“‚ Article ๐Ÿ“… 1988 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 303 KB

Highly reactive copper solutions have been prepared by the lithium naphthalide reduction of a copper(I) iodide/triphenyl-phosphine complex. These copper solutions react rapidly with functionalized alkyl halides to give organocopper reagents which have been effectively trapped with acid chlorides giv

ChemInform Abstract: Highly Stereoselect
โœ T. YAMAZAKI; H. UMETANI; T. KITAZUME ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 32 KB ๐Ÿ‘ 2 views

Highly Stereoselective SN2' Reactions of Grignard Reagents Towards CF3-Containing Allylic Acetates. -The ฮณ-trifluoromethylated allylic acetates react with Grignard reagents in the presence of catalytic CuCN/TmsCl to form the products ( III) and (IV) resulting exclusively from an SN2' type reaction.