How Do Analogous α-Chloroenamides and α-Iodoenamides Give Different Product Distributions in 5-Endo Radical Cyclizations?

DP Curran, DB Guthrie, SJ Geib

Index: Tamura, Osamu; Matsukida, Hana; Toyao, Atsushi; Takeda, Yoshifumi; Ishibashi, Hiroyuki Journal of Organic Chemistry, 2002 , vol. 67, # 16 p. 5537 - 5545

Full Text: HTML

Citation Number: 32

Abstract

... Journal of the ... Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260. J. Am. ... Along these lines, Ishibashi and co-workers postulated that chloride 1a might have a ground-state preference for E-amide rotamer 1aE (Figure 3), and thus its derived radical ...

Related Articles:

An Aza-Wittig/π-Furan Cyclization Approach Toward the Homoerythrina Alkaloid (±)-Selaginoidine

[Cassidy, Michael P.; Oezdemir, Ayse Daut; Padwa, Albert Organic Letters, 2005 , vol. 7, # 7 p. 1339 - 1342]

How Do Analogous α-Chloroenamides and α-Iodoenamides Give Different Product Distributions in 5-Endo Radical Cyclizations?

[Curran, Dennis P.; Guthrie, David B.; Geib, Steven J. Journal of the American Chemical Society, 2008 , vol. 130, # 26 p. 8437 - 8445]

More Articles...