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
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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 ...
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