Journal of the Chemical Society. Chemical communications p. 1671 (1986)
Update date:2022-08-03
Topics: Characterization Iodine-induced cyclization Regio-selective Chemo-selective Sulphur-carbon bond formation Spectral data Thioamide Carbon-heteroatom bond Synthon Solvent Ring closure Workup and Isolation Reaction Conditions γ,δ-Unsaturated Secondary Thioamides Iodoiminothiolactonization Reagent Formation of Iodoiminothiolactone Intermediate Amino Group Introduction
Takahata, Hiroki
Moriyama, Keiko
Moruyama, Mihoko
Yamazaki, Takao
Iodine-induced cyclization of γ,δ-unsaturated secondary thioamides proceeds regio- and chemo-selectively, providing, after elaboration, 2-aminothiophenes.
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Doi:10.1016/S0008-6215(00)90119-8
(1986)Doi:10.1016/S0040-4039(00)02288-7
(2001)Doi:10.1002/ejoc.201200081
(2012)Doi:10.3184/030823407X255533
(2007)Doi:10.1002/hlca.19860690822
(1986)Doi:10.1039/P19870000251
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