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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/16428
Title: Aminoselenenylation of alkenes: syntheses of β-phenylseleno carbamates and β-phenylseleno cyanamides
Authors: Francisco, Cosme G. ; Hernández, Rosendo ; León, Elisa I. ; Salazar, José A.; Suárez, Ernesto
Issue Date: 1990
Publisher: Royal Society of Chemistry (Great Britain)
Citation: Journal of the Chemical Society - Perkin Transactions 1990(9): 2417-2427 (1990)
Abstract: β-(Phenylseleno)alkylcarbamates and β-(phenylseleno)alkylcyanamides have been synthesized in good yields by reaction of alkenes with carbamates and cyanamide, respectively, in presence of benzeneselenenyl chloride–silver tetrafluoroborate or N-phenylselenophthalimide–H+. The subsequent reductive or oxidative removal of the phenylseleno group affords alkylcarbamates and alkylcyanamides, and allylic carbamates, cyanamides, and cyanimides.
Description: 11 pages, 4 tables, 6 schemes.
Publisher version (URL): http://dx.doi.org/10.1039/P19900002417
URI: http://hdl.handle.net/10261/16428
DOI: 10.1039/P19900002417
ISSN: 1472-7781
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