Decarbonylative Radical Cyclization of α-Amino Selenoesters upon Electrophilic Alkenes. A General Method for the 6-Azabicyclo[3.2.1]octane Synthesis
2002; American Chemical Society; Volume: 67; Issue: 7 Linguagem: Inglês
10.1021/jo0163849
ISSN1520-6904
AutoresJosefina Quirante, Xavier Vilà, Carmen Escolano, Josep Bonjoch,
Tópico(s)Catalytic C–H Functionalization Methods
Resumoalpha-Amino selenoester-tethered electronically poor alkenes on treatment with tributyltin hydride or TTMSS undergo intramolecular radical cyclization to provide 6-azabicyclo[3.2.1]octanes through 1-aminomethyl radical intermediates.
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