Substitution of P(O)Ph2, SOPh and SO2Ph on an allene facilitates intramolecular radical addition to the central allene carbon to provide good yields of five-, six-, and seven-membered carbocycles.
Substitution of P(O)Ph2, SOPh and SO2Ph on an allene facilitates intramolecular radical addition to the central allene carbon to provide good yields of five-, six-, and seven-membered carbocycles.
HANNABY, MALCOLM;WARREN, STUART, J. CHEM. SOC. PERKIN TRANS. PT 1,(1989) N, C. 303-311
作者:HANNABY, MALCOLM、WARREN, STUART
DOI:——
日期:——
HANNABY, M.;WARREN, S., TETRAHEDRON LETT., 1985, 26, N 26, 3133-3136
作者:HANNABY, M.、WARREN, S.
DOI:——
日期:——
Radical cyclizations of functionalized allenes
作者:Jack K. Crandall、Timothy A. Ayers
DOI:10.1016/s0040-4039(00)79759-0
日期:1991.7
Substitution of P(O)Ph2, SOPh and SO2Ph on an allene facilitates intramolecular radical addition to the central allene carbon to provide good yields of five-, six-, and seven-membered carbocycles.