Reactions with aziridines. 33. Arene hydrides. Part 1. Highly regioselective ring cleavage of N-acylaziridines by "anthracene hydride" (anion of 9,10-dihydroanthracene). Intermediacy of a carbonyl adduct. Influence of nitrogen inversion on the ring opening
Single-electrontransferreactions between tritylanion and 1-acyl-2,2-dimethylaziridines provide, among other products, the methallyl amides 7 and the triphenylmethanes 8 carrying an amidoethyl chain attached with the tertiary carbon ortho to the triphenylmethane.
STAMM, H.;SOMMER, A.;WODERER, A.;WIESERT, W.;MALL, T.;ASSITHIANAKIS, P., J. ORG. CHEM., 1985, 50, N 24, 4946-4955
作者:STAMM, H.、SOMMER, A.、WODERER, A.、WIESERT, W.、MALL, T.、ASSITHIANAKIS, P.
DOI:——
日期:——
Reactions with aziridines. 33. Arene hydrides. Part 1. Highly regioselective ring cleavage of N-acylaziridines by "anthracene hydride" (anion of 9,10-dihydroanthracene). Intermediacy of a carbonyl adduct. Influence of nitrogen inversion on the ring opening