RADICAL CYCLIZATION OF N-AZIRIDINYLIMINES: ITS APPLICATION TO SESQUITERPENE
SYNTHESES VIA CONSECUTIVE CARBON-CARBON BOND FORMATION Page 161 RADICAL …

The conventional tandem cyclization reactions involve the formation of alternating carbon‐
carbon bonds, whereas the newly developed cyclization reactions involve the formation of …

The radical cyclizations using N-aziridinylimines for the formation of five-and six-membered
ring radicals from acyclic precursors are different from ordinary radical cyclizations using …

Despite the synthetic usefulness of radical cyclization reactions, 1 the cyclization pathway is
mainly limited to 5-exo closure along with somewhat less efficient 6-exo and 6-endo closure …

Further Studies on Radical Cyclizations of N-Aziridinyl Imines. Carhonyl and Alkenyl Group
vs. N-Aziridinyl Imino Group Competit Page 1 Temhcdron Letters. Vol. 34. No. 26, PP. 4213-4214.1993 …

N-Aziridinylimines have found many useful applications in organic synthesis due to their
ability to generate a variety of reactive intermediates such as cations, diazoalkanes and …

A fundamentally new approach, using 2-phenyl-N-aziridinyl imines, for the formation of five-
and six-membered ring radicals from acyclic precursors has been studied. The radical …

Radical cyclization of N-aziridinylimines provides a ready access to 5-and 6-membered ring
radicals, in which N-aziridinylimines are used as geminal radical acceptor and donor …

Substituent Control over the Regiochemistry of Ring Opening of 2-Aziridinylmethyl Radicals
Page 1 Tcmhcdmn Lctms. Vol. 34. No. 31. pp. 49014904.1993 Printed in Great Britain …

Regiospecific Radical-induced Cleavage of Aziridines: Syntheses of Allylic Amines and Pyrrol
id ines Page 1 434 J. CHEM. SOC., CHEM. COMMUN., 1990 Regiospecific Radical-induced …