6030-91-7Relevant articles and documents
The hydroxylation and amidation of equilenin acetate catalyzed by chloro[5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato]manganese(III)
Yang, Jerry,Weinberg, Richard,Breslow, Ronald
, p. 531 - 532 (2000)
The aromatic steroid equilenin acetate undergoes regioselective and stereoselective hydroxylation and amidation catalyzed by a manganese porphyrin using iodosobenzene (PhIO) and N-tosyliminophenyliodinane (PhINTs) as the oxygen and nitrogen donor, respectively.
An effective approach to B-ring aromatization of equilin
Cao, Zhisong,Liehr, Joachim G.
, p. 145 - 155 (2007/10/03)
Epoxidation of equilin followed by rearrangement-elimination catalyzed by either proton acids or Lewis acids generates an estrogen with an aromatic B-ring. This procedure represents an effective method for the conversion of an equilin nucleus to an equilenin nucleus.