Issue 7, 2000
From the journal:

Chemical Communications

The hydroxylation and amidation of equilenin acetate catalyzed by chloro[5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato]manganese(iii)

Jerry Yang,a   Richard Weinberga  and  Ronald Breslow*a  

* Corresponding authors

a Department of Chemistry, Columbia University, New York, NY, USA.
E-mail: rb33@columbia.edu

Abstract

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.

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Article information

DOI
https://doi.org/10.1039/B000463O
Article type
Communication
Submitted
11 Jan 2000
Accepted
14 Feb 2000
First published
13 Mar 2000

Chem. Commun., 2000, 531-532

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The hydroxylation and amidation of equilenin acetate catalyzed by chloro[5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato]manganese(III)

J. Yang, R. Weinberg and R. Breslow, Chem. Commun., 2000, 531 DOI: 10.1039/B000463O

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