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

Jerry Yang; Richard Weinberg; Ronald Breslow

doi:10.1039/b000463o

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

Jerry Yang, Richard Weinberg, Ronald Breslow^*

^*Corresponding author for this work

Medicine, Cardiology Division

Research output: Contribution to journal › Article › peer-review

98 Scopus citations

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.

Original language	English (US)
Pages (from-to)	531-532
Number of pages	2
Journal	Chemical Communications
Issue number	7
DOIs	https://doi.org/10.1039/b000463o
State	Published - Apr 7 2000

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
Chemistry(all)
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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

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.",

author = "Jerry Yang and Richard Weinberg and Ronald Breslow",

note = "Funding Information: The authors acknowledge funding from the National Institute of Minority Health and Health Disparities (MD 006923), the National Institute of Mental Health (MH 115344), the National Science Foundation Graduate Research Fellowship Program under grant no. DGE-1650604, and the UCLA Bedari Kindness Institute. J. G. Foster is supported by an Infosys Membership in the School of Social Science at the Institute for Advanced Study.",

year = "2000",

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doi = "10.1039/b000463o",

language = "English (US)",

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T1 - The hydroxylation and amidation of equilenin acetate catalyzed by chloro[5,10,15,20-tetrakis(pentafluorophenyl)porphyrinato]manganese(III)

AU - Yang, Jerry

AU - Weinberg, Richard

AU - Breslow, Ronald

N1 - Funding Information: The authors acknowledge funding from the National Institute of Minority Health and Health Disparities (MD 006923), the National Institute of Mental Health (MH 115344), the National Science Foundation Graduate Research Fellowship Program under grant no. DGE-1650604, and the UCLA Bedari Kindness Institute. J. G. Foster is supported by an Infosys Membership in the School of Social Science at the Institute for Advanced Study.

PY - 2000/4/7

Y1 - 2000/4/7

N2 - 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.

AB - 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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JO - Chemical Communications

JF - Chemical Communications

IS - 7

ER -

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

Abstract

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