Model Reactions of Thyroxine Biosynthesis. Identification of the Key Intermediates in Thyroxine Formation from 3,5-Diiodo-l-tyrosine and 4-Hydroxy-3,5-diiodophenylpyruvic Acid-Reference-Cited by-同舟云学术

Model Reactions of Thyroxine Biosynthesis. Identification of the Key Intermediates in Thyroxine Formation from 3,5-Diiodo-l-tyrosine and 4-Hydroxy-3,5-diiodophenylpyruvic Acid

Published:1997-11-01 Issue:46 Volume:119 Page:11315-11316
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Oza Vibha B.¹,Salamonczyk Grzegorz M.¹,Guo Zhi-wei¹,Sih Charles J.¹

Affiliation:

1. School of Pharmacy, University of Wisconsin 425 North Charter Street, Madison, Wisconsin 53706-1515

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9719034

Reference21 articles.

1. Evidence for a Radical Mechanism in Peroxidase-Catalyzed Coupling. I. Steady-State Experiments with Various Peroxidases

2. Formation of dehydroalanine residues during thyroid hormone synthesis in thyroglobulin.

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