Model Reactions for the Biosynthesis of Thyroxine. XIX. The Formation of a Thyroxine Precursor by Photooxidation of 4-Hydroxy-3,5-diiodophenylpyruvic Acid in Organic Solvents-Reference-Cited by-同舟云学术

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Model Reactions for the Biosynthesis of Thyroxine. XIX. The Formation of a Thyroxine Precursor by Photooxidation of 4-Hydroxy-3,5-diiodophenylpyruvic Acid in Organic Solvents

Published:1972-09 Issue:9 Volume:45 Page:2866-2871
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Omura Kanji,Nishinaga Akira,Matsuura Teruo

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/45/9/45_9_2866/_pdf

Reference13 articles.

1. Reaction of 4-Hydroxy-3,5-diiodophenylpyruvic Acid with 3,5-Diiodotyrosine

2. Model reactions for the biosynthesis of thyroxine. XII. Nature of a thyroxine precursor formed in the synthesis of thyroxine from diiodotyrosine and its keto acid analog

3. Photosensitized oxygenation of 3-hydroxyflavones. Possible model for biological oxygenation

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A CONVENIENT PREPARATION OF DIPHENYLMETHANES FROM BROMOBENZENES USING THE GRIGNARD CROSS-COUPLING REACTION;Organic Preparations and Procedures International;1991-10

2. Bio-mimetic oxygenation;Tetrahedron;1977-01

3. ChemInform Abstract: MODELL-RK. FUER DIE BIOSYNTH. VON THYROXIN 19. MITT. PHOTOINDUZIERTE RK. 55. MITT. BLDG. EINES THYROXIN-VORLAEUFERS DURCH PHOTOOX. VON (4-HYDROXY-3,5-DIJOD-PHENYL)-BRENZTRAUBENSAEURE IN ORGANISCHEN LOESUNGSMITTELN;Chemischer Informationsdienst;1972-12-12

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