A Mechanistic Approach to the Reaction of 2,6-Di-tert-butylphenol with an Iodinating Agent in Methanol: Electrophilically Assisted Solvolysis of Intermediary 4-Iodocyclohexa-2,5-dienones-Reference-Cited by-同舟云学术

A Mechanistic Approach to the Reaction of 2,6-Di-tert-butylphenol with an Iodinating Agent in Methanol: Electrophilically Assisted Solvolysis of Intermediary 4-Iodocyclohexa-2,5-dienones

Published:1996-01-01 Issue:6 Volume:61 Page:2006-2012
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Omura Kanji¹

Affiliation:

1. College of Nutrition, Koshien University, Momijigaoka, Takarazuka, Hyogo 665, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo951455n

Reference23 articles.

1. The Iodination of Tyrosine and its Derivatives

2. One-Step Synthesis of Polyalkyl-2-iodo-p-benzoquinones

3. Lübbecke, H.; Boldt, P.Tetrahedron1978,34, 1557.

4. Facile and convenient syntheses of quinones from phenols

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