STUDIES IN THE WAGNER–MEERWEIN REARRANGEMENT: PART IV. DERIVATIVES OF BENZ[b]FLUORENE

Author:

Anet F. A. L.,Bavin P. M. G.

Abstract

10-Methyl-10-benz[b]fluorenylmethyl tosylate gave mainly 5-methylbenz[a]anthracene on formolysis, but the related alcohol gave a mixture of the 5- and 6-methyl isomers by reaction with phosphorus pentoxide. Reaction of benz[b]fluorenone with excess diazomethane gave 5-methoxybenz[a]anthracene as the only isolable product. The alkylation of methyl benz[b]fluorene-10-carboxylate was studied.

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Cited by 5 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. In Memoriam: The Life and Scientific Accomplishments of Frank A. L. Anet (1926–2024);Journal of Physical Organic Chemistry;2024-08-26

2. Wagner-Meerwein Rearrangement;Comprehensive Organic Name Reactions and Reagents;2010-09-15

3. SYNTHESIS OF SUBSTITUTED BENZ[A]ANTHRACENES;Journal of Synthetic Organic Chemistry, Japan;1978

4. The synthesis of phenanthrenes;Chemical Reviews;1976-10-01

5. 5,6-DIMETHYLBENZ[a]ANTHRACENE AND 5,6-DIMETHYLBENZO[c]PHENANTHRENE;Canadian Journal of Chemistry;1962-07-01

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