Issue 0, 1972
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Organolithium chemistry of N-heterocycles. Part IV. Formation of 1,2,4,5-tetrahydro-4,4-diphenyl-2,5-methano-3,1-benzoxazepines from quinolines

C. E. Crawforth,   O. Meth-Cohn  and  C. A. Russell  

Abstract

Certain quinolines react with the anion (Ph2COLi)– derived from benzophenone and excess of lithium to give high yields of 1,2,4,5-tetrahydro-4,4-diphenyl-2,5-methano-3,1 -benzoxazepines (I). These may be smoothly converted by 70% sulphuric acid into 4-(diphenylmethyl) quinolines (VIII).

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/P19720001176
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 1176-1179

Permissions

Request permissions

Organolithium chemistry of N-heterocycles. Part IV. Formation of 1,2,4,5-tetrahydro-4,4-diphenyl-2,5-methano-3,1-benzoxazepines from quinolines

C. E. Crawforth, O. Meth-Cohn and C. A. Russell, J. Chem. Soc., Perkin Trans. 1, 1972, 1176 DOI: 10.1039/P19720001176

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements