Issue 0, 1982
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Convenient syntheses of 5-substituted 2- hydroxybenzoates and related reactions

Derek H. R. Barton,   Gilles Dressaire,   Brian J. Willis,   Anthony G. M. Barrett  and  Marc Pfeffer  

Abstract

The enamine aidehydes RC([double bond, length half m-dash]CHNMe2)CHO (R = Et or Ph) were condensed with the bis-enolate CH2[double bond, length half m-dash]C(O–)CH[double bond, length half m-dash]C(O–)OEt to give the title aromatic compounds. Thus these products are available from the acetals R1CH2CH(OR2)2(R1= R2= Et; R1= Ph, R2= Me) in two steps. The Vilsmeier formylation of several derivatives of butanal was examined.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/P19820000665
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1982, 665-669

Permissions

Request permissions

Convenient syntheses of 5-substituted 2- hydroxybenzoates and related reactions

D. H. R. Barton, G. Dressaire, B. J. Willis, A. G. M. Barrett and M. Pfeffer, J. Chem. Soc., Perkin Trans. 1, 1982, 665 DOI: 10.1039/P19820000665

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