Issue 5, 1991

A singular substituent effect in the nickel(0) mediated cocyclisation of octa-1,7-diynes with alkynols. One-step synthesis of tetralin lactones from acyclic precursors

Abstract

Whereas the reaction of simple octa-1,7-diynes is fruitless, those bearing ester groups on the terminal positions react with alkynols in the presence of stoichiometric amounts of a nickel(0) reagent derived from NiCl2(PPh3)2 and BunLi to give tetralin lactones in moderate to good yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 277-278

A singular substituent effect in the nickel(0) mediated cocyclisation of octa-1,7-diynes with alkynols. One-step synthesis of tetralin lactones from acyclic precursors

P. Bhatarah and E. H. Smith, J. Chem. Soc., Chem. Commun., 1991, 277 DOI: 10.1039/C39910000277

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