Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 22nd May 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 7, 2019
Previous Article Next Article

Palladium-catalyzed intramolecular carboborylation of 1,3-diene and synthesis of ABCD ring of communesins

Author affiliations

Abstract

A palladium-catalyzed intramolecular carboborylation of 1,3-diene has been developed for the synthesis of iminoindolines with a quaternary carbon centre. This method was applied to a substrate bearing several functional groups to afford a complex iminoindoline, which was subsequently converted into an ABCD ring model compound of communesins via an intramolecular Friedel–Crafts-type reaction.

Graphical abstract: Palladium-catalyzed intramolecular carboborylation of 1,3-diene and synthesis of ABCD ring of communesins

Back to tab navigation

Supplementary files

Publication details

The article was received on 09 Sep 2018, accepted on 03 Oct 2018 and first published on 04 Oct 2018


Article type: Communication
DOI: 10.1039/C8OB02224K
Org. Biomol. Chem., 2019,17, 1731-1735

  •   Request permissions

    Palladium-catalyzed intramolecular carboborylation of 1,3-diene and synthesis of ABCD ring of communesins

    C. Tsukano, M. Nakajima, S. M. Hande and Y. Takemoto, Org. Biomol. Chem., 2019, 17, 1731
    DOI: 10.1039/C8OB02224K

Search articles by author

Spotlight

Advertisements