Issue 41, 2017

Heteroannulation enabled by a bimetallic Rh(iii)/Ag(i) relay catalysis: application in the total synthesis of aristolactam BII

Abstract

A redox-neutral bimetallic Rh(III)/Ag(I) relay catalysis allowed the efficient construction of 3-alkylidene isoindolinones and 3-alkylidene isobenzofuranones. The Rh(III) catalyst was responsible for the C–H monofluoroalkenylation reaction, whereas the Ag(I) salt was an activator for the follow-up cyclization. The methodology developed was applied as a key step in the rapid total synthesis of the natural product aristolactam BII.

Graphical abstract: Heteroannulation enabled by a bimetallic Rh(iii)/Ag(i) relay catalysis: application in the total synthesis of aristolactam BII

Supplementary files

Article information

Article type
Communication
Submitted
20 Mar 2017
Accepted
02 May 2017
First published
02 May 2017

Chem. Commun., 2017,53, 5665-5668

Heteroannulation enabled by a bimetallic Rh(III)/Ag(I) relay catalysis: application in the total synthesis of aristolactam BII

W. Ji, E. Lin, Q. Li and H. Wang, Chem. Commun., 2017, 53, 5665 DOI: 10.1039/C7CC02105D

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