Issue 35, 2020

One-step synthesis of benzo[b]thiophenes by aryne reaction with alkynyl sulfides

Abstract

An aryne reaction with alkynyl sulfides affording benzo[b]thiophenes is disclosed. A wide range of 3-substituted benzothiophenes were synthesized from easily available o-silylaryl triflates and alkynyl sulfides in a one-step intermolecular manner. The synthesis of diverse multisubstituted benzothiophene derivatives involving a pentacyclic compound was achieved by virtue of the good functional group tolerance and versatile C2 functionalizations.

Graphical abstract: One-step synthesis of benzo[b]thiophenes by aryne reaction with alkynyl sulfides

Supplementary files

Article information

Article type
Edge Article
Submitted
13 Aug 2020
Accepted
26 Aug 2020
First published
01 Sep 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2020,11, 9691-9696

One-step synthesis of benzo[b]thiophenes by aryne reaction with alkynyl sulfides

T. Matsuzawa, T. Hosoya and S. Yoshida, Chem. Sci., 2020, 11, 9691 DOI: 10.1039/D0SC04450D

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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