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Electro-Olefination-A Catalyst Free Stereoconvergent Strategy for the Functionalization of Alkenes.

Authors :
Baumann AN
Music A
Dechent J
Müller N
Jagau TC
Didier D
Source :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2020 Jul 08; Vol. 26 (38), pp. 8382-8387. Date of Electronic Publication: 2020 Jun 25.
Publication Year :
2020

Abstract

Conventional methods carrying out C(sp <superscript>2</superscript> )-C(sp <superscript>2</superscript> ) bond formations are typically mediated by transition-metal-based catalysts. Herein, we conceptualize a complementary avenue to access such bonds by exploiting the potential of electrochemistry in combination with organoboron chemistry. We demonstrate a transition metal catalyst-free electrocoupling between (hetero)aryls and alkenes through readily available alkenyl-tri(hetero)aryl borate salts (ATBs) in a stereoconvergent fashion. This unprecedented transformation was investigated theoretically and experimentally and led to a library of functionalized alkenes. The concept was then carried further and applied to the synthesis of the natural product pinosylvin and the derivatization of the steroidal dehydroepiandrosterone (DHEA) scaffold.<br /> (© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.)

Details

Language :
English
ISSN :
1521-3765
Volume :
26
Issue :
38
Database :
MEDLINE
Journal :
Chemistry (Weinheim an der Bergstrasse, Germany)
Publication Type :
Academic Journal
Accession number :
32203624
Full Text :
https://doi.org/10.1002/chem.202001394