Cargando…

Triphenylborane in Metal-Free Catalysis

The development and application of new organoboron reagents as Lewis acids in synthesis and metal-free catalysis have dramatically expanded over the past 20 years. In this context, we will show the recent uses of the simple and relatively weak Lewis acid BPh(3)—discovered 100 years ago—as a metal-fr...

Descripción completa

Detalles Bibliográficos
Autores principales: Mummadi, Suresh, Krempner, Clemens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9920172/
https://www.ncbi.nlm.nih.gov/pubmed/36771006
http://dx.doi.org/10.3390/molecules28031340
_version_ 1784887005134454784
author Mummadi, Suresh
Krempner, Clemens
author_facet Mummadi, Suresh
Krempner, Clemens
author_sort Mummadi, Suresh
collection PubMed
description The development and application of new organoboron reagents as Lewis acids in synthesis and metal-free catalysis have dramatically expanded over the past 20 years. In this context, we will show the recent uses of the simple and relatively weak Lewis acid BPh(3)—discovered 100 years ago—as a metal-free catalyst for various organic transformations. The first part will highlight catalytic applications in polymer synthesis such as the copolymerization of epoxides with CO(2), isocyanate, and organic anhydrides to various polycarbonate copolymers and controlled diblock copolymers as well as alternating polyurethanes. This is followed by a discussion of BPh(3) as a Lewis acid component in the frustrated Lewis pair (FLP) mediated cleavage of hydrogen and hydrogenation catalysis. In addition, BPh(3)-catalyzed reductive N-methylations and C-methylations with CO(2) and silane to value-added organic products will be covered as well along with BPh(3)-catalyzed cycloadditions and insertion reactions. Collectively, this mini-review showcases the underexplored potential of commercially available BPh(3) in metal-free catalysis.
format Online
Article
Text
id pubmed-9920172
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-99201722023-02-12 Triphenylborane in Metal-Free Catalysis Mummadi, Suresh Krempner, Clemens Molecules Review The development and application of new organoboron reagents as Lewis acids in synthesis and metal-free catalysis have dramatically expanded over the past 20 years. In this context, we will show the recent uses of the simple and relatively weak Lewis acid BPh(3)—discovered 100 years ago—as a metal-free catalyst for various organic transformations. The first part will highlight catalytic applications in polymer synthesis such as the copolymerization of epoxides with CO(2), isocyanate, and organic anhydrides to various polycarbonate copolymers and controlled diblock copolymers as well as alternating polyurethanes. This is followed by a discussion of BPh(3) as a Lewis acid component in the frustrated Lewis pair (FLP) mediated cleavage of hydrogen and hydrogenation catalysis. In addition, BPh(3)-catalyzed reductive N-methylations and C-methylations with CO(2) and silane to value-added organic products will be covered as well along with BPh(3)-catalyzed cycloadditions and insertion reactions. Collectively, this mini-review showcases the underexplored potential of commercially available BPh(3) in metal-free catalysis. MDPI 2023-01-31 /pmc/articles/PMC9920172/ /pubmed/36771006 http://dx.doi.org/10.3390/molecules28031340 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mummadi, Suresh
Krempner, Clemens
Triphenylborane in Metal-Free Catalysis
title Triphenylborane in Metal-Free Catalysis
title_full Triphenylborane in Metal-Free Catalysis
title_fullStr Triphenylborane in Metal-Free Catalysis
title_full_unstemmed Triphenylborane in Metal-Free Catalysis
title_short Triphenylborane in Metal-Free Catalysis
title_sort triphenylborane in metal-free catalysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9920172/
https://www.ncbi.nlm.nih.gov/pubmed/36771006
http://dx.doi.org/10.3390/molecules28031340
work_keys_str_mv AT mummadisuresh triphenylboraneinmetalfreecatalysis
AT krempnerclemens triphenylboraneinmetalfreecatalysis