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50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling

The Zweifel olefination is a powerful method for the stereoselective synthesis of alkenes. The reaction proceeds in the absence of a transition-metal catalyst, instead taking place by iodination of vinyl boronate complexes. Pioneering studies into this reaction were reported in 1967 and this short r...

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Autores principales: Armstrong, Roly J., Aggarwal, Varinder K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376632/
http://dx.doi.org/10.1055/s-0036-1589046
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author Armstrong, Roly J.
Aggarwal, Varinder K.
author_facet Armstrong, Roly J.
Aggarwal, Varinder K.
author_sort Armstrong, Roly J.
collection PubMed
description The Zweifel olefination is a powerful method for the stereoselective synthesis of alkenes. The reaction proceeds in the absence of a transition-metal catalyst, instead taking place by iodination of vinyl boronate complexes. Pioneering studies into this reaction were reported in 1967 and this short review summarizes developments in the field over the past 50 years. An account of how the Zweifel olefination was modified to enable the coupling of robust and air-stable boronic esters is presented followed by a summary of current state of the art developments in the field, including stereodivergent olefination and alkynylation. Finally, selected applications of the Zweifel olefination in target-oriented synthesis are reviewed. 1 Introduction 2.1 Zweifel Olefination of Vinyl Boranes 2.2 Zweifel Olefination of Vinyl Borinic Esters 2.3 Extension to Boronic Esters 3.1 Introduction of an Unsubstituted Vinyl Group 3.2 Coupling of α-Substituted Vinyl Partners 3.3 Syn Elimination 4 Zweifel Olefination in Natural Product Synthesis 5 Conclusions and Outlook
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spelling pubmed-63766322019-02-19 50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling Armstrong, Roly J. Aggarwal, Varinder K. Synthesis (Stuttg) The Zweifel olefination is a powerful method for the stereoselective synthesis of alkenes. The reaction proceeds in the absence of a transition-metal catalyst, instead taking place by iodination of vinyl boronate complexes. Pioneering studies into this reaction were reported in 1967 and this short review summarizes developments in the field over the past 50 years. An account of how the Zweifel olefination was modified to enable the coupling of robust and air-stable boronic esters is presented followed by a summary of current state of the art developments in the field, including stereodivergent olefination and alkynylation. Finally, selected applications of the Zweifel olefination in target-oriented synthesis are reviewed. 1 Introduction 2.1 Zweifel Olefination of Vinyl Boranes 2.2 Zweifel Olefination of Vinyl Borinic Esters 2.3 Extension to Boronic Esters 3.1 Introduction of an Unsubstituted Vinyl Group 3.2 Coupling of α-Substituted Vinyl Partners 3.3 Syn Elimination 4 Zweifel Olefination in Natural Product Synthesis 5 Conclusions and Outlook Georg Thieme Verlag 2017-08-01 2017-07-11 /pmc/articles/PMC6376632/ http://dx.doi.org/10.1055/s-0036-1589046 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Armstrong, Roly J.
Aggarwal, Varinder K.
50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling
title 50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling
title_full 50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling
title_fullStr 50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling
title_full_unstemmed 50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling
title_short 50 Years of Zweifel Olefination: A Transition-Metal-Free Coupling
title_sort 50 years of zweifel olefination: a transition-metal-free coupling
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376632/
http://dx.doi.org/10.1055/s-0036-1589046
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