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Catalytic Alkyne Allylboration: A Quest for Selectivity

[Image: see text] Catalytic methodologies that enable the synthesis of complex organic molecules from simple and readily available starting materials represent a goal in modern synthetic chemistry. In particular, multicomponent carboboration reactions that provide stereoselective access to densely f...

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Autores principales: Chaves-Pouso, Andrea, Rivera-Chao, Eva, Fañanás-Mastral, Martín
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563124/
https://www.ncbi.nlm.nih.gov/pubmed/37822858
http://dx.doi.org/10.1021/acscatal.3c03015
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author Chaves-Pouso, Andrea
Rivera-Chao, Eva
Fañanás-Mastral, Martín
author_facet Chaves-Pouso, Andrea
Rivera-Chao, Eva
Fañanás-Mastral, Martín
author_sort Chaves-Pouso, Andrea
collection PubMed
description [Image: see text] Catalytic methodologies that enable the synthesis of complex organic molecules from simple and readily available starting materials represent a goal in modern synthetic chemistry. In particular, multicomponent carboboration reactions that provide stereoselective access to densely functionalized building blocks are particularly valuable to achieve molecular diversity. This Perspective covers the developments in the area of catalytic allylboration of alkynes and highlights the key features that have allowed for the control of the regio-, diastereo-, and enantioselectivity in these transformations.
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spelling pubmed-105631242023-10-11 Catalytic Alkyne Allylboration: A Quest for Selectivity Chaves-Pouso, Andrea Rivera-Chao, Eva Fañanás-Mastral, Martín ACS Catal [Image: see text] Catalytic methodologies that enable the synthesis of complex organic molecules from simple and readily available starting materials represent a goal in modern synthetic chemistry. In particular, multicomponent carboboration reactions that provide stereoselective access to densely functionalized building blocks are particularly valuable to achieve molecular diversity. This Perspective covers the developments in the area of catalytic allylboration of alkynes and highlights the key features that have allowed for the control of the regio-, diastereo-, and enantioselectivity in these transformations. American Chemical Society 2023-09-13 /pmc/articles/PMC10563124/ /pubmed/37822858 http://dx.doi.org/10.1021/acscatal.3c03015 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Chaves-Pouso, Andrea
Rivera-Chao, Eva
Fañanás-Mastral, Martín
Catalytic Alkyne Allylboration: A Quest for Selectivity
title Catalytic Alkyne Allylboration: A Quest for Selectivity
title_full Catalytic Alkyne Allylboration: A Quest for Selectivity
title_fullStr Catalytic Alkyne Allylboration: A Quest for Selectivity
title_full_unstemmed Catalytic Alkyne Allylboration: A Quest for Selectivity
title_short Catalytic Alkyne Allylboration: A Quest for Selectivity
title_sort catalytic alkyne allylboration: a quest for selectivity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563124/
https://www.ncbi.nlm.nih.gov/pubmed/37822858
http://dx.doi.org/10.1021/acscatal.3c03015
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