Cargando…

Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis

The synthesis and Cu/Pd-catalyzed arylboration of 1-silyl-1,3-cyclohexadiene is described. This diene is significant as it allows for synthesis of polyfunctional cyclohexane/enes. To achieve high levels of diastereoselectivity, the use of a pyridylidene Cu-complex was employed. In addition, through...

Descripción completa

Detalles Bibliográficos
Autores principales: Crook, Phillip F., Lear, Alan R., Das, Suman, Brown, M. Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548526/
https://www.ncbi.nlm.nih.gov/pubmed/37799986
http://dx.doi.org/10.1039/d3sc02536e
_version_ 1785115285947154432
author Crook, Phillip F.
Lear, Alan R.
Das, Suman
Brown, M. Kevin
author_facet Crook, Phillip F.
Lear, Alan R.
Das, Suman
Brown, M. Kevin
author_sort Crook, Phillip F.
collection PubMed
description The synthesis and Cu/Pd-catalyzed arylboration of 1-silyl-1,3-cyclohexadiene is described. This diene is significant as it allows for synthesis of polyfunctional cyclohexane/enes. To achieve high levels of diastereoselectivity, the use of a pyridylidene Cu-complex was employed. In addition, through the use of a chiral catalyst, an enantioselective reaction was possible. Due to the presence of the silyl and boron substituents, the products can be easily diversified into a range of valuable cyclohexane/ene products.
format Online
Article
Text
id pubmed-10548526
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-105485262023-10-05 Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis Crook, Phillip F. Lear, Alan R. Das, Suman Brown, M. Kevin Chem Sci Chemistry The synthesis and Cu/Pd-catalyzed arylboration of 1-silyl-1,3-cyclohexadiene is described. This diene is significant as it allows for synthesis of polyfunctional cyclohexane/enes. To achieve high levels of diastereoselectivity, the use of a pyridylidene Cu-complex was employed. In addition, through the use of a chiral catalyst, an enantioselective reaction was possible. Due to the presence of the silyl and boron substituents, the products can be easily diversified into a range of valuable cyclohexane/ene products. The Royal Society of Chemistry 2023-09-13 /pmc/articles/PMC10548526/ /pubmed/37799986 http://dx.doi.org/10.1039/d3sc02536e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Crook, Phillip F.
Lear, Alan R.
Das, Suman
Brown, M. Kevin
Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis
title Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis
title_full Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis
title_fullStr Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis
title_full_unstemmed Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis
title_short Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis
title_sort cu/pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10548526/
https://www.ncbi.nlm.nih.gov/pubmed/37799986
http://dx.doi.org/10.1039/d3sc02536e
work_keys_str_mv AT crookphillipf cupdcatalyzedarylborationofa1silyl13cyclohexadieneforstereocontrolledanddiversecyclohexaneenesynthesis
AT learalanr cupdcatalyzedarylborationofa1silyl13cyclohexadieneforstereocontrolledanddiversecyclohexaneenesynthesis
AT dassuman cupdcatalyzedarylborationofa1silyl13cyclohexadieneforstereocontrolledanddiversecyclohexaneenesynthesis
AT brownmkevin cupdcatalyzedarylborationofa1silyl13cyclohexadieneforstereocontrolledanddiversecyclohexaneenesynthesis