Cargando…
Cobalt-catalyzed C(sp(3))–H/C(sp(2))–H oxidative coupling between alkanes and benzamides
A direct cobalt-catalyzed oxidative coupling between C(sp(2))–H in unactivated benzamides and C(sp(3))–H in simple alkanes, ethers and toluene derivatives was explored. This protocol achieves direct C–C formation without using alkyl or aryl halide surrogates and exhibits high practicality with ample...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079668/ https://www.ncbi.nlm.nih.gov/pubmed/35542514 http://dx.doi.org/10.1039/c8ra01377b |
_version_ | 1784702606979891200 |
---|---|
author | Li, Shuangjie Wang, Bao Dong, Guangyu Li, Chunpu Liu, Hong |
author_facet | Li, Shuangjie Wang, Bao Dong, Guangyu Li, Chunpu Liu, Hong |
author_sort | Li, Shuangjie |
collection | PubMed |
description | A direct cobalt-catalyzed oxidative coupling between C(sp(2))–H in unactivated benzamides and C(sp(3))–H in simple alkanes, ethers and toluene derivatives was explored. This protocol achieves direct C–C formation without using alkyl or aryl halide surrogates and exhibits high practicality with ample substrate scope. The method provides a new way to construct linear and five- or six-membered ring moieties in bioactive molecules. |
format | Online Article Text |
id | pubmed-9079668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90796682022-05-09 Cobalt-catalyzed C(sp(3))–H/C(sp(2))–H oxidative coupling between alkanes and benzamides Li, Shuangjie Wang, Bao Dong, Guangyu Li, Chunpu Liu, Hong RSC Adv Chemistry A direct cobalt-catalyzed oxidative coupling between C(sp(2))–H in unactivated benzamides and C(sp(3))–H in simple alkanes, ethers and toluene derivatives was explored. This protocol achieves direct C–C formation without using alkyl or aryl halide surrogates and exhibits high practicality with ample substrate scope. The method provides a new way to construct linear and five- or six-membered ring moieties in bioactive molecules. The Royal Society of Chemistry 2018-04-10 /pmc/articles/PMC9079668/ /pubmed/35542514 http://dx.doi.org/10.1039/c8ra01377b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Li, Shuangjie Wang, Bao Dong, Guangyu Li, Chunpu Liu, Hong Cobalt-catalyzed C(sp(3))–H/C(sp(2))–H oxidative coupling between alkanes and benzamides |
title | Cobalt-catalyzed C(sp(3))–H/C(sp(2))–H oxidative coupling between alkanes and benzamides |
title_full | Cobalt-catalyzed C(sp(3))–H/C(sp(2))–H oxidative coupling between alkanes and benzamides |
title_fullStr | Cobalt-catalyzed C(sp(3))–H/C(sp(2))–H oxidative coupling between alkanes and benzamides |
title_full_unstemmed | Cobalt-catalyzed C(sp(3))–H/C(sp(2))–H oxidative coupling between alkanes and benzamides |
title_short | Cobalt-catalyzed C(sp(3))–H/C(sp(2))–H oxidative coupling between alkanes and benzamides |
title_sort | cobalt-catalyzed c(sp(3))–h/c(sp(2))–h oxidative coupling between alkanes and benzamides |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079668/ https://www.ncbi.nlm.nih.gov/pubmed/35542514 http://dx.doi.org/10.1039/c8ra01377b |
work_keys_str_mv | AT lishuangjie cobaltcatalyzedcsp3hcsp2hoxidativecouplingbetweenalkanesandbenzamides AT wangbao cobaltcatalyzedcsp3hcsp2hoxidativecouplingbetweenalkanesandbenzamides AT dongguangyu cobaltcatalyzedcsp3hcsp2hoxidativecouplingbetweenalkanesandbenzamides AT lichunpu cobaltcatalyzedcsp3hcsp2hoxidativecouplingbetweenalkanesandbenzamides AT liuhong cobaltcatalyzedcsp3hcsp2hoxidativecouplingbetweenalkanesandbenzamides |