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Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli–Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides

A modular and functional group-tolerant protocol for the transition metal-free coupling of novel N,O- and N,S-heterocyclic vinyl chlorides with terminal acetylenes and styrenes has been developed, leading to the epimerization-free synthesis of fully carbofunctionalized dihydro-1,4-oxazines/thiazines...

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Detalles Bibliográficos
Autores principales: Beng, Timothy K., Farah, Abdikani Omar, Shearer, Victoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057152/
https://www.ncbi.nlm.nih.gov/pubmed/35521247
http://dx.doi.org/10.1039/d0ra06619b
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author Beng, Timothy K.
Farah, Abdikani Omar
Shearer, Victoria
author_facet Beng, Timothy K.
Farah, Abdikani Omar
Shearer, Victoria
author_sort Beng, Timothy K.
collection PubMed
description A modular and functional group-tolerant protocol for the transition metal-free coupling of novel N,O- and N,S-heterocyclic vinyl chlorides with terminal acetylenes and styrenes has been developed, leading to the epimerization-free synthesis of fully carbofunctionalized dihydro-1,4-oxazines/thiazines. Bicyclic morpholines have also been prepared through the interrogation of newly synthesized cross-conjugated dienes in Diels–Alder reactions. The use of environmentally benign reaction media endows the current strategy with a practical advantage.
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spelling pubmed-90571522022-05-04 Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli–Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides Beng, Timothy K. Farah, Abdikani Omar Shearer, Victoria RSC Adv Chemistry A modular and functional group-tolerant protocol for the transition metal-free coupling of novel N,O- and N,S-heterocyclic vinyl chlorides with terminal acetylenes and styrenes has been developed, leading to the epimerization-free synthesis of fully carbofunctionalized dihydro-1,4-oxazines/thiazines. Bicyclic morpholines have also been prepared through the interrogation of newly synthesized cross-conjugated dienes in Diels–Alder reactions. The use of environmentally benign reaction media endows the current strategy with a practical advantage. The Royal Society of Chemistry 2020-10-07 /pmc/articles/PMC9057152/ /pubmed/35521247 http://dx.doi.org/10.1039/d0ra06619b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Beng, Timothy K.
Farah, Abdikani Omar
Shearer, Victoria
Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli–Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides
title Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli–Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides
title_full Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli–Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides
title_fullStr Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli–Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides
title_full_unstemmed Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli–Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides
title_short Modular synthesis and transition metal-free alkynylation/alkenylation of Castagnoli–Cushman-derived N,O- and N,S-heterocyclic vinyl chlorides
title_sort modular synthesis and transition metal-free alkynylation/alkenylation of castagnoli–cushman-derived n,o- and n,s-heterocyclic vinyl chlorides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057152/
https://www.ncbi.nlm.nih.gov/pubmed/35521247
http://dx.doi.org/10.1039/d0ra06619b
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