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Divergent C—H Insertion–Cyclization Cascades of N‐Allyl Ynamides
Gold carbene reactivity patterns were accessed by ynamide insertion into a C(sp(3))—H bond. A substantial increase in molecular complexity occurred through the cascade polycyclization of N‐allyl ynamides to form fused nitrogen‐heterocycle scaffolds. Exquisite selectivity was observed despite several...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY‐VCH Verlag
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832826/ https://www.ncbi.nlm.nih.gov/pubmed/26515958 http://dx.doi.org/10.1002/anie.201507167 |
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author | Adcock, Holly V. Chatzopoulou, Elli Davies, Paul W. |
author_facet | Adcock, Holly V. Chatzopoulou, Elli Davies, Paul W. |
author_sort | Adcock, Holly V. |
collection | PubMed |
description | Gold carbene reactivity patterns were accessed by ynamide insertion into a C(sp(3))—H bond. A substantial increase in molecular complexity occurred through the cascade polycyclization of N‐allyl ynamides to form fused nitrogen‐heterocycle scaffolds. Exquisite selectivity was observed despite several competing pathways in an efficient gold‐catalyzed synthesis of densely functionalized C(sp(3))‐rich polycycles and a copper‐catalyzed synthesis of fused pyridine derivatives. The respective gold–keteniminium and ketenimine activation pathways have been explored through a structure–reactivity study, and isotopic labeling identified turnover‐limiting C—H bond‐cleavage in both processes. |
format | Online Article Text |
id | pubmed-4832826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | WILEY‐VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-48328262016-04-27 Divergent C—H Insertion–Cyclization Cascades of N‐Allyl Ynamides Adcock, Holly V. Chatzopoulou, Elli Davies, Paul W. Angew Chem Int Ed Engl Communications Gold carbene reactivity patterns were accessed by ynamide insertion into a C(sp(3))—H bond. A substantial increase in molecular complexity occurred through the cascade polycyclization of N‐allyl ynamides to form fused nitrogen‐heterocycle scaffolds. Exquisite selectivity was observed despite several competing pathways in an efficient gold‐catalyzed synthesis of densely functionalized C(sp(3))‐rich polycycles and a copper‐catalyzed synthesis of fused pyridine derivatives. The respective gold–keteniminium and ketenimine activation pathways have been explored through a structure–reactivity study, and isotopic labeling identified turnover‐limiting C—H bond‐cleavage in both processes. WILEY‐VCH Verlag 2015-10-30 2015-12-14 /pmc/articles/PMC4832826/ /pubmed/26515958 http://dx.doi.org/10.1002/anie.201507167 Text en © 2015 The Authors. Published by Wiley‐VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. Open access. |
spellingShingle | Communications Adcock, Holly V. Chatzopoulou, Elli Davies, Paul W. Divergent C—H Insertion–Cyclization Cascades of N‐Allyl Ynamides |
title | Divergent C—H Insertion–Cyclization Cascades of N‐Allyl Ynamides |
title_full | Divergent C—H Insertion–Cyclization Cascades of N‐Allyl Ynamides |
title_fullStr | Divergent C—H Insertion–Cyclization Cascades of N‐Allyl Ynamides |
title_full_unstemmed | Divergent C—H Insertion–Cyclization Cascades of N‐Allyl Ynamides |
title_short | Divergent C—H Insertion–Cyclization Cascades of N‐Allyl Ynamides |
title_sort | divergent c—h insertion–cyclization cascades of n‐allyl ynamides |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832826/ https://www.ncbi.nlm.nih.gov/pubmed/26515958 http://dx.doi.org/10.1002/anie.201507167 |
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