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Enantioselective Synthesis of 4- and 6-Azaindolines by a Cation-Directed Cyclization
[Image: see text] Functionalized 4- and 6-azaindolines are accessible with high levels of enantioselectivity by the cation-directed cyclization of aminopyridine-derived imines via phase-transfer catalysis. The extension of this methodology to diastereoselective cyclizations is also described.
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086784/ https://www.ncbi.nlm.nih.gov/pubmed/27709963 http://dx.doi.org/10.1021/acs.orglett.6b02744 |
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author | Lamb, Alan D. Davey, Peter D. Driver, Russell W. Thompson, Amber L. Smith, Martin D. |
author_facet | Lamb, Alan D. Davey, Peter D. Driver, Russell W. Thompson, Amber L. Smith, Martin D. |
author_sort | Lamb, Alan D. |
collection | PubMed |
description | [Image: see text] Functionalized 4- and 6-azaindolines are accessible with high levels of enantioselectivity by the cation-directed cyclization of aminopyridine-derived imines via phase-transfer catalysis. The extension of this methodology to diastereoselective cyclizations is also described. |
format | Online Article Text |
id | pubmed-5086784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50867842016-11-01 Enantioselective Synthesis of 4- and 6-Azaindolines by a Cation-Directed Cyclization Lamb, Alan D. Davey, Peter D. Driver, Russell W. Thompson, Amber L. Smith, Martin D. Org Lett [Image: see text] Functionalized 4- and 6-azaindolines are accessible with high levels of enantioselectivity by the cation-directed cyclization of aminopyridine-derived imines via phase-transfer catalysis. The extension of this methodology to diastereoselective cyclizations is also described. American Chemical Society 2016-10-06 2016-10-21 /pmc/articles/PMC5086784/ /pubmed/27709963 http://dx.doi.org/10.1021/acs.orglett.6b02744 Text en Copyright © 2016 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Lamb, Alan D. Davey, Peter D. Driver, Russell W. Thompson, Amber L. Smith, Martin D. Enantioselective Synthesis of 4- and 6-Azaindolines by a Cation-Directed Cyclization |
title | Enantioselective Synthesis of 4- and 6-Azaindolines
by a Cation-Directed Cyclization |
title_full | Enantioselective Synthesis of 4- and 6-Azaindolines
by a Cation-Directed Cyclization |
title_fullStr | Enantioselective Synthesis of 4- and 6-Azaindolines
by a Cation-Directed Cyclization |
title_full_unstemmed | Enantioselective Synthesis of 4- and 6-Azaindolines
by a Cation-Directed Cyclization |
title_short | Enantioselective Synthesis of 4- and 6-Azaindolines
by a Cation-Directed Cyclization |
title_sort | enantioselective synthesis of 4- and 6-azaindolines
by a cation-directed cyclization |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086784/ https://www.ncbi.nlm.nih.gov/pubmed/27709963 http://dx.doi.org/10.1021/acs.orglett.6b02744 |
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