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Modular Synthesis of Polycyclic Alkaloid Scaffolds via an Enantioselective Dearomative Cascade
[Image: see text] The polycyclic core of the akuammiline alkaloids can be synthesized from simple tryptamine and tryptophol derivatives via a Ag(I)-catalyzed enantioselective dearomative cyclization cascade sequence. The complex tetracyclic scaffolds are prepared via a rapid, versatile, three-step m...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145359/ https://www.ncbi.nlm.nih.gov/pubmed/31940208 http://dx.doi.org/10.1021/acs.orglett.0c00053 |
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author | Rossi-Ashton, James A. Clarke, Aimee K. Taylor, Richard J. K. Unsworth, William P. |
author_facet | Rossi-Ashton, James A. Clarke, Aimee K. Taylor, Richard J. K. Unsworth, William P. |
author_sort | Rossi-Ashton, James A. |
collection | PubMed |
description | [Image: see text] The polycyclic core of the akuammiline alkaloids can be synthesized from simple tryptamine and tryptophol derivatives via a Ag(I)-catalyzed enantioselective dearomative cyclization cascade sequence. The complex tetracyclic scaffolds are prepared via a rapid, versatile, three-step modular synthesis from simple commercially available indole derivatives in high yields and enantiomeric excess (up to 99% yield and >99% ee). |
format | Online Article Text |
id | pubmed-7145359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71453592020-04-10 Modular Synthesis of Polycyclic Alkaloid Scaffolds via an Enantioselective Dearomative Cascade Rossi-Ashton, James A. Clarke, Aimee K. Taylor, Richard J. K. Unsworth, William P. Org Lett [Image: see text] The polycyclic core of the akuammiline alkaloids can be synthesized from simple tryptamine and tryptophol derivatives via a Ag(I)-catalyzed enantioselective dearomative cyclization cascade sequence. The complex tetracyclic scaffolds are prepared via a rapid, versatile, three-step modular synthesis from simple commercially available indole derivatives in high yields and enantiomeric excess (up to 99% yield and >99% ee). American Chemical Society 2020-01-15 2020-02-07 /pmc/articles/PMC7145359/ /pubmed/31940208 http://dx.doi.org/10.1021/acs.orglett.0c00053 Text en Copyright © 2020 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 | Rossi-Ashton, James A. Clarke, Aimee K. Taylor, Richard J. K. Unsworth, William P. Modular Synthesis of Polycyclic Alkaloid Scaffolds via an Enantioselective Dearomative Cascade |
title | Modular Synthesis of Polycyclic Alkaloid Scaffolds
via an Enantioselective Dearomative Cascade |
title_full | Modular Synthesis of Polycyclic Alkaloid Scaffolds
via an Enantioselective Dearomative Cascade |
title_fullStr | Modular Synthesis of Polycyclic Alkaloid Scaffolds
via an Enantioselective Dearomative Cascade |
title_full_unstemmed | Modular Synthesis of Polycyclic Alkaloid Scaffolds
via an Enantioselective Dearomative Cascade |
title_short | Modular Synthesis of Polycyclic Alkaloid Scaffolds
via an Enantioselective Dearomative Cascade |
title_sort | modular synthesis of polycyclic alkaloid scaffolds
via an enantioselective dearomative cascade |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145359/ https://www.ncbi.nlm.nih.gov/pubmed/31940208 http://dx.doi.org/10.1021/acs.orglett.0c00053 |
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