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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...

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Autores principales: Rossi-Ashton, James A., Clarke, Aimee K., Taylor, Richard J. K., Unsworth, William P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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).
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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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