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Programmed serial stereochemical relay and its application in the synthesis of morphinans

Herein we report a rationally designed, serial point-to-axial and axial-to-point stereoinduction and its integration into multi-step and target-oriented organic synthesis. In this proof-of-concept study, the configurational stability of several carefully designed atropisomeric intermediates and the...

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Detalles Bibliográficos
Autores principales: Ho (Kenny) Park, Kun, Chen, Rui, Chen, David Y.-K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642196/
https://www.ncbi.nlm.nih.gov/pubmed/29147530
http://dx.doi.org/10.1039/c7sc03189k
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author Ho (Kenny) Park, Kun
Chen, Rui
Chen, David Y.-K.
author_facet Ho (Kenny) Park, Kun
Chen, Rui
Chen, David Y.-K.
author_sort Ho (Kenny) Park, Kun
collection PubMed
description Herein we report a rationally designed, serial point-to-axial and axial-to-point stereoinduction and its integration into multi-step and target-oriented organic synthesis. In this proof-of-concept study, the configurational stability of several carefully designed atropisomeric intermediates and the fidelity of their unconventional stereoinductions were systematically investigated. The highly functionalized prepared synthetic intermediate was further applied in a novel chemical method to access the morphinans and it is potentially applicable to other structurally related alkaloids.
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spelling pubmed-56421962017-11-16 Programmed serial stereochemical relay and its application in the synthesis of morphinans Ho (Kenny) Park, Kun Chen, Rui Chen, David Y.-K. Chem Sci Chemistry Herein we report a rationally designed, serial point-to-axial and axial-to-point stereoinduction and its integration into multi-step and target-oriented organic synthesis. In this proof-of-concept study, the configurational stability of several carefully designed atropisomeric intermediates and the fidelity of their unconventional stereoinductions were systematically investigated. The highly functionalized prepared synthetic intermediate was further applied in a novel chemical method to access the morphinans and it is potentially applicable to other structurally related alkaloids. Royal Society of Chemistry 2017-10-01 2017-08-30 /pmc/articles/PMC5642196/ /pubmed/29147530 http://dx.doi.org/10.1039/c7sc03189k Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Ho (Kenny) Park, Kun
Chen, Rui
Chen, David Y.-K.
Programmed serial stereochemical relay and its application in the synthesis of morphinans
title Programmed serial stereochemical relay and its application in the synthesis of morphinans
title_full Programmed serial stereochemical relay and its application in the synthesis of morphinans
title_fullStr Programmed serial stereochemical relay and its application in the synthesis of morphinans
title_full_unstemmed Programmed serial stereochemical relay and its application in the synthesis of morphinans
title_short Programmed serial stereochemical relay and its application in the synthesis of morphinans
title_sort programmed serial stereochemical relay and its application in the synthesis of morphinans
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642196/
https://www.ncbi.nlm.nih.gov/pubmed/29147530
http://dx.doi.org/10.1039/c7sc03189k
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