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Asymmetric Synthesis of Nortropanes via Rh-Catalyzed Allylic Arylation
[Image: see text] Tropane derivatives are extensively used in medicine, but catalytic asymmetric methods for their synthesis are underexplored. Here, we report Rh-catalyzed asymmetric Suzuki–Miyaura-type cross-coupling reactions between a racemic N-Boc-nortropane-derived allylic chloride and (hetero...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361292/ https://www.ncbi.nlm.nih.gov/pubmed/35966601 http://dx.doi.org/10.1021/acscatal.2c02259 |
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author | Zhang, Yan Goetzke, F. Wieland Christensen, Kirsten E. Fletcher, Stephen P. |
author_facet | Zhang, Yan Goetzke, F. Wieland Christensen, Kirsten E. Fletcher, Stephen P. |
author_sort | Zhang, Yan |
collection | PubMed |
description | [Image: see text] Tropane derivatives are extensively used in medicine, but catalytic asymmetric methods for their synthesis are underexplored. Here, we report Rh-catalyzed asymmetric Suzuki–Miyaura-type cross-coupling reactions between a racemic N-Boc-nortropane-derived allylic chloride and (hetero)aryl boronic esters. The reaction proceeds via an unexpected kinetic resolution, and the resolved enantiopure allyl chloride can undergo highly enantiospecific reactions with N-, O-, and S-containing nucleophiles. The method was applied in a highly stereoselective formal synthesis of YZJ-1139(1), a potential insomnia treatment that recently completed Phase II clinical trials. Our report represents an asymmetric catalytic method for the synthesis of YZJ-1139(1) and related compounds. |
format | Online Article Text |
id | pubmed-9361292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-93612922022-08-10 Asymmetric Synthesis of Nortropanes via Rh-Catalyzed Allylic Arylation Zhang, Yan Goetzke, F. Wieland Christensen, Kirsten E. Fletcher, Stephen P. ACS Catal [Image: see text] Tropane derivatives are extensively used in medicine, but catalytic asymmetric methods for their synthesis are underexplored. Here, we report Rh-catalyzed asymmetric Suzuki–Miyaura-type cross-coupling reactions between a racemic N-Boc-nortropane-derived allylic chloride and (hetero)aryl boronic esters. The reaction proceeds via an unexpected kinetic resolution, and the resolved enantiopure allyl chloride can undergo highly enantiospecific reactions with N-, O-, and S-containing nucleophiles. The method was applied in a highly stereoselective formal synthesis of YZJ-1139(1), a potential insomnia treatment that recently completed Phase II clinical trials. Our report represents an asymmetric catalytic method for the synthesis of YZJ-1139(1) and related compounds. American Chemical Society 2022-07-12 2022-08-05 /pmc/articles/PMC9361292/ /pubmed/35966601 http://dx.doi.org/10.1021/acscatal.2c02259 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Zhang, Yan Goetzke, F. Wieland Christensen, Kirsten E. Fletcher, Stephen P. Asymmetric Synthesis of Nortropanes via Rh-Catalyzed Allylic Arylation |
title | Asymmetric Synthesis
of Nortropanes via Rh-Catalyzed Allylic Arylation |
title_full | Asymmetric Synthesis
of Nortropanes via Rh-Catalyzed Allylic Arylation |
title_fullStr | Asymmetric Synthesis
of Nortropanes via Rh-Catalyzed Allylic Arylation |
title_full_unstemmed | Asymmetric Synthesis
of Nortropanes via Rh-Catalyzed Allylic Arylation |
title_short | Asymmetric Synthesis
of Nortropanes via Rh-Catalyzed Allylic Arylation |
title_sort | asymmetric synthesis
of nortropanes via rh-catalyzed allylic arylation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9361292/ https://www.ncbi.nlm.nih.gov/pubmed/35966601 http://dx.doi.org/10.1021/acscatal.2c02259 |
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