Atroposelective Synthesis of Axially Chiral Naphthylpyrroles by a Catalytic Asymmetric 1,3-Dipolar Cycloaddition/Aromatization Sequence-Reference-Cited by-同舟云学术

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Atroposelective Synthesis of Axially Chiral Naphthylpyrroles by a Catalytic Asymmetric 1,3-Dipolar Cycloaddition/Aromatization Sequence

Published:2024-01-24 Issue:4 Volume:26 Page:922-927
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Maclean Ian¹,Gallent Enrique¹,Orozco Oscar¹,Molina Alba¹,Rodríguez Nuria¹²^ORCID,Adrio Javier¹²^ORCID,Carretero Juan C.¹²^ORCID

Affiliation:

1. Departamento de Química Orgánica, Facultad de Ciencias, Universidad Autónoma de Madrid, 28049 Madrid, Spain

2. Institute for Advanced Research in Chemical Sciences (IAdChem) and Center for Innovation in Advanced Chemistry (ORFEO-CINQA), Universidad Autónoma de Madrid, 28049 Madrid, Spain

Funder

Ministerio de Ciencia, Innovaci?n y Universidades

European Regional Development Fund

Ministerio de Econom?a y Competitividad

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c04261

Reference29 articles.

1. Atropisomerism in medicinal chemistry: challenges and opportunities

2. Recent Advances in Catalytic Asymmetric Construction of Atropisomers

3. Atroposelective transformation of axially chiral (hetero)biaryls. From desymmetrization to modern resolution strategies

4. Synthesis of binaphthyl based phosphine and phosphite ligands

5. Enantioselective syntheses of atropisomers featuring a five-membered ring

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