β-Cyclodextrin–NHC–Au(I)-Catalyzed Enantioconvergent 1,5-Enyne Cycloisomerizations-Reference-Cited by-同舟云学术

β-Cyclodextrin–NHC–Au(I)-Catalyzed Enantioconvergent 1,5-Enyne Cycloisomerizations

Published:2024-07-01 Issue:27 Volume:26 Page:5817-5821
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Koohgard Mehdi¹,Enders Lukas¹²^ORCID,del Rio Natalia¹,Li Hang¹,Moccia Fabio¹,Khaled Omar¹,Bistri Olivia¹,Helaja Juho²^ORCID,Sollogoub Matthieu¹^ORCID,Mouriès-Mansuy Virginie¹^ORCID,Fensterbank Louis³^ORCID

Affiliation:

1. Sorbonne Université, CNRS, Institut Parisien de Chimie Moléculaire, 4 place Jussieu, 75005 Paris, France

2. Department of Chemistry, University of Helsinki, 00014 Helsinki, Finland

3. Collège de France, Université PSL, Institut Parisien de Chimie Moléculaire, Sorbonne Université, CNRS, 4 place Jussieu, 75005 Paris, France

Funder

Coll?ge de France

Centre National de la Recherche Scientifique

Sorbonne Universit?

Institut Universitaire de France

LabEx MiChem

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02003

Reference31 articles.

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4. Using Triethynylphosphine Ligands Bearing Bulky End Caps To Create a Holey Catalytic Environment: Application to Gold(I)-Catalyzed Alkyne Cyclizations

5. Confinement‐Induced Selectivities in Gold(I) Catalysis—The Benefit of Using Bulky Tri‐( ortho ‐biaryl)phosphine Ligands