Organocatalytic regio- and enantioselective C1-arylation of β,γ-alkynyl-α-imino esters with pyrrolo[2,1-<i>a</i>]isoquinolines-Reference-Cited by-同舟云学术

Organocatalytic regio- and enantioselective C1-arylation of β,γ-alkynyl-α-imino esters with pyrrolo[2,1-a]isoquinolines

Published:2024 Issue:7 Volume:60 Page:831-834
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhang Xuan¹,Song Xiaoxiao¹,Ni Qijian¹^ORCID

Affiliation:

1. College of Chemistry and Materials Science, Key Laboratory of Functionalized Molecular Solids, Ministry of Education, Anhui Laboratory of Molecule-Based Materials, Anhui Normal University, Wuhu, Anhui 241002, P. R. China

Abstract

CPA-catalyzed regio- and enantioselective arylation of β,γ-alkynyl-α-imino esters with pyrroloisoquinolines has been developed, affording axially chiral tetrasubstituted allenoates.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Anhui Province

Anhui Provincial Department of Education

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D3CC04946A

Reference73 articles.

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