Organocatalytic Atroposelective Synthesis of N−N Axially Chiral Indoles and Pyrroles by De Novo Ring Formation-Reference-Cited by-同舟云学术

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Organocatalytic Atroposelective Synthesis of N−N Axially Chiral Indoles and Pyrroles by De Novo Ring Formation

Published:2022-02-23 Issue:17 Volume:134 Page:
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angewandte Chemie

Author:

Chen Ke‐Wei¹,Chen Zhi‐Han¹,Yang Shuang¹,Wu Shu‐Fang¹,Zhang Yu‐Chen¹,Shi Feng¹^ORCID

Affiliation:

1. School of Chemistry and Materials Science Jiangsu Normal University Xuzhou 221116 China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202116829

Reference184 articles.

1. Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products

2. For reviews:

3. Assessing Atropisomer Axial Chirality in Drug Discovery and Development

4. Atropisomerism in medicinal chemistry: challenges and opportunities

5. Privileged Chiral Ligands and Catalysts

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1. Enantioselective synthesis of 6-(Indole-2-yl)-3,4-dihydropyran-2-one skeletons by N-Heterocyclic carbene-catalyzed asymmetric [3 + 3] cycloaddition of α-bromocinnamaldehyde;Chemical Synthesis;2023-07-21

2. Catalytic Asymmetric Synthesis of Axially Chiral Diaryl Ethers through Enantioselective Desymmetrization;Angewandte Chemie International Edition;2023-02-24

3. Catalytic Asymmetric Synthesis of Axially Chiral Diaryl Ethers through Enantioselective Desymmetrization;Angewandte Chemie;2023-02-24

4. Organocatalytic Enantioselective Synthesis of Axially ChiralN,N′‐Bisindoles;Angewandte Chemie International Edition;2023-02-21

5. Organocatalytic Enantioselective Synthesis of Axially ChiralN,N′‐Bisindoles;Angewandte Chemie;2023-02-21

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