Attrition‐Enhanced Asymmetric Transformation of Axially Chiral Nicotinamides by Dynamic Chiral Salt Formation-Reference-Cited by-同舟云学术

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Attrition‐Enhanced Asymmetric Transformation of Axially Chiral Nicotinamides by Dynamic Chiral Salt Formation

Published:2022-01 Issue:1 Volume:87 Page:
ISSN:2192-6506
Container-title:ChemPlusChem
language:en
Short-container-title:ChemPlusChem

Author:

Nakamura Takumi¹,Ishikawa Hiroki¹,Ban Kazuma¹,Yoshida Yasushi¹^ORCID,Mino Takashi¹^ORCID,Kasashima Yoshio²^ORCID,Sakamoto Masami¹^ORCID

Affiliation:

1. Department of Applied Chemistry and Biotechnology Graduate School of Engineering Chiba University, Yayoi-cho, Inage-ku Chiba, Chiba 263-8522 Japan

2. Education Center, Faculty of Creative Engineering Chiba Institute of Technology Shibazono, Narashino Chiba 275-0023 Japan

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cplu.202100504

Reference77 articles.

1. For recent reviews and selected papers on axially chiral compounds see:

2. Recent Advances in Catalytic Asymmetric Construction of Atropisomers

3. Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products

4. Chiral Brønsted acids in enantioselective carbonyl activations – activation modes and applications

5. BINOL: A Versatile Chiral Reagent

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Stereochemical switch driven by crystallization: Interplay between stoichiometry and configuration of the products;Chirality;2022-04-26

2. Crystallization: A Tool for Asymmetric Synthesis and Isolation;Reference Module in Chemistry, Molecular Sciences and Chemical Engineering;2022

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