Attrition‐Enhanced Deracemization of Axially Chiral Nicotinamides-Reference-Cited by-同舟云学术

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Attrition‐Enhanced Deracemization of Axially Chiral Nicotinamides

Published:2020-02-18 Issue:8 Volume:2020 Page:1001-1005
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Ishikawa Hiroki¹,Ban Kazuma¹,Uemura Naohiro¹,Yoshida Yasushi¹²^ORCID,Mino Takashi¹²^ORCID,Kasashima Yoshio³,Sakamoto Masami¹²^ORCID

Affiliation:

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

2. Molecular Chirality Research Center Graduate School Engineering Chiba University Yayoi‐cho, Inage‐ku 263‐8522 Chiba Japan

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

Funder

Japan Science and Technology Agency

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.201901826

Reference48 articles.

1. Stereospecificity for Nicotinamide Nucleotides in Enzymatic and Chemical Hydride Transfer Reaction

2. Enzymes as Catalysts in Synthetic Organic Chemistry [New Synthetic Methods (53)]

3. Enzyme in der organischen Synthese

4. Regeneration of nicotinamide cofactors for use in organic synthesis

5. Enzymes for chemical synthesis

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1. Shortcut model to evaluate the performance of continuous preferential crystallization for conglomerates forming chiral systems;Chemical Engineering Science;2024-11

2. Conglomerate Crystallization in the Cambridge Structural Database (2020–2021);Crystal Growth & Design;2023-03-22

3. Recent advances in the field of chiral crystallization;Chirality;2022-07-29

4. Shortcut Model for Batch Preferential Crystallization Coupled with Racemization for Conglomerate-Forming Chiral Systems;Crystal Growth & Design;2022-06-06

5. Attrition‐Enhanced Asymmetric Transformation of Axially Chiral Nicotinamides by Dynamic Chiral Salt Formation;ChemPlusChem;2022-01

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