Highly efficient synthesis of (R)-1,3-butanediol via anti-Prelog reduction of 4-hydroxy-2-butanone with absolute stereoselectivity by a newly isolated Pichia kudriavzevii-Reference-Cited by-同舟云学术

Highly efficient synthesis of (R)-1,3-butanediol via anti-Prelog reduction of 4-hydroxy-2-butanone with absolute stereoselectivity by a newly isolated Pichia kudriavzevii

Published:2020-08 Issue:8 Volume:28 Page:2160-2166
ISSN:1004-9541
Container-title:Chinese Journal of Chemical Engineering
language:en
Short-container-title:Chinese Journal of Chemical Engineering

Author:

Zu Han,Zhang Hui,Fan Anwen,Gu Jie,Nie Yao,Luo Pengjie,Xu Yan

Funder

National Key R&D Program of China

National Natural Science Foundation of China

111 Project

High-end Foreign Experts Recruitment Program

Jiangsu Province

National Program for Support of Top-notch Young Professionals

Fundamental Research Funds for the Central Universities

Priority Academic Program Development of Jiangsu Higher Education Institutions

Jiangsu Higher Education Institutions

National First-Class Discipline Program of Light Industry Technology and Engineering

Publisher

Elsevier BV

Subject

General Chemical Engineering,General Chemistry,Biochemistry,Environmental Engineering

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4. Synthesis of two stereoisomers of the propanoate ester of 8-methyl-2-decanol using remote asymmetric induction;Ferrelra;Tetrahedron.,1990

5. Cheminform abstract: a facile conversion of the phenylthio group to acetoxy by copper reagents for a practical synthesis of 4-acetoxyazetidin-2-one derivatives from (R)-butane-1,3-diol;Nakatsuka;Cheminform.,1991

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