Lipase TL®-mediated kinetic resolution of glycerol analogues: Efficient convergent route to both enantiomeric glycerol units-Reference-Cited by-同舟云学术

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Lipase TL®-mediated kinetic resolution of glycerol analogues: Efficient convergent route to both enantiomeric glycerol units

Published:2021-06 Issue: Volume:73 Page:153138
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Aoyagi Yutaka,Nomura Shoko,Horiba Karen,Shikano Rina,Omura Yumi,Omiya Hiroko,Fukuzawa Sanae,Yano Reiko,Williams Robert M.,Takeya Koichi,Hitotsuyanagi Yukio

Funder

Japan Society for the Promotion of Science

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Practical syntheses of (R)- and (S)-1-alkylamino-3-aryloxy-2-porpanols from a single carbohydrate precursor.

2. Total synthesis of (R)-glycerol acetonide and the antiepileptic and hypotensive drug (-)-.gamma.-amino-.beta.-hydroxybutyric acid (GABOB): use of vitamin C as a chiral starting material

3. Asymmetric epoxidation of allyl alcohol: efficient routes to homochiral .beta.-adrenergic blocking agents

4. Lipases in the preparation of β-blockers

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