Recognition of the remote chiral center in lipase-catalyzed kinetic resolution of [2-methyl-2-(2′-naphthyl)-1,3-benzodioxol-4-yl]methyl acetate, the precursor of 2-methyl-2-(2′-naphthyl)-1,3-benzodioxole-4-carboxylic acid (MNB carboxylic acid)-Reference-Cited by-同舟云学术

Recognition of the remote chiral center in lipase-catalyzed kinetic resolution of [2-methyl-2-(2′-naphthyl)-1,3-benzodioxol-4-yl]methyl acetate, the precursor of 2-methyl-2-(2′-naphthyl)-1,3-benzodioxole-4-carboxylic acid (MNB carboxylic acid)

Published:2014-11 Issue: Volume:109 Page:130-135
ISSN:1381-1177
Container-title:Journal of Molecular Catalysis B: Enzymatic
language:en
Short-container-title:Journal of Molecular Catalysis B: Enzymatic

Author:

Natori Naoki,Nakagawara Kaoruko,Shoji Mitsuru,Sugai Takeshi,Hanaya Kengo^ORCID

Funder

Grant-in-Aid for Scientific Research

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference13 articles.

1. Biological Sciences and Analytical Chemistry. Development of a new chiral derivatizing reagent, (+)-2-methyl-2-.BETA.-naphthyl-1,3-benzodioxole-4-carboxylic acid, for enantiomer analysis of amino acids.

2. Chemoenzymatic Synthesis of Both Enantiomers of 2-tert-Butyl-2-methyl-1,3-benzodioxole-4-carboxylic (TBMB) Acid

3. Lipase-catalyzed asymmetric hydrolysis of esters having remote chiral/prochiral centers

4. Lipase-catalyzed enantioselective deacetylation of ortho-substituted phenyl acetates with 1-butanol in organic solvents

5. CHARMM: A program for macromolecular energy, minimization, and dynamics calculations

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