Lipase-catalyzed enantio- and regioselective transformation of 3-epi-shikimic acid derivatives as the key step for the entry of polyoxygenated carbacycles-Reference-Cited by-同舟云学术

Lipase-catalyzed enantio- and regioselective transformation of 3-epi-shikimic acid derivatives as the key step for the entry of polyoxygenated carbacycles

Published:2010-11 Issue:1-2 Volume:67 Page:78-84
ISSN:1381-1177
Container-title:Journal of Molecular Catalysis B: Enzymatic
language:en
Short-container-title:Journal of Molecular Catalysis B: Enzymatic

Author:

Hamada Manabu,Higashi Toshinori,Shoji Mitsuru,Umezawa Kazuo,Sugai Takeshi

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference13 articles.

1. Regioselective Enzymatic Acylation of Methyl Shikimate. Influence of Acyl Chain Length and Solvent Polarity on Enzyme Specificity

2. Enzyme-catalyzed resolution of 3,8-dioxatricyclo[3.2.1.02,4]octane-6-carboxylic esters and the application to the synthesis of 3-epishikimic acid

3. Influence of intramolecular hydrogen bonds in the enzyme-catalyzed regioselective acylation of quinic and shikimic acid derivatives

4. An Efficient Synthesis of a Potential (−)-Reserpine Intermediate from (−)-Shikimic Acid of the Chiral Pool

5. Chemistry of shikimic acid derivatives. Synthesis of specifically labelled shikimic acid at C-3 or C-4

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