Microbial hydroxylation of unsaturated, cyclic carboxylic acids protected as benzoxazoles
Author:
Publisher
Elsevier BV
Subject
Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis
Reference10 articles.
1. Microbial hydroxylation of 2-cycloalkylbenzoxazoles. Part I. Product spectrum obtained from Cunninghamella blakesleeana DSM 1906 and Bacillus megaterium DSM 32
2. Microbial hydroxylation of 2-cycloalkylbenoxazoles. Part II. Determination of product structures and enhancement of enantiomeric excess
3. Microbial hydroxylation of 2-cycloalkylbenzoxazoles. Part III. Determination of product enantiomeric excess and cleavage of benzoxazoles
4. Stereospecific Biohydroxylations of Protected Carboxylic Acids with Cunninghamella blakesleeana
5. The Concept of Docking/Protecting Groups in Biohydroxylation
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2. Nitrile Biotransformations for the Synthesis of Highly Enantioenriched β-Hydroxy and β-Amino Acid and Amide Derivatives: A General and Simple but Powerful and Efficient Benzyl Protection Strategy To Increase Enantioselectivity of the Amidase;The Journal of Organic Chemistry;2008-05-07
3. Dramatic Enhancement of Enantioselectivity of Biotransformations of β-Hydroxy Nitriles Using a Simple O-Benzyl Protection/Docking Group;Organic Letters;2006-06-22
4. Lactones 27 [1]: Transformations of γ-lactones fused to a dimethylcyclohexane ring in Absidia cylindrospora cultures;Journal of Molecular Catalysis B: Enzymatic;2006-05
5. The use of substrate engineering in biohydroxylation;Current Opinion in Biotechnology;2002-12
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