Alpha hydroxylation of carboxylic acids with molecular oxygen catalyzed by the 
alpha oxidase of peas (Pisum sativum): A novel biocatalytic synthesis of 
enantiomerically pure (R)-2-hydroxy acids

Adam, W.; Boland, Wilhelm; Hartmannschreier, J.; Humpf, H.-U.; Lazarus, M.; Saffert, A.; Saha-Möller, C. R.; Schreier, P.

doi:10.1021/ja981252r

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Alpha hydroxylation of carboxylic acids with molecular oxygen catalyzed by the alpha oxidase of peas (Pisum sativum): A novel biocatalytic synthesis of enantiomerically pure (R)-2-hydroxy acids

Adam, W., Boland, W., Hartmannschreier, J., Humpf, H.-U., Lazarus, M., Saffert, A., et al. (1998). Alpha hydroxylation of carboxylic acids with molecular oxygen catalyzed by the alpha oxidase of peas (Pisum sativum): A novel biocatalytic synthesis of enantiomerically pure (R)-2-hydroxy acids. Journal of the American Chemical Society, 120(43), 11044-11048. doi:10.1021/ja981252r.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-9E47-2 Version Permalink: https://hdl.handle.net/21.11116/0000-0009-3948-7

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Creators:
Adam, W., Author
Boland, Wilhelm¹, Author
Hartmannschreier, J., Author
Humpf, H.-U., Author
Lazarus, M., Author
Saffert, A., Author
Saha-Möller, C. R., Author
Schreier, P., Author

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1Department of Bioorganic Chemistry, Prof. Dr. W. Boland, MPI for Chemical Ecology, Max Planck Society, ou_24028

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Free keywords: Enantioselective oxidation Cucumis-sativus Fatty-acids Resolution Reduction Aldehydes Esters System. Chemistry. Chemistry & analysis.

Abstract: The substrate selectivities of the ct oxidation of saturated, unsaturated, and heteroatom-containing (oxygen, sulfur) carboxylic acids I by the enzyme extract of peas (Pisum sativum) indicate that this biotransformation proceeds highly enantioselectivel

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Dates: Date issued: 1998

Publication Status: Issued

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Identifiers: Other: BOL003
DOI: 10.1021/ja981252r

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Title: Journal of the American Chemical Society

Other : JACS

Abbreviation : J. Am. Chem. Soc.

Source Genre: Journal

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Publ. Info: Washington, DC : American Chemical Society

Pages: - Volume / Issue: 120 (43) Sequence Number: - Start / End Page: 11044 - 11048 Identifier: ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870