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Stereoselective dioxygenase-catalysed benzylic hydroxylation at prochiral methylene groups in the chemoenzymatic synthesis of enantiopure vicinal aminoindanols.
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UNSPECIFIED (1996) Stereoselective dioxygenase-catalysed benzylic hydroxylation at prochiral methylene groups in the chemoenzymatic synthesis of enantiopure vicinal aminoindanols. TETRAHEDRON-ASYMMETRY, 7 (6). pp. 1559-1562. ISSN 0957-4166.
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Abstract
Enantiopure benzylic alcohols containing two stereogenic centres in a cis-relationship result from stereoselective monohydroxylation of achiral 2-substituted indans in cultures of Pseudomonas putida UV4 and are used in the chemoenzymatic synthesis of both cis- and trans-aminoindanol enantiomers. (C) 1996 Elsevier Science Ltd
Item Type: | Journal Article | ||||
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Subjects: | Q Science > QD Chemistry | ||||
Journal or Publication Title: | TETRAHEDRON-ASYMMETRY | ||||
Publisher: | PERGAMON-ELSEVIER SCIENCE LTD | ||||
ISSN: | 0957-4166 | ||||
Official Date: | June 1996 | ||||
Dates: |
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Volume: | 7 | ||||
Number: | 6 | ||||
Number of Pages: | 4 | ||||
Page Range: | pp. 1559-1562 | ||||
Publication Status: | Published |
Data sourced from Thomson Reuters' Web of Knowledge
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