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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
Full text not available from this repository.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 |
|---|---|
| Subjects: | Q Science > QD Chemistry |
| Journal or Publication Title: | TETRAHEDRON-ASYMMETRY |
| Publisher: | PERGAMON-ELSEVIER SCIENCE LTD |
| ISSN: | 0957-4166 |
| Date: | June 1996 |
| Volume: | 7 |
| Number: | 6 |
| Number of Pages: | 4 |
| Page Range: | pp. 1559-1562 |
| Publication Status: | Published |
| URI: | http://wrap.warwick.ac.uk/id/eprint/18751 |
Data sourced from Thomson Reuters' Web of Knowledge
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