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A H-1-NMR METHOD FOR THE DETERMINATION OF ENANTIOMERIC EXCESS AND ABSOLUTE-CONFIGURATION OF CIS-DIHYDRODIOL METABOLITES OF POLYCYCLIC ARENES AND HETEROARENES
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UNSPECIFIED (1992) A H-1-NMR METHOD FOR THE DETERMINATION OF ENANTIOMERIC EXCESS AND ABSOLUTE-CONFIGURATION OF CIS-DIHYDRODIOL METABOLITES OF POLYCYCLIC ARENES AND HETEROARENES. TETRAHEDRON LETTERS, 33 (9). pp. 1241-1244. ISSN 0040-4039
Full text not available from this repository.Abstract
Metabolism of benzofuran and 2,3-dihydrobenzofuran by P.putida UV4 each yielded cis-dihydrodiols; catalytic hydrogenation of the cis-dihydrodiols obtained from polycyclic arenes and azaarenes followed by diMTPA ester formation (using both R- and S-MTPA) on the cis-tetrahydrodiols formed the basis of a H-1-NMR method for the determination of both enantiomeric excess and absolute configuration.
| Item Type: | Journal Article |
|---|---|
| Subjects: | Q Science > QD Chemistry |
| Journal or Publication Title: | TETRAHEDRON LETTERS |
| Publisher: | PERGAMON-ELSEVIER SCIENCE LTD |
| ISSN: | 0040-4039 |
| Date: | 25 February 1992 |
| Volume: | 33 |
| Number: | 9 |
| Number of Pages: | 4 |
| Page Range: | pp. 1241-1244 |
| Publication Status: | Published |
| URI: | http://wrap.warwick.ac.uk/id/eprint/22210 |
Data sourced from Thomson Reuters' Web of Knowledge
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