Hydroboration of prochiral olefins with chiral Lewis base-borane complexes: Relationship to the mechanism of hydroboration
Hydroboration of prochiral olefins with chiral Lewis base-borane complexes: Relationship to the mechanism of hydroboration
| dc.contributor.author | Narayana, Chatla | |
| dc.contributor.author | Periasamy, Mariappan | |
| dc.date.accessioned | 2022-03-27T09:12:58Z | |
| dc.date.available | 2022-03-27T09:12:58Z | |
| dc.date.issued | 1987-12-01 | |
| dc.description.abstract | Alcohols with up to 19% enantiomeric excess were obtained on hydroboration/oxidation of representative prochiral olefins using N-isobornyl-N-methylaniline-borane or N-benzyl-N-isopropyl-α- methylbenzylamine-borane indicating that the Lewis base is present in the hydroboration transition state. | |
| dc.identifier.citation | Journal of the Chemical Society, Chemical Communications | |
| dc.identifier.issn | 00224936 | |
| dc.identifier.uri | 10.1039/C39870001857 | |
| dc.identifier.uri | http://xlink.rsc.org/?DOI=C39870001857 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12597 | |
| dc.title | Hydroboration of prochiral olefins with chiral Lewis base-borane complexes: Relationship to the mechanism of hydroboration | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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