Applications of Baylis-Hillman chemistry: Enantioselective synthesis of (-)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy
Applications of Baylis-Hillman chemistry: Enantioselective synthesis of (-)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy
| dc.contributor.author | Basavaiah, Deevi | |
| dc.contributor.author | Kumaragurubaran, Nagaswamy | |
| dc.contributor.author | Sharada, Duddu S. | |
| dc.contributor.author | Reddy, Ravi Mallikarjuna | |
| dc.date.accessioned | 2022-03-27T09:03:05Z | |
| dc.date.available | 2022-03-27T09:03:05Z | |
| dc.date.issued | 2001-09-17 | |
| dc.description.abstract | Asymmetric synthesis of (-)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates in 25-40% enantiomeric purities via the reaction of methyl (2Z)-3-aryl-2-(bromomethyl)prop-2-enoates with prop-2-yn-1-ol in the presence of quinidine is described. © 2001 Elsevier Science Ltd. All rights reserved. | |
| dc.identifier.citation | Tetrahedron. v.57(38) | |
| dc.identifier.issn | 00404020 | |
| dc.identifier.uri | 10.1016/S0040-4020(01)00786-4 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/abs/pii/S0040402001007864 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/12333 | |
| dc.subject | Baylis-Hillman chemistry | |
| dc.subject | Chiral leaving group | |
| dc.subject | Methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates | |
| dc.title | Applications of Baylis-Hillman chemistry: Enantioselective synthesis of (-)-methyl 3-aryl-2-methylene-3-(prop-2-yn-1-yloxy)propanoates via chiral leaving group strategy | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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