ICAR Research Data Repository for Knowledge Management
The formation of novel 1,3-dioxolanes: atypical Baylis–Hillman reaction of a sesquiterpene lactone parthenin
IR@CSIR-IIIM
View Archive Info| Field | Value | |
| Title |
The formation of novel 1,3-dioxolanes: atypical Baylis–Hillman reaction of a sesquiterpene lactone parthenin
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| Creator |
Shah, Bhahwal A.
Taneja, Subhash C. Sethi, Vijay K. Gupta, Pankaj Andotra, Samar S. Chimni, Swapandeep S. Qazi, Ghulam N. |
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| Subject |
Chemical Sciences
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| Description |
The Baylis–Hillman reaction of a sesquiterpene lactone parthenin with various aldehydes gave unexpected products containing a 1,3-dioxolane moiety. Both small aliphatic and aromatic aldehydes produced 1,3-dioxolanes, whereas higher aliphatic aldehydes produced normal Baylis–Hillman products.
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| Date |
2007
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| Type |
Article
PeerReviewed |
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| Format |
application/pdf
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| Identifier |
http://iiim.csircentral.net/362/1/10.1016j.tetlet.2006.12.019.pdf
Shah, Bhahwal A. and Taneja, Subhash C. and Sethi, Vijay K. and Gupta, Pankaj and Andotra, Samar S. and Chimni, Swapandeep S. and Qazi, Ghulam N. (2007) The formation of novel 1,3-dioxolanes: atypical Baylis–Hillman reaction of a sesquiterpene lactone parthenin. Tetrahedron Letters, 48 (6). pp. 955-960. ISSN 00404039 |
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| Relation |
http://dx.doi.org/10.1016/j.tetlet.2006.12.019
http://iiim.csircentral.net/362/ |
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