Nayak, U. R. ; Kapadi, A. H. ; Sukh Dev, (1970) Thermal reorganisation reactions-II: Thermal cyclization of methyl kamlolenate Tetrahedron, 26 (21). pp. 5083-5086. ISSN 0040-4020
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Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/S0040-4020(01)93161-8
Abstract
Sulphur-catalysed intramolecular thermal cyclization of conjugated trienes, discovered with methyl eleostearate, has now been extended to its ω-hydroxy analogue, viz. methyl kamlolenate. The primary cyclic monomer (III) has been isolated and characterised. Two cyclokamlolenate-derived macrocyclic lactones (Vl) and (VII) have also been prepared.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Methyl Kamlolenate-sulphur-catalysed Intramolecular Thermal Cyclization Of; Methyl Cyclokamlolenate-I; Macrocyclic Lactones (ar-cyclokamlolactone and Saturated Cyclokamlolactone) |
| ID Code: | 59142 |
| Deposited On: | 03 Sep 2011 11:45 |
| Last Modified: | 03 Sep 2011 11:45 |
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