Kumari, D. ; Mukerjee, S. K. ; Seshadri, T. R. (1966) Synthesis of (±)-latifolin dimethyl ether Tetrahedron, 22 (10). pp. 3491-3499. 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)92537-2
Abstract
(±)-Latifolin dimethyl ether has been synthesized by coupling 1,2,4-trimethoxybenzene and o-methoxycinnamyl cation. The isomeric benzylstyrene is also a product of the reaction. Among the possible biogenetic routes for the related compounds present in Dalbergia latifolia the most likely steps seem to be phenylcinnamic esters and 4-phenylcoumarins followed by stages of reduction. The alternative of cinnamyl cation functioning will limit the biosynthesis only to latifolin type of compounds.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 68148 |
| Deposited On: | 02 Nov 2011 11:27 |
| Last Modified: | 02 Nov 2011 11:27 |
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