Kumari, Darshan ; Mukerjee, S. K. ; Seshadri, T. R. (1965) Constitution of latifolin Tetrahedron, 21 (6). pp. 1495-1499. 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)98312-7
Abstract
The positions of the hydroxy groups of latifolin have been established by preparing its ethyl ether and subjecting it to degradation in stages to (i) isolatifolin diethyl ether (ii) dimethoxy diethoxy benzophenone. The constitution of the benzophenone has been established by synthesis as 2,4-dimethoxy-2',5-diethoxybenzophenone. Using Grignard reaction the synthetic benzophenone has been converted into γ-(2,4-dimethoxy-5-ethoxyphenyl)-γ-(2'-ethoxyphenyl) propene which was identical with isolatifolin diethyl ether.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| ID Code: | 68133 |
| Deposited On: | 02 Nov 2011 11:27 |
| Last Modified: | 02 Nov 2011 11:27 |
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