Sabitha, Gowravaram ; Srinivas Reddy, Ch. ; Srihari, Pabbaraja ; Yadav, Jhillu Singh (2003) Stereoselective total synthesis of (+)-Virol C Synthesis, 2003 (17). pp. 2699-2704. ISSN 0039-7881
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Official URL: http://www.thieme-connect.com/ejournals/abstract/s...
Related URL: http://dx.doi.org/10.1055/s-2003-42465
Abstract
A highly stereoselective synthesis of (+)-Virol C (1) has been achieved starting from octan-1-ol (6) using two different strategies, elimination reactions of epoxyallyl chloride 12 and epoxy chloride 16 to hydroxyenyne 2 and trans-hydroxyalkenyl chloride 4 as key reactions in route a and route b, respectively.
Item Type: | Article |
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Source: | Copyright of this article belongs to Thieme Medical Publishers. |
Keywords: | Virol C; Stereoselective; Elimination Reaction; Cadiot-Chodkiewicz Coupling; Sonogashira |
ID Code: | 63092 |
Deposited On: | 28 Sep 2011 03:20 |
Last Modified: | 28 Sep 2011 03:20 |
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