Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/447
Title: | Justicia lignans: Part 10† _ Synthesis of tiruneesiin, the first neolignan from Justicia species |
Authors: | Subbaraju, Gottumukkala V Kavitha, Jakka |
Keywords: | Ttiruneesiin;Neolignan;Synthesis;Oxidative dimerization;Justicia neesii |
Issue Date: | Feb-2008 |
Publisher: | CSIR |
IPC Code: | Int.Cl.⁸ C07D |
Abstract: | (±)-Tiruneesiin, 3-[2-(4–hydroxy–3-methoxyphenyl)-3-aceto¬xy¬methyl-7-methoxy-2, 3-dihydro-1-benzofuran-5-yl]propan-1-yl acetate 1, is synthesized starting from methyl ferulate 2 with an overall yield of 12.6﹪. Ag₂O induced dimerization of 2 is used as a key step in the synthesis. |
Page(s): | 357-359 |
ISSN: | 0376-4699 |
Appears in Collections: | IJC-B Vol.46B(02) [February 2007] |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
IJCB 46B(2) (2007) 357-359.pdf | 46.46 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.