P-60 Synthetic Study of 13-Oxyingenol(Poster Presentation)
-
- Ohyoshi Takayuki
- Graduate School of Pure and Applied Sciences, University of Tsukuba
-
- Miyazawa Yamato
- Graduate School of Pure and Applied Sciences, University of Tsukuba
-
- Haruna Toshihiro
- Graduate School of Pure and Applied Sciences, University of Tsukuba
-
- Asuma Yuki
- Graduate School of Pure and Applied Sciences, University of Tsukuba
-
- Aoki Kenta
- Graduate School of Pure and Applied Sciences, University of Tsukuba
-
- Ohmura Satomi
- Graduate School of Pure and Applied Sciences, University of Tsukuba
-
- Hayakawa Ichiro
- Graduate School of Pure and Applied Sciences, University of Tsukuba
-
- Kigoshi Hideo
- Graduate School of Pure and Applied Sciences, University of Tsukuba
Bibliographic Information
- Other Title
-
- P-60 抗HIV活性物質13-オキシインゲノールの合成研究(ポスター発表の部)
Abstract
13-Oxyingenol (1) and ingenol (2) are diterpenoids isolated from the plants of Euphorbia sp. They and their analogs have interesting bioactivities. Particularly, 13-oxyingenol derivatives such as RD4-2138 have a strong anti-HIV activity. The structural features of ingenol and 13-oxyingenol are a high degree of oxygenation and a highly strained inside-outside bicylcic ring system. The molecular complexity of ingenol derivatives, in conjunction with their potent biological activities, has made them attractive synthetic targets. We planed the synthesis of 13-oxyingenol (1) by using ring-closing olein metathesis strategy. The starting point for this work was the construction of the β-ketoester 3 from 2-(4-hydroxyphenyl)ethanol. We stereoselectively introduced the methyl group to C-11 by using diastereoselective hydrogenation, to give β-ketoester 3 with desired stereochemistry. Then, we achieved the construction of the full carbon framework of 13-oxyingenol by using intramolecular spirocyclization and ring closing olefin metathesis as key steps. Further approach to 13-oxyingenol is currently underway in our group and will be reported in the symposium.
Journal
-
- Symposium on the Chemistry of Natural Products, symposium papers
-
Symposium on the Chemistry of Natural Products, symposium papers 50 (0), 719-724, 2008
Symposium on the Chemistry of Natural Products Steering Committee
- Tweet
Details 詳細情報について
-
- CRID
- 1390001206078484736
-
- NII Article ID
- 110007066659
-
- ISSN
- 24331856
-
- Text Lang
- ja
-
- Data Source
-
- JaLC
- CiNii Articles
-
- Abstract License Flag
- Disallowed