Synthesis of (±)duryne
✍ Scribed by V.H. Deshpande; B.K. Upadhye; R.D. Wakharkar
- Book ID
- 104229784
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 149 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Synthesis of cytotoxic metabolite, duryne (l), involving symmetrical synthetic strategy is described. There has been considerable growth in the newly discovered biologically active marine natural products in the last decade'. Recently, Wright et al.' reported the isolation of duryne (I) from marine sponge Cribrachalina dura which inhibits the growth of a number of in vitro tumour cell lines. The structure of duryne was established on the basis of spectroscopic analysis as a symmetrical CjO dial, consisting of two terminal acetylenic groups,two asymmetric centres and three olefinic bands. Although the geometry of two double bonds at C4 and C4', is E, the geometry
📜 SIMILAR VOLUMES
Duryne, 1, a cytotoxic metabolite which inhibits the growth of both mouse and human tumor cell lines in vitro has been isolated from the marine sponge Cribrochalina dura. Its -structure has been assigned by spectral methods.
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