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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


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