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The first synthesis of marine sesterterpene (+)-scalarolide

✍ Scribed by Xiang-Jian Meng; Yang Liu; Wen-Yuan Fan; Bin Hu; Wenting Du; Wei-Ping Deng


Book ID
104096710
Publisher
Elsevier Science
Year
2009
Tongue
French
Weight
332 KB
Volume
50
Category
Article
ISSN
0040-4039

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✦ Synopsis


The synthesis of the first example of C12 oxygenated marine scalaranic sesterterpenes (+)-scalarolide was achieved through three key steps including the ring-opening rearrangement of epoxide, stereoselective Diels-Alder addition and one-pot c-butenolide formation process, and the absolute configuration of natural scalarolide was confirmed.


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