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An Efficient Stereoselective Total Synthesis of Synargentolide A and Its Epimer

✍ Scribed by Biswanath Das; Penagaluri Balasubramanyam; Boyapati Veeranjaneyulu; Gandolla Chinna Reddy


Publisher
John Wiley and Sons
Year
2011
Tongue
German
Weight
132 KB
Volume
94
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The stereoselective total synthesis of a naturally occurring α‐pyrone (=2__H__‐pyran‐2‐one) derivative, synargentolide A (1), and of its epimer 2 (with the originally proposed structure of synargentolide A) was efficiently accomplished involving D‐tartaric acid as the starting material and an olefin cross‐metathesis reaction as the key step.


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