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Synthetic studies toward the construction of the cis-decalin portion of superstolides A and B. Application of a sequential double michael reaction and an anionic oxy-Cope rearrangement
Authors:Hua Zhengmao  Yu Wensheng  Su Mei  Jin Zhendong
Institution:Division of Medicinal and Natural Products Chemistry, College of Pharmacy, The University of Iowa, Iowa City, 52242, USA.
Abstract:A highly convergent strategy for the asymmetric synthesis of the cis-decalin portion of the antitumor macrolide superstolide A was developed. The key reactions in our approach involve a sequential double Michael reaction and an anionic oxy-Cope rearrangement.
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