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- W2015586787 abstract "An efficient and stereoselective synthesis of the entire C27–C45 moiety of lagunamide A has been achieved from 1-[(4S)-4-benzyl-2-thioxothiazolidin-3-yl]propan-1-one in six steps with 22% overall yield. The key step in the synthesis is an asymmetric acetal aldol reaction featuring the enantioselective addition of a chiral thiazolidinethione-derived titanium enolate to an acetal to establish the stereochemistry at C39." @default.
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- W2015586787 date "2014-01-01" @default.
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- W2015586787 title "An efficient synthesis of the C27–C45 fragment of lagunamide A, a cyclodepsipeptide with potent cytotoxic and antimalarial properties" @default.
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- W2015586787 doi "https://doi.org/10.1016/j.tetasy.2013.11.020" @default.
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