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- W2511348839 abstract "An efficient and highly stereocontrolled synthesis of protected (2R,3R,4S)-3-hydroxy-2,4,6-trimethylheptanoic acid, the β-hydroxy acid unit that acylates the N-terminus of callipeltin A, has been devised starting from methyl (2S)-2-methyl-3-hydroxypropionate. Comparison of NMR data with the corresponding fragment obtained from the acid hydrolysate of callipeltin A indicates that the stereostructure of the above fragment should be revised." @default.
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- W2511348839 date "2002-05-01" @default.
- W2511348839 modified "2023-10-09" @default.
- W2511348839 title "Synthetic studies on callipeltin A: stereoselective synthesis of (2 R ,3 R ,4 S )-3-hydroxy-2,4,6-trimethylheptanoic acid" @default.
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- W2511348839 doi "https://doi.org/10.1016/s0957-4166(02)00178-7" @default.
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