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- W2054739667 abstract "Cyclo-[3α-(phenylalaninylamino)-5β-cholanate]22 was synthesized from lithocholic acid and (S)-phenylalanine. The synthesis requires three transformations: i) stereoselective conversion of the 3α-hydroxy group to the 3α-amino group; ii) preparation of the linear steroidal peptide; iii) cyclodimerisation. NMR measurements and MM3 calculations support a conformation of 2 with a lipophilic cavity." @default.
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- W2054739667 title "A steroidal cyclopeptide, synthesis and shape of the cavity" @default.
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- W2054739667 doi "https://doi.org/10.1016/s0040-4039(00)75839-4" @default.
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