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- W2102287390 abstract "The enantiomerically pure methyl ester of the complete larger hydroxy acid (C(1)C(18)) of the macrodiolide antibiotic pamamycin-607 has been synthesized using a general sultone route to actic acids and analogs. The requisite N,N-dimethylamino moiety was introduced by Mitsunobu inversion with hydrazoic acid followed by a reaction cascade involving hydrogenation and double reductive methylation." @default.
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- W2102287390 date "2000-09-01" @default.
- W2102287390 modified "2023-10-01" @default.
- W2102287390 title "Enantioselective synthesis of the larger fragment of pamamycin-607" @default.
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- W2102287390 doi "https://doi.org/10.1016/s0040-4039(00)01308-3" @default.
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