An enantioselective synthesis of the C(33)–C(37) fragment of Amphotericin B
نویسندگان
چکیده
منابع مشابه
An enantioselective synthesis of the C(33)-C(37) fragment of Amphotericin B.
An enantioselective synthesis of the C(33)-C(37) tripropionate fragment of Amphotericin B has been developed in only 6 steps.
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comparison of catalytic activity of heteropoly compounds in the synthesis of bis(indolyl)alkanes.
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15 صفحه اولAn enantioselective synthesis of the C24-C40 fragment of (-)-pulvomycin.
The C24-C40 fragment of (-)-pulvomycin was prepared in enantiomerically pure form using a concise synthesis method (15 linear steps from D-fucose, 6.8% overall yield) featuring a diastereoselective addition to an aldehyde, a β-selective glycosylation and a Stille cross-coupling as the key steps.
متن کاملModel studies on a diastereoselective synthesis of the C(33)–C(37) fragment of Amphotericin B
A new, short and highly diastereoselective synthetic route aiming at the C(33)–C(37) fragment of Amphotericin B has been developed. Studies with a model aldehyde (benzaldehyde) have given very promising results: the desired stereochemistry of all four stereocenters of the target molecule has been achieved with high diastereoselection. The stereochemistry of three key intermediates and the targe...
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ژورنال
عنوان ژورنال: Org. Biomol. Chem.
سال: 2003
ISSN: 1477-0520,1477-0539
DOI: 10.1039/b305845j