A STEREOCONTROLLED SYNTHESIS OF A KEY INTERMEDIATE TO (+)-THIENAMYCIN

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A formal synthesis of (+)-thienamycin was achieved by the enantioselective preparation of key intermediate azetidinone 2 [benzyl (2R,3S)-3-{(S)-1-hydroxyethyl}-4-oxo-2-azetidineacetate] via an intramolecular nitrone 1,3-dipolar cycloaddition.
Publisher
GEORG THIEME VERLAG
Issue Date
1991-07
Language
English
Article Type
Note
Keywords

DEHYDROPEPTIDASE-I; RENAL DIPEPTIDASE; THIENAMYCIN; ANTIBIOTICS; OXIDATION; ACIDS

Citation

SYNLETT, no.7, pp.520 - 522

ISSN
0936-5214
URI
http://hdl.handle.net/10203/56078
Appears in Collection
CH-Journal Papers(저널논문)
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