Preparation of aminosaccharides using ester-imine condensations: syntheses of methyl -benzoylacosaminide and methyl -[oxo(phenylmethoxy) acetyl)daunosaminide from (S)-ethyl 3-hydroxybutyrate-Reference-Cited by-同舟云学术

Preparation of aminosaccharides using ester-imine condensations: syntheses of methyl -benzoylacosaminide and methyl -[oxo(phenylmethoxy) acetyl)daunosaminide from (S)-ethyl 3-hydroxybutyrate

Published:1989-01 Issue:5 Volume:45 Page:1283-1292
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Gallucci Judith C.,Ha Deok-Chan,Hart David J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference43 articles.

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2. N-Trimethylsilylimines: applications to the syntheses of .beta.-lactams

3. Asymmetric synthesis of (1'R,3R,4R)-4-acetoxy-3-[1'-((tert-butyldimethylsilyl)oxy)ethyl]-2-azetidinone and other 3-(1'-hydroxyethyl)-2-azetidinones from (S)-(+)-ethyl 3-hydroxybutanoate: formal total synthesis of (+)-thienamycin

4. A FACILE ENTRY TO 3-(1-HYDROXYETHYL)-2-AZETIDINONES FROM METHYL (R)-3-HYDROXYBUTANOATE BASED ON THE ESTER ENOLATE-ALDIMINE CONDENSATION

5. Stereocontrolled total synthesis of the chiral building block (3S,4R)-3- [(R)-1-hydroxyethyl]-4-acetyloxy-azetidin-2-one: a useful synthon for the synthesis of (+)-thienamycin, carbapenems and penems.

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