The chemistry of O-silylated ketene acetals: an efficientstereocontrolled synthesis of N-benzoyl L-daunosamine

Tetrahedron Letters

Volumn 28, Issue 13, 1987, Pages 1431-1434

  Kita, Yasuyuki ^a   Itoh, Fumio ^a   Tamura, Osamu ^a   Ke, Ya Yuan ^a   Tamura, Yasumitsu ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000604066     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)95946-X     Document Type: Article

References (27)

1. Daunomycin. I. The Structure of Daunomycinone
2. New acyclic apporach to 3-amino-2,3,6-trideoxy-L-hexoses: a stereocontrolled synthesis of N-benzoyl L-daunosamine
3. Stereoselective synthesis of L-daunosamine.
4. Stereospecific synthesis of racemic daunosamine. Diastereofacial selectivity in a nitrone cycloaddition
5. Carbon-carbon bond forming reaction assisted by silicon transfer. The reaction between nitrones and ketene silyl acetals.
6. Synthesis of Precursors to L-Ristosamine and L-Daunosamine from L-Lactic Acid.
7. A stereoselective synthesis of N-benzoyl L-daunosamine.
8. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones