Catalytic asymmetric aldol reaction of the silyl enol ether of acetic acid thioester with aldehydes using chiral tin(II) Lewis acid

Tetrahedron: Asymmetry

Volumn 2, Issue 7, 1991, Pages 635-638

  Kobayashi, Shu ^a   Furuya, Minoni ^a   Ohtsubo, Akihiro ^a   Mukaiyama, Teruaki ^a  

^a TOKYO UNIVERSITY OF SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ESTER; THIOESTER;

ARTICLE; CHEMICAL STRUCTURE; REACTION ANALYSIS; SYNTHESIS;

EID: 0025813363     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/S0957-4166(00)86116-9     Document Type: Article

References (19)

1. Stereoselective Aldol Reactions withα-Unsubstituted Chiral Enolates
2. Stereoselective Aldol Reactions withα-Unsubstituted Chiral Enolates
3. Asymmetric aldol reaction of silyl enol ethers with aldehydes promoted by the combined use of chiral diamine coordinated tin(II) triflate and tributyltin fluoride.
4. Perfect stereochemical control in the synthesis of syn-.ALPHA.-methyl-.BETA.-hydroxy thioesters by asymmetric aldol reaction of silyl enol ethers with aldehydes.
5. An efficient chiral promoter in the aldol-type reaction. Chiral diamine coordinated tin(II) triflate-dibutyltindiacetate complex.
6. Catalytic asymmetric aldol reaction of silyl enol ethers with aldehydes by the use of chiral diamine coordinated tin(II) triflate.
7. The efficient catalytic asymmetric aldol-type reaction.
8. Synthesis of .eta.1 oxygen-bound rhodium enolates. Applications to catalytic aldol chemistry
9. A new efficient chiral catalyst system. Combined use of tin(II) oxide, trimethylsilyl triflate and chiral diamine in the asymmetric aldol reaction.
10. (1,1'-Bi-2-naphthalenediolato(2-)-O,O')oxotitanium. An efficient chiral catalyst for the asymmetric aldol reaction of silyl enol ethers with aldehydes.
11. Catalytic asymmetric aldol reaction of ketene silyl acetals with aldehydes by use of chiral bissulfonamido zinc(II).