133271-07-5

Upstream product

• 1374348-43-2 (S,E)-1-((R)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-phenylpent-4-en-1-one 
• 14371-10-9 (E)-3-phenylpropenal 
• 133270-84-5 (E)-5-(tert-Butyl-dimethyl-silanyloxy)-5-ethoxy-1-phenyl-pent-1-en-3-ol 

Downstream Products

• 1374348-45-4 N-methoxy-N-methyl-2-((2S,4R,6S)-2-phenyl-6-styryl-1,3-dioxan-4-yl)acetamide 
• 1374348-44-3 (Z)-ethyl 4-((2S,4S,6S)-2-phenyl-6-styryl-1,3-dioxan-4-yl)but-2-enoate 
• 91327-33-2 (S)-6-((S,E)-2-hydroxy-4-phenylbut-3-enyl)-5,6-dihydro-2H-pyran-2-one 
• 1374348-51-2 C₂₀H₂₀O₃ 
• 34427-30-0 (S,E)-1-((S)-6-oxo-3,6-dihydro-2H-pyran-2-yl)-4-phenylbut-3-en-2-yl acetate 
• 1374348-48-7 (S,2E,6E)-5-hydroxy-N-methoxy-N-methyl-7-phenylhepta-2,6-dienamide 
• 124781-38-0 1,3-Dihydroxy-5-phenyl-4-pentene 

Relevant academic research and scientific papers

Stereoselective total synthesis of (+)-(6R,2′S)-cryptocaryalactone and (-)-(6S,2′S)-epi cryptocaryalactone via asymmetric acetate aldol reaction

The total synthesis of (+)-(6R,2′S)-cryptocaryalactone and (-)-(6S,2′S)-epi cryptocaryalactone is reported based on asymmetric acetate aldol reaction. Still-Gennari reaction, Evans acetal intramolecular oxa-Michael reaction and lactonisation are the key s

Enantioselective Chiral Borane-Mediated Aldol Reactions of Silyl Ketene Acetals with Aldehydes. Novel Effect of the Trialkylsilyl Group of the Silyl Ketene Acetal on the Reaction Course

Highly enantioselective aldol reactions of silyl ketene acetals with a variety of aldehydes were achieved by using chiral boranes prepared from the sulfonamides of α-amino acids.