1374348-45-4

Upstream product

• 1374348-43-2 (S,E)-1-((R)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-phenylpent-4-en-1-one 
• 133271-07-5 C₁₁H₁₂O₂ 
• 1374348-48-7 (S,2E,6E)-5-hydroxy-N-methoxy-N-methyl-7-phenylhepta-2,6-dienamide 
• 100-52-7 benzaldehyde 
• 14371-10-9 (E)-3-phenylpropenal 

Downstream Products

• 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 

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