1374348-41-0

Upstream product

• 1374348-42-1 (3S,5S,E)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-5-(tert-butyldimethylsilyloxy)-3-hydroxy-7-phenylhept-6-en-1-one 
• 1374348-46-5 (S,E)-1-((R)-4-benzyl-2-thioxothiazolidin-3-yl)-3-(tert-butyldimethylsilyloxy)-5-phenylpent-4-en-1-one 
• 1374348-52-3 C₁₉H₃₀O₃Si 
• 88738-78-7 bis-(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate 
• 1228293-95-5 C₁₇H₂₆O₂Si 
• 14371-10-9 (E)-3-phenylpropenal 

Downstream Products

• 91327-34-3 (R)-6-((S,E)-2-hydroxy-4-phenylbut-3-en-1-yl)-5,6-dihydro-2H-pyran-2-one 
• 1374348-47-6 (R)-6-((S,E)-2-(tert-butyldimethylsilyloxy)-4-phenylbut-3-enyl)-5,6-dihydro-2H-pyran-2-one 
• 67144-65-4 (S,E)-1-((R)-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