1228293-95-5

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 1374348-46-5 (S,E)-1-((R)-4-benzyl-2-thioxothiazolidin-3-yl)-3-(tert-butyldimethylsilyloxy)-5-phenylpent-4-en-1-one 
• 1374348-43-2 (S,E)-1-((R)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-5-phenylpent-4-en-1-one 
• 1228293-94-4 C₁₈H₂₈OSi 

Downstream Products

• 1228293-93-3 C₂₀H₃₂O₂Si 
• 91327-34-3 (R)-6-((S,E)-2-hydroxy-4-phenylbut-3-en-1-yl)-5,6-dihydro-2H-pyran-2-one 
• 1374348-52-3 C₁₉H₃₀O₃Si 
• 1374348-41-0 methyl (2Z,5R,7S,8E)-7-(tert-butyldimethylsilyloxy)-5-hydroxy-9-phenylnona-2,8-dienoate 
• 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

A concise total synthesis of (+)-neopeltolide

(Figure Presented) Short and sweet: The highly potent antiproliferative marine macrolide (+)-neopeltolide has been synthesized based on the strategic application of olefin metathesis reactions. The total synthesis proceeded in only 13 steps from commercially available starting materials, and represents the shortest synthesis of (+)-neopeltolide reported to date.