1335013-63-2

Upstream product

• 1335014-32-8 (R,E)-5-(4-methoxybenzyloxy)-1-phenylpent-1-en-3-yl acetate 
• 1335014-38-4 (R,E)-5-hydroxy-1-phenylpent-1-en-3-yl acetate 
• 1335014-92-0 C₁₃H₁₄O₃ 
• 24850-33-7 allyltributylstanane 
• 1335014-12-4 5-(4-methoxybenzyloxy)-1-phenylpent-1-yn-3-ol 
• 1335014-19-1 5-(4-methoxybenzyloxy)-1-phenylpent-1-yn-3-one 
• 1335013-78-9 (3R)-5-[(4-methoxyphenyl)methoxy]-1-phenylpent-1-yn-3-ol 
• 1335014-28-2 (R,E)-5-(4-methoxybenzyloxy)-1-phenylpent-1-en-3-ol 

Downstream Products

• 188054-12-8 (1E,3R,5S,7E)-5-hydroxy-8-((R)-6-oxo-3,6-dihydro-2H-pyran-2-yl)-1-phenylocta-1,7-dien-3-yl acetate 
• 1260145-38-7 (1E,3R,5S)-1-phenylocta-1,7-diene-3,5-diol 
• 1260145-21-8 (4S,6R)-4-allyl-2,2-dimethyl-6-[(E)-2-phenylvinyl]-1,3-dioxane 
• 1355358-01-8 (3R,5S,E)-3-acetoxy-1-phenylocta-1,7-dien-5-yl acrylate 

Relevant academic research and scientific papers

Stereoselective total synthesis of (+)-cryptofolione and (+)-goniothalamin

The stereoselective total synthesis of two naturally occurring α-pyrone derivatives (+)-cryptofolione and (+)-goniothalamin has been accomplished via a common intermediate. The synthetic sequence involves the asymmetric reduction of a propargyl ketone and olefin cross-metathesis as the key reactions.