88842-06-2

Upstream product

• 88853-99-0 (2R,3R)-2-Methoxy-5-phenyl-1-(tetrahydro-pyran-2-yloxy)-pentan-3-ol 
• 88842-14-2 (2S,3S)-5-Phenyl-1-(tetrahydro-pyran-2-yloxy)-pentane-2,3-diol 
• 344889-76-5 2-((E)-5-Phenyl-pent-2-enyloxy)-tetrahydro-pyran 
• 55282-95-6 ethyl (2E)-5-phenylpent-2-enoate 
• 75553-23-0 (E)-5-phenyl-2-penten-1-ol 
• 88842-05-1 2-Methoxy-5-phenyl-1,3-pentanediol 
• 98-59-9 p-toluenesulfonyl chloride 
• 88853-99-0 (2R,3S)-2-Methoxy-5-phenyl-1-(tetrahydro-pyran-2-yloxy)-pentan-3-ol 
• 88842-14-2 (2S,3R)-5-Phenyl-1-(tetrahydro-pyran-2-yloxy)-pentane-2,3-diol 
• 344889-82-3 2-((Z)-5-Phenyl-pent-2-enyloxy)-tetrahydro-pyran 
• 88842-13-1 (Z-)-ethyl 5-phenylpent-2-enoate 
• 39520-63-3 (Z)-5-phenylpent-2-en-1-ol 

Downstream Products

• 74824-85-4 (2S,3R)-3-Methoxy-2-phenethyl-oxetane 
• 74824-84-3 cis-3-Methoxy-2-(2-phenylethyl)oxetane 

Relevant academic research and scientific papers

Reactions of 3-Hydroxyvinyl Selenones with Alkoxides. Oxetane Formation and Fragmentation Reactions

3-Hydroxyvinyl phenyl selenones are prepared and their behavior as conjugate addition acceptors has been investigated.As a result, a selenonyl group has been found to activate the C=C bond for conjugate addition of nucleophiles and further to behave as an