126863-91-0

Upstream product

• 106-54-7 p-Chlorothiophenol 
• 16260-59-6 1,6-dichlorohexa-2,4-diyne 
• 126863-90-9 1-chloro-6-(4'-chlorobenzenethio)-2,4-hexadiyne 

Downstream Products

• 126863-94-3 1,2-Dichloro-4-[(Z)-1-(4-chloro-benzenesulfonylmethyl)-pent-1-en-3-ynylsulfanyl]-benzene 
• 126863-88-5 1,2-Dichloro-4-[(E)-1-(4-chloro-benzenesulfonylmethyl)-pent-1-en-3-ynylsulfanyl]-benzene 
• 126863-92-1 C₁₈H₁₄BrClO₂S₂ 
• 126884-25-1 C₁₈H₁₄BrClO₂S₂ 
• 126863-87-4 C₁₈H₁₄Cl₂O₂S₂ 
• 126863-89-6 4-[(E)-1-(4-Chloro-benzenesulfonylmethyl)-pent-1-en-3-ynyl]-morpholine 
• 126863-86-3 1-(4'-chlorobenzensulfonyl)-2,4-hexadiyne 

Relevant academic research and scientific papers

CONTROL OF REGIOCHEMISTRY, STEREOCHEMISTRY AND STOICHIOMETRY IN ADDITIONS TO ALKADIYNES. SYNTHETIC VALUE OF A SULFONE FUNCTION.

The strategic placement of a sulfone function alpha to a conjugated alkadiyne is shown to enforce total control of regiochemistry, stereochemistry and stoichiometry in additions of nucleophiles across the triple bonds.