175410-69-2

Upstream product

• 2579-22-8 Phenylpropargyl aldehyde 
• 110-87-2 3,4-dihydro-2H-pyran 
• 175410-79-4 rac-ethyl 3-hydroxy-5-phenylpent-4-ynoate 

Downstream Products

• 175410-81-8 Toluene-4-sulfonic acid 5-phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-4-ynyl ester 
• 175410-70-5 dl-1-phenyl-5-(p-toluenesulfonyloxy)-1-pentyn-3-ol 
• 41415-69-4 (dl)-2-(2-phenylethynyl)oxetane 
• 175410-80-7 5-Phenyl-3-(tetrahydro-pyran-2-yloxy)-pent-4-yn-1-ol 

Relevant academic research and scientific papers

Synthesis of alkylidenecyclopentenones and dialkylidenecyclopentenones via the coupling of propargylic alcohol and 2-alkyne-1,4-diol derivatives with cyclopropylcarbene-chromium complexes

The coupling of propargylic alcohols and their derivatives with cyclopropylcarbene-chromium complexes has been investigated. The coupling reaction leads to alkylidenecyclopentenones or alkoxyalkyl-cyclopentenones, depending on the leaving group ability of

Synthesis of alkylidenecyclopentenones via the coupling of propargyl alcohol derivatives with cyclopropylcarbene-chromium complexes

(equatio presented) The coupling of propargylic alcohols and their derivatives with cyclopropylcarbene-chromium complexes has been investigated. The coupling reaction leads to alkylidenecyclopentenones or alkoxyalkylcyclopentenones, depending on the leavi

Chiral bipyrindine and biquinoline ligands: Their asymmetric synthesis and application to the synthesis of trans-whisky lactone

Chiral bipyrindine and biquinoline which have been reported to be efficient ligands for the construction of chiral copper catalysts, were synthesized enantioselectively by using Mn-salen catalyzed asymmetric epoxidation as a key step. Enantioselective synthesis of trans-whisky lactone was then achieved by way of enantiospecific ring expansion reaction of oxetane with a chiral copper catalysts bearing the bipyrindine ligand as a chiral source.