15212-29-0

Upstream product

• 2579-22-8 Phenylpropargyl aldehyde 
• 27720-98-5 isobutylmagnesium iodide 
• 2170-06-1 1-Phenyl-2-(trimethylsilyl)acetylene 
• 590-86-3 isovaleraldehyde 
• 1004-22-4 (phenylethynyl)sodium 
• 1407998-85-9 2-(5-methyl-1-phenylhex-1-yn-3-yl)isoindoline-1,3-dione 
• 4440-01-1 lithium phenylacetylide 

Downstream Products

• 23566-47-4 5-methyl-1-phenyl-hex-1-yn-3-one 
• 15175-34-5 (E)-5-methyl-1-phenyl-hex-2-en-1-one 
• 1174667-69-6 C₁₆H₂₀O₃ 
• 1346155-61-0 1-isobutyl-1H-inden-3-yl benzoate 
• 1346155-33-6 5-methyl-1-phenylhex-1-yn-3-yl benzoate 
• 1407998-85-9 2-(5-methyl-1-phenylhex-1-yn-3-yl)isoindoline-1,3-dione 
• 872309-99-4 5-methyl-1-phenylhexan-3-ol 

Relevant academic research and scientific papers

Kinetic resolution of propargylamines via a highly enantioselective non-enzymatic N-acylation process

The non-enzymatic kinetic resolution of diversely substituted primary propargylic amines is reported featuring a highly selective acetyl transfer using (1S,2S)-1 in conjunction with AliquatTM 336, affording the corresponding enantio-enriched N-

Regio- and stereoselective formation of conjugated dienes by titanocene(ii)-promoted alkylation of propargyl carbonates

Conjugated dienes were produced with complete regio- and stereoselectivity by the titanocene(ii)-promoted alkylation of propargyl carbonates via the formation of 2,3,4-trisubstituted titanacyclobutenes.