1215086-63-7

Upstream product

• 1120-72-5 2-Methylcyclopentanone 
• 309756-60-3 E/Z-2-(RS)-N-[(R)-1-phenylethyl]-2-methylcyclopentylideneamine 
• 184759-43-1 3-((S)-1-Methyl-2-oxo-cyclopentyl)-propionic acid methyl ester 
• 1215086-73-9 C₁₁H₂₀O₃ 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant academic research and scientific papers

Intramolecular reductive ketone-alkynoate coupling reaction promoted by (η2-propene)titanium

Intramolecular reductive coupling of cycloalkanones tethered to alkynoates in the presence of (η2-propene)titanium was successfully performed to provide hydroxy-esters in a diastereoselective manner. Subsequent lactonization afforded angularly

Synthesis of racemic and enantiomerically pure acetylenic -keto esters derived from 2-methyl-1,3-cycloalkanediones and 2-methylcycloalkanones respectively

Racemic and enantiomerically pure alkynyl esters tethered, respectively, to 2-methyl-1,3-cycloalkanediones and 2-methylcycloalkanones were readily obtained starting from common intermediates, which were available on large scale.