120641-24-9

Upstream product

• 120615-59-0 di-l-menthyl methylenemalonate 
• 73636-64-3 Malonsaeure-bis<(1R)-menthyl>ester 
• 15356-60-2 (1S,2R,5S)-(+)-menthol 
• 120615-60-3 di-l-menthyl bicyclo<2.2.1>hept-5-ene-2,2-dicarboxylate 
• 133188-11-1 Di-l-menthyl (1S)-1,3-dithietan-2-ylidenemalonate 1-oxide 
• 133188-14-4 Di-l-menthyl 1,3-dithietan-2-ylidenemalonate 
• 73636-64-3 di-l-menthyl malonate 
• 133188-13-3 C₃₀H₄₆O₅S₂ 

Relevant academic research and scientific papers

Titanium Tetrachloride-Mediated Diels-Alder Reactions of Cyclopentadiene with Di-l-menthyl Methylenemalonate and Its Acetoxy Derivative as New Chiral Dienophiles for Asymmetric Induction

Asymmetric synthesis of -2,3-dihydroxy-4-hydroxymethylcyclopent-1ylmalonate (its racemic form is already known as a versatile building block for carbocyclic C-nucleosides) was achieved by Diels-Alder reaction of cyclopentadiene with di-l-ment