111998-78-8Relevant academic research and scientific papers
Di-l-menthyl (Acetoxymethylene)malonate, a New Chiral Dienophile: Enantioselective Route to Carbocyclic Analogues of C-Nucleoside
Katagiri, Nobuya,Haneda, Toru,Hayasaka, Etsuko,Watanabe, Nobuhisa,Kaneko, Chikara
, p. 226 - 227 (2007/10/02)
Titanium tetrachloride promoted Diels-Alder reaction of new chiral dienophile, di-l-menthyl (acetoxymethylene)malonate, with cyclopentadiene not only proceeds with high diastereofacial selectivity but also provides an efficient enantioselective synthetic
