132345-13-2Relevant academic research and scientific papers
Asymmetric Diels-Alder Reaction of Optically Active α-(2-exo-Hydroxy-10-bornyl)sulfinylmaleimides and its Application to Optically Active 5-Functionalised Pyrrolines via Retro-Diels-Alder Reaction
Arai, Yoshitsugu,Matsui, Makoto,Fujii, Akihito,Kontani, Tohru,Ohno, Toshiyuki,et al.
, p. 25 - 40 (2007/10/02)
Optically pure sulfinylmaleimides 1 have been synthesized.The Diels-Alder reactions of the sulfoxides 1 with various dienes showed high diastereoselectivity.Regioselective reduction of the adducts 4c and 6c followed by desulfination afforded the γ-hydroxy
Powerful Dienophiles for Asymmetric Diels-Alder Reactions: α-(2-exo-Hydroxy-10-bornylsulfinyl)maleimides
Arai, Yoshitsugu,Matsui, Makoto,Koizumi, Toru,Shiro, Motoo
, p. 1983 - 1985 (2007/10/02)
Enantiomerically pure N-substituted α-(2-exo-hydroxy-10-bornylsulfinyl)maleimides 1 have been synthesized diastereoselectively, and these dienophiles undergo Diels-Alder reactions readily with furan to give the corresponding cycloadducts with high diastereoselectivity.
