142467-50-3Relevant academic research and scientific papers
Diastereoselective Diels-Alder Cycloadditions with Chiral 1-(Alkylsulfinyl)-2-nitroalkenes
Fuji, Kaoru,Tanaka, Kiyoshi,Abe, Hitoshi,Matsumoto, Kiyoshi,Harayama, Takashi,et al.
, p. 2211 - 2218 (2007/10/02)
Several chiral 2-nitro-1-sulfinylalkenes were prepared and examined for their utility as dienophiles for asymmetric cycloaddition.Trisubstituted dienophiles 3-6 undergo diastereoselective cycloaddition with cyclopentadiene in the presence of Lewis acids.Even the tetrasubstituted chiral sulfinyl dienophiles 1 and 2 could be coerced into undergoing cycloaddition to afford the cycloadducts in high yield without concomitant elimination if the reaction was conducted under high pressure.Generally, the Z-sulfinyl dienophiles 1-4 showed higher diastereo- and endo/exo-selectivity than the E-dienophiles 5 and 6.
Diastereoselective Diels-Alder reactions with chiral sulfinyl derivatives as dienophiles under high pressure
Fuji,Tanaka,Abe,Matsumoto,Taga,Miwa
, p. 609 - 612 (2007/10/02)
Using the high pressure technique, asymmetric Diels-Alder reaction utilizing chiral 2-nitro-1-sulfinylolefins and dienes proceeded smoothly to give highly functionalized cyclohexene derivatives with satisfactory chemical yield and high diastereomeric exce
