245366-30-7Relevant academic research and scientific papers
Stereoselective conjugate addition of alkyl groups to (S)-4-(tert-butyldimethylsilyloxy)-2-cyclopentenone derivatives
Yakura, Takayuki,Tanaka, Kenji,Kitano, Tomoko,Uenishi, Jun'Ichi,Ikeda, Masazumi
, p. 7715 - 7721 (2007/10/03)
Reaction of (S)-2-benzenesulfonyl-4-(tert-butyldimethylsilyloxy)-2-cyclopentenone (2) and a 2-methoxycarbonyl congener (3) with R2CuLi or RMgBr-CuI stereoselectively gave (2S,3R,4S)-3-alkyl-2-benzenesulfonyl-4-(tert-butyldimethysilyloxy)cyclopentan one (4) and its (2S,3S,4S)-2-methoxycarbonyl derivative (5) as a major diastereoisomer. On the other hand, reaction with R3Al in toluene exclusively gave the corresponding 3,4-cis-adducts 6 and 7. (C) 2000 Elsevier Science Ltd.
Stereoselective conjugate addition of alkyl groups to (S)-4-(tert- butyldimethylsilyloxy)-2-phenylsulfonyl-2-cyclopentenone by means of trialkylaluminum reagents
Yakura, Takayuki,Tanaka, Kenji,Iwamoto, Miki,Nameki, Masatake,Ikeda, Masazumi
, p. 1313 - 1315 (2007/10/03)
Reaction of (S)-4-(tert-butyldimethylsilyloxy)-2-phenylsulfonyl-2- cyclopentenone with 2.2 stereoselectivity afforded the corresponding (2R,3S,4S)-4-(tert-butyldimethylsilyloxy)-3-alkyl-2-phenylsulfonyl- cyclopentanones as a single diastereoisomer.
