61045-33-8Relevant articles and documents
Novel tartrate-derived guanidine-catalyzed highly enantio- and diastereoselective Michael addition of 3-substituted oxindoles to nitroolefins
Zou, Liwei,Bao, Xiaoze,Ma, Yuanyuan,Song, Yuming,Qu, Jingping,Wang, Baomin
supporting information, p. 5760 - 5762 (2014/05/20)
The Michael addition of 3-substituted oxindoles to nitroolefins was catalyzed by a novel tartrate-derived guanidine in high yield with excellent diastereo- and enantioselectivity. This method showed an extraordinarily broad substrate scope in terms of both reaction partners. the Partner Organisations 2014.
Stereoselective total synthesis of synparvolide B and epi-synparvolide A
Srihari,Vijaya Bhasker,Bal Reddy,Yadav
scheme or table, p. 2420 - 2424 (2009/08/07)
Stereoselective total synthesis of synparvolide B and epi-synparvolide A has been achieved following a convergent approach. Noyori asymmetric Transfer Hydrogenation of ketone and Wadsworth-Emmons olefination reaction are the key steps involved.
Synthesis of 1-Deoxy-D-galactohomonojirimycin via Enantiomerically Pure Allenylstannanes
Achmatowicz, Michal,Hegedus, Louis S.
, p. 2229 - 2234 (2007/10/03)
1-Deoxy-D-galactohomonojirimycin was synthesized in seven steps from optically pure allenylstannane 4 and L-lactate-derived aldehyde 5 in 48% overall yield. The key step was the Lewis acid catalyzed reaction of 4 and 5 to give the syn-amino alcohol in exc