918798-99-9Relevant academic research and scientific papers
Synthesis of Yb complexes with amino-acid-armed ligands for direct asymmetric tandem aldol reduction reactions
Stodulski, Maciej,Jazwinski, Jaroslaw,Mlynarski, Jacek
, p. 5553 - 5562 (2008)
A synthetic route to a series of C2-symmetric chiral ligands armed with selectively protected amino acids have been developed with the aim to study the potential of the corresponding Yb(III) complexes for enantioselective direct aldol reactions
Efficient preparation of 1,3-Diol derivatives with three contiguous stereocenters by an enantioselective direct aldol-tishchenko reaction
Ichibakase, Tomonori,Nakajima, Makoto
, p. 3145 - 3151 (2012/11/13)
1,3-Diol derivatives with three contiguous stereocenters were efficiently prepared by an enantioselective direct aldol-Tishchenko reaction catalyzed by dilithium 3,3-diphenylbinaphtholate. The reactions of acyclic ketones as aldol donors gave 1,2-syn-1,3-
Direct enantioselective aldol-tishchenko reaction catalyzed by chiral lithium diphenylbinaphtholate
Ichibakase, Tomonori,Nakajima, Makoto
supporting information; experimental part, p. 1579 - 1581 (2011/05/03)
Chiral lithium diphenylbinaphtholate is an effective catalyst for the enantioselective aldol-Tishchenko reaction, affording 1,3-diol derivatives with three contiguous chiral centers and high stereoselectivities. Successive aldol-aldol-Tishchenko reactions
