1190109-48-8Relevant academic research and scientific papers
Organocatalyzed Enantioselective Allylation of Isatins by Using a Chiral Amino Alcohol Derived Squaramide as Catalyst
Ghosh, Debashis,Gupta, Naveen,Abdi, Sayed H.R.,Nandi, Sekhar,Khan, Noor-Ul H.,Kureshy, Rukhsana I.,Bajaj, Hari C.
, p. 2801 - 2806 (2015/05/04)
A series of new squaramide-based organocatalysts were synthesized from commercially available 3,4-dimethoxycyclobut-3-ene-1,2-dione in two steps. A 2.5 mol-% loading of the organocatalyst successfully catalyzed the asymmetric allylation of isatins with al
Chiral CNN pincer palladium(II) complexes with 2-aryl-6-(oxazolinyl) pyridine ligands: Synthesis, characterization, and application to enantioselective allylation of isatins and suzuki-miyaura coupling reaction
Wang, Tao,Hao, Xin-Qi,Huang, Juan-Juan,Wang, Kai,Gong, Jun-Fang,Song, Mao-Ping
, p. 194 - 205 (2014/02/14)
A series of chiral 2-aryl-6-(oxazolinyl)pyridine (aryl = phenyl or 1-naphthyl) ligands 2a-f were conveniently prepared from commercially available 6-bromo-2-picolinaldehyde in two steps. Reaction of 2a-f with PdCl2 in toluene in the presence of
SIMPLE ORGANIC MOLECULES AS CATALYSTS FOR PRACTICAL AND EFFICIENT ENANTIOSELECTIVE SYNTHESIS OF AMINES AND ALCOHOLS
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Paragraph 00193; 00194; 00195; 00301, (2013/09/12)
The present invention provides organic molecules and methods thereof for reactions between organoboron reagents and double bonds, such as imines or carbonyls, to stereoselectively provide chiral products including amines and alcohols, entities useful for
