54763-67-6Relevant academic research and scientific papers
Asymmetric phase transfer Darzens reactions catalyzed by d-glucose- and d-mannose-based chiral crown ethers
Rapi, Zsolt,Bako, Peter,Keglevich, Gyoergy,Szoellsy, Aron,Drahos, Laszlo,Botyanszki, Adrienn,Holczbauer, Tamas
experimental part, p. 489 - 496 (2012/07/28)
Liquid-liquid phase asymmetric Darzens condensations were carried out in the presence of d-glucose- and d-mannose-based crown ethers 1 and 2 as the catalyst. The use of d-glucose-based lariat ether 1 as the catalyst gave the best results. The reaction of
Stereoselective Epoxidation of 2-Arylidene-1-indanones and 2-Arylidene-1-benzosuberones
Adam, W.,Halasz, J.,Jambor, Z.,Levai, A.,Nemes, C.,et al.
, p. 683 - 690 (2007/10/03)
Oxidation of the (E) and (Z) isomers of 2-arylidene-1-indanones (1) and 2-arylidene-1-benzosuberones (4) by alkaline hydrogen peroxide (method i) afforded the spiroepoxides trans-2a-g and trans-5a-g from both isomers as sole products in high yields.On the
Substituted indeno, naphtho and cyclohepta pyrazoles
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, (2008/06/13)
Substituted indeno [1,2-c] pyrazoles, naphtho [1,2-c] pyrazoles and benzo [6,7] cyclohepta [1,2-c] pyrazoles e.g., 3-(2,3-dimethoxyphenyl)-4H-indeno[1,2-c] pyrazole and 4,5-dihydro-3-(4-pyridyl)-2H-naphtho[1,2-c] pyrazole, are useful as non-estrogenic anti-fertility agents and antihypertensive agents.
