65559-25-3Relevant academic research and scientific papers
Palladium-Catalyzed Addition of Arylboronic Acids to para- Quinone Methides for Preparation of Diarylacetates
Zhuge, Ruijing,Wu, Liang,Quan, Mao,Butt, Nicholas,Yang, Guoqiang,Zhang, Wanbin
supporting information, p. 1028 - 1036 (2017/03/27)
A palladium-catalyzed addition of arylboronic acids to para-quinone methides has been developed. The catalytic system employing 4,4′-dimethoxy-2,2′-bipyridine (DMeO-BPy) as ligand and trifluoroethanol (TFE) as solvent provides diarylacetate products in high yields. A wide range of functionalized arylboronic acids can be used and the method tolerates some variation in the scope of the para-quinone methides. (Figure presented.).
Inhibitors of lipoprotein(a) assembly
Sexton, Karen E.,Lee, Helen T.,Massa, Mark,Padia, Janak,Patt, William C.,Liao, Peggy,Pontrello, Jason K.,Roth, Bruce D.,Spahr, Mark A.,Ramharack, Randy
, p. 4827 - 4845 (2007/10/03)
Compounds of the general structure A and B were investigated for their activity as lipoprotein(a), [Lp(a)], assembly (coupling) inhibitors. SAR around the amino acid derivatives (structure A) gave compound 14-6 as a potent coupling inhibitor. Oral dosing
Easy large scale syntheses of 2,6-di-t-butyl7-cyano-, 7-carboxy- and 7- methoxycarbonyl quinone methides
Nesvadba, Peter
, p. 2825 - 2832 (2007/10/03)
Easy large scale syntheses of 2,6-di-t-butyl-7-cyano-, 7-carboxy- and 7- methoxycarbonyl quinone methides 1-3 using cheap and readily available starting materials have been developed.
7-substituted quinone methides as inhibitors for unsaturated monomers
-
, (2008/06/13)
Ethylenically unsaturated monomers are protected from premature polymerization during manufacture and storage by the incorporation therein of an effective stabilizing amount of a 7-substituted quinone methide compound.
