80900-32-9Relevant academic research and scientific papers
Regioselective Access to 3-Aryl-1-aminoisoquinolines via Nickel(I)-Catalyzed C-C and C-N Cascade Coupling Reactions from the Substituted 2-(Cyanomethyl)benzonitriles
Yang, Xicheng,Yu, Haihua,Xu, Yulong,Shao, Liming
, p. 9682 - 9695 (2018/09/06)
A novel and regioselective Ni(I) catalyzed C-C and C-N cascade coupling reactions has been developed. The cascade furnishes atom-economic access to 40 3-aryl-1-aminoisoquinolines. The regioselectivity of C(sp3)-cyano group over C(sp2
HETEROCYCLIC COMPOUND
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Paragraph 1109, (2016/03/18)
The present invention provides a heterocyclic compound having an RORγt inhibitory action. The present invention relates to a compound represented by the formula (I): wherein Ar is a the partial structure (1) to the partial structure (5), Q is a bivalent group selected from the group consisting of (Ia)-(If), and B is a ring optinally having substituent(s), or a salt thereof.
OXIDATION OF ALCOHOLS BY TRANSITION METAL COMPLEXES PART V. SELECTIVE CATALYTIC MONOALKYLATION OF ARYLACETONITRILES BY ALCOHOLS
Grigg, Ronald,Mitchell, Thomas R. B.,Sutthivaiyakit, Somyote,Tongpenyai, Ngampong
, p. 4107 - 4110 (2007/10/02)
Selective catalytic monoalkylation of arylacetonitriles by primary alcohols can be achieved at o using a catalyst prepared in situ from rhodium trichloride, triphenylphosphine and sodium carbonate.RuH2(PPh3)4 is a more effective catalyst for this process.
