Diastereoselective Synthesis of Piperazines by Manganese-Mediated Reductive Cyclization
作者:Gregory J. Mercer、Matthew S. Sigman
DOI:10.1021/ol034469l
日期:2003.5.1
A simple and effective synthesis of trans aryl-substituted piperazines using a Bronsted acid and manganese(0) is described. [reaction: see text]
描述了一种使用布朗斯台德酸和锰(0)的简单有效的合成反式芳基取代的哌嗪的方法。[反应:看文字]
Selective Monoderivatization of Propane-1,3-diamine with Acid Chlorides: ?Hexahydropyrimidine method?vs. statistic methods
作者:Christian Jentgens、Stefan Bienz、Manfred Hesse
DOI:10.1002/hlca.19970800410
日期:1997.6.30
The selective N-monoderivatization of propane-1,3-diamine (5) with carbonyl and sulfonyl chlorides via2-phenylhexahydropyrimidine (6) was compared with the direct statisticmonoderivatization. It was found that, under optimized conditions, both methods are competitive to one another, depending, however, strongly on the reactivity of the eleclrophile used. The ‘hexahydropyrimidinemethod’ is more reliable
Late transition metal catalysts for olefin polymerization and oligomerization
申请人:Cherkasov Kuzunich Vladimir
公开号:US20060047094A1
公开(公告)日:2006-03-02
This invention relates to a transition metal compound represented by the formula LMX wherein M is a Group 3 to 11 metal L is a bulky bidentate or tridentate neutral ligand that is bonded to M by two or three heteroatoms and at least one heteroatom is nitrogen; X is a substituted or unsubstituted catecholate ligand provided that the substituted catecholate ligand does not contain a 1,2-diketone functionality.
Niitsu, Masaru; Samejima, Keijiro, Chemical and pharmaceutical bulletin, 1986, vol. 34, # 3, p. 1032 - 1038
作者:Niitsu, Masaru、Samejima, Keijiro
DOI:——
日期:——
Electroorganic chemistry. 129. Electroreductive synthesis of chiral piperazines and enantioselective addition of diethylzinc to aldehydes in the presence of the chiral piperazines
Electroreduction of diimines, prepared from 1,2-diamines and aromatic aldehydes, in acidic media gave intramolecularly coupled products, 2,3-diarylpiperazines, stereoselectively. Chiral tri- and tetrasubstituted piperazines were synthesized effectively from chiral 1,2-diamines by the same electroreductive method. Chiral piperazines, prepared from 1(R),2(R)-diaminocyclohexane were effective chiral ligands of catalysts for the enantioselective addition of diethylzinc to aldehydes.