87035-66-3Relevant academic research and scientific papers
Guanidine catalyzed aerobic reduction: A selective aerobic hydrogenation of olefins using aqueous hydrazine
Lamani, Manjunath,Guralamata, Ravikumara Siddappa,Prabhu, Kandikere Ramaiah
supporting information; experimental part, p. 6583 - 6585 (2012/07/14)
An efficient aerobic reduction of olefins, internal as well as terminal, is developed using guanidine as an organocatalyst. A remarkable chemoselectivity in reduction has been demonstrated in the presence of a variety of functional groups and protective groups and a selective reduction of a terminal olefin in the presence of an internal olefin is revealed.
Synthesis and helical properties of aromatic multilayered oligoureas
Kudo, Mayumi,Katagiri, Kosuke,Azumaya, Isao,Kagechika, Hiroyuki,Tanatani, Aya
experimental part, p. 4455 - 4463 (2012/08/13)
Several aromatic multilayered oligoureas with different chain lengths and different numbers of chiral N-substituents were synthesized, and their helical conformation and induced handedness were examined by means of CD spectroscopy. Introduction of one chi
Copper catalyzed coupling of aryl chlorides, bromides and iodides with amines and amides
Xu, Hanhui,Wolf, Christian
supporting information; experimental part, p. 1715 - 1717 (2009/08/08)
A copper(i) catalyzed procedure for carbon-nitrogen bond formation utilizing aryl halides and either amines, including amino acids and diphenylamine, or aliphatic and aromatic amides is described. The Royal Society of Chemistry.
Reductive N-monoalkylation of primary aromatic amines
Verardo,Giumanini,Strazzolini,Poiana
, p. 121 - 125 (2007/10/02)
Primary aromatic amines 1 with a variety of ring substituents are easily converted to their N-monoalkyl derivatives 3 by a simple variation of the sodium borohydride/sulfuric acid/carbonyl compound procedure previously described for their N-permethylations. The procedure is suitable for the α-minodeuterium labelling of the new N-substituent.
