72450-68-1Relevant academic research and scientific papers
REDUCTION WITH ORGANIC SELENIUM COMPOUNDS II. REDUCTION OF SCHIFF BASES WITH SELENOPHENOL. REDUCTIVE ALKYLATION OF AMINES WITH CARBONYL COMPOUNDS
Fujimori, Ken,Yoshimoto, Hiroshi,Oae, Shiguri
, p. 3385 - 3388 (1980)
Reduction of Schiff bases with selenophenol proceeded at room temperature to yield the corresponding sec. amines quantitatively.The reaction of either prim. amine or sec. amine with carbonyl compounds and selenophenol gave sec. or tert. amines, respectively.Different alkyl groups can be introduced successively on nitrogen of prim. amines to afford tert. amines bearing three different alkyl groups desired by one pot reaction.
Synthesis of unsymmetric tertiary amines via alcohol amination
Pang, Shaofeng,Deng, Youquan,Shi, Feng
supporting information, p. 9471 - 9474 (2015/06/08)
The first one-pot selective synthesis of unsymmetric tertiary amines is reported by the amination of two types of alcohols with primary amines via the development of a simple CuAlOx-HT catalyst and enables the synthesis of unsymmetric amines in a wide variety of primary amines and alcohols.
Cooperative two-photon absorption enhancement by through-space interactions in multichromophoric compounds
Terenziani, Francesca,Parthasarathy, Venkatakrishnan,Pla-Quintana, Anna,Maishal, Tarun,Caminade, Anne-Marie,Majoral, Jean-Pierre,Blanchara-Desce, Mireille
supporting information; experimental part, p. 8691 - 8694 (2010/01/16)
Spaceinvaders:Aseriesofmultichromophores(fromdinnerstodendritic24mers) issynthesized,spectroscopicallycharacterized,andtheoreticallymodeled. Enhancementofthetwo photonabsorptionresponsedependsonthenumberanddistributionofchromophoricsubun its(seepicture,re
