نتایج جستجو برای: quinolines multicomponent reaction molecular iodine

تعداد نتایج: 1036260  

Journal: :journal of nanostructures 2014
s. c. azimi e. abbaspour-gilandeh

a simple and efficient method for the synthesis of quinolines and polycyclic quinolines using li+ modified nanoporous na+-montmorillonite is described. this new nanocatalyst proceeds via friedlander annulation under solvent-free conditions. it describes our observations about a trend of catalytic activity of lithium cation in nanoporous na+-montmorillonite. in this study, several types of 1,3-d...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2016
ghodsi mohammadi ziarani faezeh aleali negar lashgari alireza badiei

one-pot multicomponent reaction between isatin, barbituric acid, and 6-amino-1,3-dimethyl uracil was investigated in the presence of sulfonic acid functionalized nanoporous silica (sba-pr-so3h) and resulted in the formation of spirooxindole dipyrimidines. spirooxindole unit is found in many natural products and biologically active molecules and 1,4-dihydropyridines are an important class of com...

2011
Xin-Yuan Chen Min-Min Zhao Xu Qian Shao-Gang Hou

The title compound, C(22)H(20)N(2)O(2), was synthesized via a multicomponent reaction using naphthalen-2-ol, morpholine and 4-formyl-benzonitrile. The dihedral angle between the naphthalene ring system and the benzene ring is 81.25 (10)°. The morpholine ring adopts a chair conformation. The mol-ecular conformation is stabilized by intra-molecular O-H⋯N and C-H⋯O hydrogen bonds. In the crystal, ...

Journal: :Angewandte Chemie 2013
Dongbing Zhao Frank Glorius

Asymmetric hydrogenation of (hetero)arenes is one of the most straightforward ways to synthesize enantiomerically pure, saturated or partially saturated cyclic molecules. Recent progress has significantly expanded the substrate scope of this reaction. Whereas a number of highly efficient catalytic systems have been found for the asymmetric hydrogenation of quinolines, structurally related isoqu...

Journal: :The Journal of vitaminology 1964
I UTSUMI K HARADA K KOHNO

(1, 2). However, it was reported in the foregoing paper (3), that the -S-Slinkages formed by iodine oxidation of the SH-groups of native egg albumin could react with the thiol-form of thiamine or O-benzoylthiamine (OBT) without denaturation. To investigate the effect of denaturation on the reaction is an interesting problem, giving means of elucidating the molecular structure of pro teins. Inve...

Journal: :The Journal of Experimental Medicine 1962
Donald G. McKay Ting-Chao Wong

By molecular distillation of oxidized cod liver oil a partial isolation of the lipid species responsible for the diet-induced generalized Shwartzman reaction in pregnant rats has been achieved. Molecular distillation produced three fractions and a residue. Qualitative and quantitative differences in each fraction were shown by determining iodine and saponification numbers and by thin layer chro...

Journal: :journal of nanostructures 2013
j. safari z. zarnegar

in this investigation, a facile and green sonochemical route has been developed for the synthesis of 2-ketomethylquinolines by using 2-methylquinolines and several acyl chlorides in the presence of nanocrystalline mgal2o4 as an efficient heterogeneous catalyst. the combination of nanocatalyst and ultrasonic process afforded corresponding ketomethyl quinolines in shorter reaction durations, and ...

Journal: :European Journal of Organic Chemistry 2022

Various isocyanide-based multicomponent reactions prove to be highly reliable when ?-substituted ?-amino boronic esters are employed as the amine component, allowing efficient synthesis of unprecedented peptidomimetics and heteroatom-rich boron-containing small molecules. In particular, scope Ugi reaction is widely exploited, give a family enantiopure ?-amido boronates. The Ugi-azide van Leusen...

Journal: :Chemical & pharmaceutical bulletin 2002
Reiko Fujita Noriyuki Watanabe Hiroshi Tomisawa

2-Alkyl-1-alkylthioisoquinolinium salts were readily prepared from 2-alkyl-1(2H)-isoquinolones via 2-alkyl1(2H)-thioisoquinolones in two steps. Under mild conditions, the reaction of 2-alkyl-1-alkylthioisoquinolinium salts with active methylene compounds in the presence of sodium hydride afforded 2-alkyl-1-(substituted methylene)iso-quinolines in good yields. Pyrrolo[2,1-a]isoquinolines were sy...

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