A multicomponent reaction of 1,3-dicarbonyls with 1,2-diamines and aromatic aldehydes is described for the direct stereoselective synthesis of 1,4-diazepane derivatives. Various reaction conditions were tested, including an efficient, user-friendly solvent- and catalyst-free procedure.

in this research work, we report the synthesis of macrocyclic diamides from the reaction of diesters and aliphatic diamines in the presence of caesium carbonate. it has been demonstrated that among the carbonate of alkali metals (li2co3, na2co3, k2co3 and cs2co3), cs2co3 appear to be the best catalyst for macrocyclization. diesters with different substitution patterns on the aromatic ring react...

1,2-Diketones have been reacted in one-pot method with 1,2-diamines at room temperature with ZnO nanoparticles as a catalyst. ZnO nanoparticles as an available and reusable catalyst is used for the synthesis of Quinoxalinein improved yields.

Ornithine decarboxylase (ODC) activity of Ehrlich carcinoma cells was increased more than 36-fold after being maintained for 3.5 hr in vitro in a special chamber which allowed continuous perifusion with 0.5 mM ornithine; if incubated in vitro without perifusion the ODC activity was, of course, only 9-fold by the same concentration of ornithine. Ornithine withdrawal from the perifusion medium re...

O-Functionalised salen ligands were employed as bridging ligands in the synthesis of homo- and heterometallic salen complexes with early and late transition metals (H(2)salen: N,N'-bis(salicylidene)ethylenediamine, systematic name: 2,2'-{ethane-1,2-diylbis(nitrilomethylidine)}diphenol). A new type of O-functionalised salen ligand was synthesised, which contains alkyl groups to enhance the solub...

DNA ligases are important enzymes which catalyze the joining of nicks between adjacent bases of double-stranded DNA. NAD+-dependent DNA ligases (LigA) are essential in bacteria and are absent in humans. They have therefore been identified as novel, validated and attractive drug targets. Using virtual screening against an in-house database of compounds and our recently determined crystal structu...

Some Copper(II)-Manganese(II) trinuclear complexes of Schiff bases derived from 2aminobenzaldehyde and diamines are reported and characterized based on their elemental analyses, conductivity studies, IR, UV-Visible, ESR spectroscopy and cyclic voltammetric studies. The complexes are found to have the formula [Mn(CuL)2](CH3COO)2. The elemental analyses data confirms the formation of trinuclear c...

The reaction of 6-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione (1) as a binucleophile with primary aromatic or heterocyclic amines and formaldehyde or aromatic (heterocyclic) aldehydes in a molar ratio (1:1:2) gave the pyrimido[4,5-d]pyrimidin-2,4-dione ring systems 2-5. Treatment of 1 with diamines and formalin in molar ratio (2:1:4) gave the bis-pyrimido[4,5-d]pyrimidin-2,4-diones 6-8. Furth...

An asymmetric ring-opening reaction of meso-aziridines with TMSN3 was developed using a catalyst prepared from Y(OiPr)3 and chiral ligand 2 in a 1:2 ratio. Excellent enantioselectivity was realized from a wide range of substrates with a practical catalyst loading. The products were efficiently converted to enantiomerically enriched 1,2-diamines, which are versatile chiral building blocks for ph...