Cycloaddition of pyridine N-imine with 6-alkyl-4-oxohex-5-ynoates followed by condensation with hydrazine provides concise access to pharmacologically active 6-(pyrazolo[1,5-a]pyridin-3-yl)pyridazinones. For the first time alkynyl heterocycles are also shown to be effective dipolarophiles for pyridine N-imine, and analogous compounds can be accessed directly in modest yields through the reactio...

crystal. a) Preparation of porous network complex [(ZnI2)3(1)2(2a)]n. b) Single-crystal-to-single-crystal transformation of 2a into labile imine 3a in the pore of the network complex. c) Crystal structures before and after crystalline-state reaction. NW2/2006G284 Direct Observation of the Labile Imine Formation through Single-crystal-tosingle-crystal Reactions in the Pores of a Porous Coordinat...

In the title compound, C(15)H(15)NO(2), the phenol group make dihedral angles of 2.4 (2) and 24.1 (9)° with the imine linkage (-C=N-) and the phenyl group, respectively, and the mol-ecule adopts the enol-imine tautomeric form, so the mol-ecular structure is stabilized by a strong intra-molecular O-H⋯N hydrogen bond. The crystal structure features a weak C-H⋯π inter-action.

The title compound, C(33)H(30)N(2), has an E configuration at the imine double bond. The angle between the least-squares planes of the imine C=N-C group and the benzene ring of the 2,4,6-trimethylphenyl substituent is 85.38 (11)°. The crystal structure is sustained mainly by inter-molecular π-π inter-actions (3.510 Å) between the two fluorene rings and some C-H⋯π inter-actions.

The reaction of copper(II) chloride and zinc(II) chloride with N-(2-methylphenyl)-3-(1'-salicylaldehydene-2'-imine-ethane)-butanamide(H2L2a) or (MPSB), N-(2-methylphenyl)-3-(1'-(3'-methoxysalicylaldehydene-2'-imine-ethane)-butanamide (H2L2b) or (MPMSB) and N-(2-methylphenyl)-3-(1'-(2'-hydroxyacetylene-2'-imine-ethane)-butanamide (H2L2c) (MPHB) leads to the formation of a series of new complexes...

Racemic boronate-imine and boronate-amine complexes 8 and 10, both featuring a stereogenic boron atom were synthesized from 2-amino-1,1-diphenylethanol (5) and characterized by crystal structure analyses. Proof of enantiomerism at the boron center for the novel boronate-amine complex 10 was established by separation of the enantiomers. Racemization barriers were found to be in the same range fo...

The active site of the aziridination catalyst derived from either the VANOL or VAPOL ligand and B(OPh)(3) is larger than expected and can accommodate not only significant substitution on the diarylmethyl unit of the imine but also that alkyl (but not perfluorylalkyl) substituents on the aryl groups lead to enhanced rates and enantioselection. The screen of diarylmethyl N-substituents on the imi...

the catalytic highly regio-, diastereo-, and enantioselective synthesis of a small library of spiropyrrolizidineoxindolesvia a four-component 1,3-dipolar cycloaddition reaction of azomethine ylides, derived from isatin, with electron-deficient dipolarophilewas described. the process occurs at room temperature in aqueous ethanol as a green solvent and in the presence of a bidendatebis(imine)–cu(...

In this report we present a study of a series of Re(CO)3 pyridine-imine complexes with pendant phenol groups. We investigated the effects of the position of the phenol hydroxyl group (para, meta or ortho to the imine) on the steric and electronic characteristics of a series of Re(CO)3X(pyca-C6H4OH) compounds, where X = Cl, Br and pyca = pyridine-2-carbaldehyde imine. These compounds can be gene...