The non-symmetric title mol-ecule, C32H34N2O5, is based on a tetra-substituted ethyl-enedi-amine backbone. The mol-ecular structure consists of three hy-droxy-benzyl groups and one 2-hy-droxy-5-methyl-benzaldehyde group bonded to the N atoms of the di-amine unit. The ethyl-enedi-amine skeleton shows a regular extended conformation, while the spatial orientation of the phenol arms is governed by...

The title compound, C(17)H(18)N(2)O(3), is approximately planar, owing in part to an intra-molecular bifurcated O-H⋯(N,O) hydrogen bond; the dihedral angle between the two aromatic rings is 23.86 (9)°. In the crystal struture, centrosymmetrically related mol-ecules associate into dimers via the eight-membered carboxyl-ate {⋯H-O-C=O}(2) synthon.

In the title compound, C(12)H(15)N(3)O(5)S, an intra-molecular N-H⋯O hydrogen bond between the hydrazine unit and one of the carbonyl groups may influence the mol-ecular conformation. In the crystal structure, inter-molecular N-H⋯O hydrogen bonds, including one which is bifurcated, link the mol-ecules into a two-dimensional network.

Macrocycles are commonly synthesized via late-stage macrolactamization and macrolactonization. Strategies involving C–C bond macrocyclization have been reported, examples include the transition-metal-catalyzed ring-closing metathesis coupling reactions. In this mini-review, we summarize recent progress in direct synthesis of polyketide polypeptide macrocycles using a C–H activation strategy. fi...

In t the title compound, C(14)H(12)BrN(3)O(2). H(2)O, the conformation of the C=N double bond in the hydrazide Schiff base mol-ecule is E. The dihedral angle between the benzene rings is 48.01 (11) °. An intra-molecular O-H⋯N hydrogen bond makes an S(6) ring motif. In the crystal, mol-ecules are linked through N-H⋯O (bifurcated acceptor) and O-H⋯O hydrogen bonds, forming two-dimensional network...

The main mol-ecule of the title methanol solvate, C(16)H(10)Cl(2)N(2)O·CH(3)OH, exists in the keto form and the C=O and N-H bonds are mutually cis in the crystal structure. The dihedral angle between the quinoline and benzene rings is 11.17 (3)°. A bifurcated intra-molecular N-H⋯(O,N) hydrogen bond is present as well as an O-H⋯O hydrogen bond. In the crystal, C-H⋯O inter-actions link the 3,5-di...

A novel platinum-mediated process involving intermolecular activation of a C(aryl)-H bond of toluene, intramolecular activation of an imine C(aryl)-Cl bond and formation of a C-C bond is reported.

Herein we report the intramolecular arene C-H and C-F bond oxygenation by tetranuclear iron complexes. Treatment of [LFe3(PhPz)3OFe][OTf]2 (1) or its fluorinated analog [LFe3(F2ArPz)3OFe][OTf]2 (5) with iodosobenzene results in the regioselective hydroxylation of a bridging pyrazolate ligand, converting a C-H or C-F bond into a C-O bond. The observed reactivity suggests the formation of termina...

In the title mol-ecule, C(16)H(15)ClO(4)S, the chloro-thio-phene and trimeth-oxy-phenyl rings make a dihedral angle of 31.12 (5)°. The C=C double bond exhibits an E conformation. In the crystal, C-H⋯O inter-actions generate bifurcated bonds, linking the mol-ecules into chains along the b axis.

In the title compound, C(25)H(24)N(2)O(2), the dihedral angle between the two benzene rings of the benzophenone moiety is 59.10 (6)°. An intra-molecular, bifurcated N-H⋯(O,N) hydrogen bond, which generates S(6) and S(5) rings, respectively, helps to establish the overall conformation of the mol-ecule.