THE DIHEDRAL ANGLE BETWEEN THE PLANES OF TWO AROMATIC RINGS IN THE TITLE COMPOUND [SYSTEMATIC NAME: 3-benzoyl-5-chloro-pyrimidine-2,4(1H,3H)-dione], C(11)H(7)ClN(2)O(3), is 86.79 (6)°. Centrosymmetric dimers formed by N-H⋯O hydrogen bonds are linked through C-H⋯O inter-actions, forming a two-dimensional network parallel to (10).

Cyclopentadienyl ligands are ubiquitous in lanthanide chemistry and have been used extensively to stabilize low-valent lanthanide(II) complexes. We now report the reactions of β-diketiminate ytterbium(II) hydride [(BDIDipp)Yb(H)]2 (BDIDipp = HC{C(Me)NDipp}2, Dipp 2,6-iPr2C6H3) with tetramethylcyclopentadiene, pentamethylcyclopentadiene, indene, fluorene; provide ready access heteroleptic η5-C5R...

In the title compound, C(11)H(14)N(4)O(4)·C(2)HCl(3)O(2), the dioxolane ring adopts an envelope conformation. Doxophylline [7-(1,3-dioxolan-2-yl-meth-yl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione] and trichloro-acetic acid mol-ecules are linked by O-H⋯N and C-H⋯O hydrogen bonds.

Condensation of aromatic primary bis-amines with isatin (1H-indole-2,3-dione) and 5-flouroisatin occurred cleanly and efficiently in a water suspension medium without using any organic solvent or acid catalyst. The corresponding bis-Schiff bases were obtained in good yields and were easily isolated by filtration. Their structures were confirmed by (1)H-NMR, (13)C-NMR, IR and mass spectra.

A series of new azo amino uracil dyes were synthesized by diazotization of nine aromatic amines using sodium nitrite and hydrochloric acid and subsequent coupling to 6-aminopyrimidine-2, 4(1H, 3H) – dione. The effects of solvents, substituents, acid and base on the visible absorption maxima of the dyes were also discussed.

Enyne alcohols can react as precursors of either dienes or dienophiles with different substrates after hydroxylation and isomerization by gold catalysis. As such, oxa-bridged tricyclo[5.2.2.02,6]-undec-8-ene-3,5-dione derivatives have been obtained by the Diels–Alder reaction and tetrahydro-1H-furo[3,4-c]pyran derivatives could be accessed by the hetero-Diels–Alder cycloaddition.

4-aroyl-5-aryl-2,3-furandiones and N,N-dialkyl urea combine with loss of water yielding the pyrrole2,3-dione derivatives in moderate yields (47-68%). Then, these compounds were converted into 2(1H)quinoxalinones with various 1,2-phenylenediamines. The structures and characterizations of the synthesized compounds were established by the Hand C-NMR, IR and elemental analysis.

ABSTRACT A series of 6'-chloro-1',1'-dioxospiro[4H-benzo[d][1,3,7]oxadiazocine-4,3'(2'H)-[1,4,2]benzodithiazine]-2,6(1H,5H)dione derivatives have been synthesized from isatoic anhydride and 3-(R2-amino)-1,4,2-benzodithiazine 1,1-dioxides. Some synthetic limitations are discussed on the basis of quantum chemical calculations performed by use of the Hartree-Fock method. GRAPHICAL ABSTRACT

A novel acceptor, (3E,7E)-3,7-bis(2-oxoindolin-3-ylidene)-5,7-dihydropyrrolo[2,3-f]indole-2,6(1H,3H)-dione, was reported. Donor-acceptor (D-A) polymer semiconductors using this new building block showed high ambipolar charge transport performance with hole and electron mobilities up to 0.19 and 0.09 cm(2) V(-1) s(-1), respectively, in thin film transistors.