The title compound, C(19)H(12)F(3)NO(4), was synthesized by the reaction of 5-(4-fluoro-phen-yl)-2-furan-methanol and 2,6-difluoro-benzoyl-isocyanate. The seven atoms of the fluorophenyl group are disordered over two positions with site occupancy factors ca 0.6 and 0.4. The dihedral angle between the furan and fluorophenyl rings is 1.58°. In the crystal structure, the mol-ecules are linked via ...

A novel tandem imination-isocyanate-mediated annulation was explored. Ionic liquid-immobilized 2-aminobenzimidazoles react sequentially with aldehydes and isocyanates to give highly functionalized benzimidazole-embedded triazines. The second-stage transformation revealed that the formation of triazinone functionality is entirely regioselective to allow rapid assembly of biologically interesting...

A new cyclic nitrone spin trap, [4-(3',3'-dibutyl-2'-oxy-3'H-isoindol-5'-yloxy)butyl]triphenylphosphonium bromide (MitoSpin), bearing a lipophilic cation has been prepared by a route that involves a novel Parham-type lithiation-cyclization of an isocyanate to give the isoindolinone core. MitoSpin accumulates in a membrane potential dependent way in energized mitochondria and its oxidation could...

Hydroboration of the electron poor phosphine (1-propenyl)P(C(6)F(5))(2) with Piers' borane [HB(C(6)F(5))(2)] gave the geminal frustrated Lewis pair (C(6)F(5))(2)P-CH(Et)-B(C(6)F(5))(2). It undergoes 1,2-addition reactions to an alkene and an alkyne and to the C=N bond of an isocyanate. With mesityl azide it undergoes a 1,3-addition reaction.

The synthesis and isolation of the 2-arsaethynolate anion, AsCO(-) , and its subsequent reactivity towards heteroallenes is reported. Reactions with ketenes and carbodiimides afford four-membered anionic heterocycles in formal [2+2] cycloaddition reactions. By contrast, reaction with an isocyanate yielded a 1,4,2-diazaarsolidine-3,5-dionide anion and the unprecedented cluster anions As10 (2-) a...

A unified strategy for the synthesis of congeners of the prenylated indole alkaloids is presented. This strategy has yielded the first synthesis of the natural product (-)-17-hydroxy-citrinalin B as well as syntheses of (+)-stephacidin A and (+)-notoamide I. An enolate addition to an in situ generated isocyanate was utilized in forging a key bicyclo[2.2.2]diazaoctane moiety, and in this way con...

1.1 Chemical and physical data 1.1.1 Nomenclature Chem. Abstr. Serv. Reg. No.: (a) 101-68-8 (monomer) and (b) 26447-40-5 Chem. Abstr. Name: 1,1′-Methylenebis(4-isocyanatobenzene) IUPAC Systematic Names: For 101-68-8: isocyanic acid, methylenedi-paraphenylene ester Synonyms: Bis(1,4-isocyanatophenyl)methane; diphenylmethane diisocyanate; MDI; methylenedi-para-phenylene isocyanate and for 26447-4...