[2+2] Cycloaddition Reactions with a Tungsten-Stabilized 2<i>H</i>-Phenol

The phenol ligand of the complex TpW(NO)(PMe3)(η2-phenol) exists in solution as its 2H tautomer. This normally inaccessible isomer of phenol undergoes a [2+2] cycloaddition with several ketenes across the C3−C4 bond of the phenol. The resulting cyclobutanone can be selectively reduced with sodium borohydride without disturbing the enone functionality, and the resulting hydroxy[4.2.0]bicyclooctenone, which contains four new stereocenters, may be removed from the metal

[2+2] Cycloaddition Reactions with a Tungsten-Stabilized 2<i>H</i>-Phenol

The phenol ligand of the complex TpW(NO)(PMe3)(η2-phenol) exists in solution as its 2H tautomer. This normally inaccessible isomer of phenol undergoes a [2+2] cycloaddition with several ketenes across the C3−C4 bond of the phenol. The resulting cyclobutanone can be selectively reduced with sodium borohydride without disturbing the enone functionality, and the resulting hydroxy[4.2.0]bicyclooctenone, which contains four new stereocenters, may be removed from the metal

Stereoselective Umpolung Tandem Addition of Heteroatoms to Phenol

Stereoselective Umpolung Tandem Addition of Heteroatoms to Pheno

Stereoselective Umpolung Tandem Addition of Heteroatoms to Phenol

Stereoselective Umpolung Tandem Addition of Heteroatoms to Pheno

Common Electrophilic Addition Reactions at the Phenol Ring: The Chemistry of TpW(NO)(PMe₃)(<i>η</i>²-phenol)

The complex TpW(NO)(PMe3)(η2-benzene) was treated with an excess of phenol to generate TpW(NO)(PMe3)(η2-2H-phenol) as a mixture of two stereoisomers. This complex in the presence of base undergoes reactions with several common classes of electrophiles, including benzaldehyde, alkyl iodides, and Michael acceptors, to form new C−C bonds. Methyl and ethyl iodide react at C2 to form 2-alkyl-2H-phenol complexes, whereas the Michael acceptors react at C4 to give 4-alkyl-4H-phenol complexes. In both cases, the electrophile adds to the complexed phenol stereoselectively, anti to the metal. In the case of benzaldehyde, an aldol condensation reaction occurs at C2 to form a rare example of a thermally stable o-quinone methide complex. Crystal structures of the 2-ethyl-2H-phenol and the phenyl o-quinone methide complexes are included

Single and Double Electrophilic Addition Reactions to the Aniline Ring Promoted by a Tungsten π-Base

Single and Double Electrophilic Addition Reactions to the Aniline Ring Promoted by a Tungsten π-Bas

Single and Double Electrophilic Addition Reactions to the Aniline Ring Promoted by a Tungsten π-Base

Single and Double Electrophilic Addition Reactions to the Aniline Ring Promoted by a Tungsten π-Bas

Stereoselective Umpolung Tandem Addition of Heteroatoms to Phenol

Stereoselective Umpolung Tandem Addition of Heteroatoms to Pheno

Common Electrophilic Addition Reactions at the Phenol Ring: The Chemistry of TpW(NO)(PMe₃)(<i>η</i>²-phenol)

The complex TpW(NO)(PMe3)(η2-benzene) was treated with an excess of phenol to generate TpW(NO)(PMe3)(η2-2H-phenol) as a mixture of two stereoisomers. This complex in the presence of base undergoes reactions with several common classes of electrophiles, including benzaldehyde, alkyl iodides, and Michael acceptors, to form new C−C bonds. Methyl and ethyl iodide react at C2 to form 2-alkyl-2H-phenol complexes, whereas the Michael acceptors react at C4 to give 4-alkyl-4H-phenol complexes. In both cases, the electrophile adds to the complexed phenol stereoselectively, anti to the metal. In the case of benzaldehyde, an aldol condensation reaction occurs at C2 to form a rare example of a thermally stable o-quinone methide complex. Crystal structures of the 2-ethyl-2H-phenol and the phenyl o-quinone methide complexes are included