The catalytic functionalization of unreactive C− H bonds has recently brought a revolution in
synthetic methodologies for the production of pharmaceuticals and natural products and for …

When RuH2 (CO)(PPh3) 3 was reacted with 2, 2-dimethyl-1-(2-p-tolylphenyl) propan-1-one
(2), the ruthenium− aryloxy complex 3 was obtained in 76% yield. The structure of this …

The performance of certain olefin metathesis reactions catalyzed by Grubbs catalysts has
been enhanced by the simple addition of phenol. Addition of phenol to self-metathesis …

A new method for C–O bond activation of phenolic compounds has been achieved using 2,
4, 6-trichloro-1, 3, 5-triazine to utilize in one-pot Ni-catalyzed deoxygenation and reductive …

Recent developments in ruthenium-catalyzed chemo-, regio-, and stereoselective CC bond
forming reactions as well as a CC bond cleaving reaction via an η3-allylruthenium …

Naphthols efficiently couple with internal alkynes via cleavage of the C–H bond at the peri-
position in the presence of a catalyst system of [IrCl (cod)] 2/PBu t 3 to selectively afford the …

Reactions of S allyl systems (allyl sulphides of R S allyl type, where R= Et, allyl, Ph,
Me3C, Ph3C, as well as of allyl phenyl sulphoxide, allyl phenyl sulphone, 2, 5-dihydro-1, 1 …

The reaction of propargylic alcohols with carboxylic acid, or phenol derivatives, in the
presence of the precatalyst [RuCl (cod)(C5Me5)] leads selectively to a variety of …

Als koordinierende Gruppe unterstützt der Phenolrest in entsprechend substituierten
Cyclobutanonen die RhI‐katalysierte Aktivierung der C‐C‐Bindung zwischen dem Carbonyl …

Allyl carboxylates or ethers react with Ru (cod)(cot)(1)[cod: 1, 5-cyclooctadiene, cot: 1, 3, 5-
cyclooctatriene] in the presence of monodentate tertiary phosphines such as PMe3, PEt3 …