222721-04-2Relevant articles and documents
Alkylidene and metalacyclic complexes of tungsten that contain a chiral biphenoxide ligand. Synthesis, asymmetric ring-closing metathesis, and mechanistic investigations
Tsang, W. C. Peter,Hultzsch, Kai C.,Alexander, John B.,Bonitatebus Jr., Peter J.,Schrock, Richard R.,Hoveyda, Amir H.
, p. 2652 - 2666 (2003)
Two complexes that contain the racemic or enantiomerically pure (S) form of the 3,3′-di-tertbutyl-5,5′,6,6′-tetramethyl-1, 1′-biphenyl-2,2′-diolate (Biphen2-) ligand, W(NAr)(CHCMe2Ph)(Biphen) (2a) and W(NAr′)(CHCMe2Ph)(Biphen) (2b) (Ar = 2,6-i-Pr2C6H3; Ar′ = 2,6-Me2C6H3), were prepared and shown to be viable catalysts for several representative ring-closing reactions to give products in good yields in most cases and high % ee in asymmetric reactions. Exploration of the reaction between 2a and a stoichiometric amount of one desymmetrization substrate allowed two intermediate tungstacyclobutane complexes to be observed, in addition to the final and quite stable tungstacyclobutane complex formed in a reaction between the ring-closed product and a tungsten methylene complex. Reactions involving 13C labeled ethylene allowed for the observation of an unsubstituted tungstacyclobutane complex, an ethylene complex, an unsubstituted tungstacyclopentane complex, and a heterochiral dimeric form of a methylene complex. The tungstacyclopentane complex was found to catalyze the dimerization of ethylene to 1-butene slowly.
