Vinylidene cycloaddition reactions

The alternating electronic properties of the Co, and Cp atoms in the vinylidene ligand enable dipolar molecules to enter into cycloaddition reactions. Intramolecular [2 + 2]-... 

Two recent publications feature metal vinylidenes functioning as 1,3-dipole equivalents, as in the Cu-catalyzed Huisgen cyclization (Section 9.4.5). Fiirstner and coworkers described intramolecular Diels-Alder reactions of unactivated die-nynes catalyzed via a proposed [4+3]-diene/copper vinylidene cycloaddition [59]. 

The homologous cumulene 44 prepared by an analogous vinylidene insertion reaction is spontaneously transformed to the dimer 45.46 By contrast the stable tert-butyl derivative 46 undergoes thermal cycloaddition at one of the inner double bonds giving 47. The structure of this dimer was confirmed by X-ray diffraction.47... 

The thiolate-bridged diruthenium complex 101 can promote a cycloaddition reaction between propargylic alcohols and 1,3-dicarbonyl compounds to provide 3-acyM//-pyrans in excellent yield (Scheme 33). The reaction proceeds via formation and alkylation of the allenylidene complex 102 to form the vinylidene intermediate 103, which upon cyclization furnishes 4//-pyrans (Scheme 33) <2004JOC3408>. 

F. Cycloaddition Reactions of Ruthenium Acetylide and Vinylidene Complexes... 

Transition metal carbyne complexes are described by the general formula L M=CR where the carbyne ligand (=CR) is bonded to the metal by a metal-carbon triple bond. Transition metal carbene complexes have found numerous applications in synthetic organic chemistry through a variety of carbene transfer and cycloaddition reactions [17]. In contrast, carbyne (L M=CR) and vinylidene (L M=C=CRR ) complexes have far fewer applications, in part because their overall chemistry is significantly less developed [18]. Addition reactions to transition metal vinylidene complexes will be discussed in Chapter 21. The first successful synthesis of a carbyne complex was reported by Fischer and co-workers in 1973 [Eq. (8) 19]. Subsequently, many other carbyne complexes have been synthesized by the classic route of Fischer or by new synthetic methods [20]. 

Also, bi- and trimetallic cumulene complexes, such as M=C=M, M=M=C, M=M=M and M=C=C=M are known. Cationic ruthenium allenylidene complexes are used as catalysts for ring closing metathesis reactions. Nonlinear optical properties have been measured for the Group 6 cumulenylidene complexes. Also, cationic chromium or iron vinylidene complexes undergo [2-1-2] cycloaddition reactions across imines to give fi-lactams. This reaction is useful for the synthesis of j8-lactam antibiotics. ... 

Vinylidene complexes of manganese and rhenium, generated in situ, undergo [2+2] cycloaddition reactions with imines to form 52. ... 

The vinylidene complexes (CO)5W=C=CPh2 react with imines and triphenylketen-imines to give [2+2] cycloadducts AUenylidene complexes of chromium 56 also undergo [2+2] cycloaddition reactions with azomethines at the center C=C bond to give the cycloadducts 57 . 

A [3+2] cycloaddition reaction of the vinylidene cyclopropanes 334 with MeCN does not proceed across either one of the C=C bonds, but occured via ring opening to form the cycloadduct 335 °. ... 

Thiolate-bridged dirutheniutn complexes catalyze the [3-f3] cycloaddition reaction between propargylic alcohols and cyclic 1,3-dicarbonyl compounds to afford 4,6,7,8-tetrahydrochromen-5-ones or 4//-cyclopenta[b]pyran-5-ones [193] and with 2-naphthols or phenols to afford l//-naphtho[2,l-b]pyrans and 4//-l-benzo-pyrans, respectively [194]. This cycloaddition is considered to proceed by stepwise propargylation and intramolecular cyclization (carbon and oxygen nucleophile additions) reactions, where ruthenium allenylidene and vinylidene complexes are the key intermediates (Scheme 57). Enantioselective mthenium-catalyzed [3-f3] cycloaddition of propargylic alcohols with 2-naphthols has also been described [195]. 

Another focus of this chapter is the alkynol cycloisomerization mediated by Group 6 metal complexes. Experimental and theoretical studies showed that both exo- and endo- cycloisomerization are feasible. The cycloisomerization involves not only alkyne-to-vinylidene tautomerization but alo proton transfer steps. Therefore, the theoretical studies demonstrated that the solvent effect played a crucial role in determining the regioselectivity of cycloisomerization products. [2 + 2] cycloaddition of the metal vinylidene C=C bond in a ruthenium complex with the C=C bond of a vinyl group, together with the implication in metathesis reactions, was discussed. In addition, [2 + 2] cycloaddition of titanocene vinylidene with different unsaturated molecules was also briefly discussed. 

Ruthenium vinylidene species can be transformed into small carbocyclic rings via carbocyclization reactions. Ruthenium vinylidene complex 2, generated from the electrophilic reaction of alkyne complex 1 with haloalkanes, was deprotonated with "BU4NOH to give the unprecedented neutral cyclopropenyl complex 3 (Scheme 6.2) [5]. Gimeno and Bassetti prepared ruthenium vinylidene species 4a and 4b bearing a pendent vinyl group when these complexes were heated in chloroform for a brief period, cyclobutylidene products 5a and Sb formed via a [2 + 2] cycloaddition between the vinylidene Ca=Cp bond and olefin (Scheme 6.3) [6]. 

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