Dienes reaction with vinylcarbene complexes

Fig. 2.37, Formation of cycloheptadienes by reaction of vinylcarbene complexes with 1,3-dienes.

In particular the synthetic approach to dihydrofurans (first equation in Figure 4.23) represents a useful alternative to other syntheses of these valuable intermediates, and has been used for the preparation of substituted pyrroles [1417], aflatoxin derivatives [1418], and other natural products [1419]. The reaction of vinylcarbene complexes with dienes can lead to the formation of cycloheptadienes by a formal [3 + 4] cycloaddition [1367] (Entries 9-12, Table 4.25). High asymmetric induction (up to 98% ee [1420]) can be attained using enantiomerically pure rhodium(II) carboxylates as catalysts. This observation suggests the reaction to proceed via divinylcyclopropanes, which undergo (concerted) Cope rearrangement to yield cycloheptadienes. 

Because of the strong electron-withdrawing effect of the MICO), fragment, reactions of nucleophiles, dienes or 1,3-dipoles with vinylcarbene or alkynylcarbene complexes are usually faster than with the corresponding a,P-unsaturated esters [242,253,264]. 

Heteroatom-substituted vinylcarbene complexes react particularly well with donor-substituted 1,3-butadienes to yield the corresponding cycloheptadienes [264]. Some of these reactions proceed at room temperature. The intermediate divinylcyclopropanes have occasionally been isolated [264]. As indicated in Figure 2.37, for donor-substituted dienes in particular the formation of zwitterionic intermediates... 

The relative ease of ring formation from dienes decreases in the order six->seven->five-membered rings. Hoshi et al. [138] have recently reported the synthesis of a number of disilacycloalkenes via RCM of bis(allyldimethyl-silyl)substituted compounds, with the ruthenium vinylcarbene complex Cl2(PCy3)2Ru(=CHCH=CPh2) used as a catalyst. Successful formation of seven-and eight-membered rings has been achieved under mild reaction conditions. 

Titanium acetylides react with 3-benzyl-tetrahydro-l,3-oxazines and 1,3-oxazolidines to give the corresponding / -aminoacetylenes in modest to good yield.296 Vinyl Ti(iv) species prepared by the alkylation of vinylcarbene complexes with BTCl react with aldehydes to give allylic alcohols. Reaction with terminal alkynes produces conjugated dienes, in which a vinyl group regioselectively bonds to the unsubstituted side of carbon-carbon triple bond.297... 

Barluenga and co-workers extended the scope of [3+4] annulations of chromium vinylcarbenes by using 2-amino-1,3-butadienes as the diene component. In most cases the reaction with this diene is highly diastereoselective and favors the formation of cw-divinylcyclo-propanes that rapidly rearrange to the cycloheptadienes. Furthermore, the amino functionality can be a chiral auxiliary such that an asymmetric [3+4] annulation is achieved. Examples of this approach are shown in Scheme 17. Reaction of the chromium vinylcarbene complex... 

The vinylcarbene complexes Cr(CX))5 =C(OEt)C=CXR) (X = NMe2, OEt R = alkyl, aryl) react with alkynes R OCH to form various cyclopenta[b]pyrans.30S In a two step process, addition of the alkynes NEt20Chfe u> the l-metalla-l,3-diene W(CX))s =C(OEt)CHsCHHi) results in metallatriene species that cyclise U) fwm cyclopentadiene complexes 40. Chromium Fischer type alkoxyalkenyl carbene complexes react with ketoalkynes to fcxm bicyclic lactones in a number of different processes involving 8 and 10-e cyclizations. Various dienyl carbene complexes whose parent in Crortho-substituted aromatic alcohols through a variation upon the more usual benzannulation reaction involving alkyne cycloaddition with carbene complexes. ... 

The diastereoselectivity of Diels-Alder reactions with acyclic sugar-vinylcarbene complexes depends on the nature of the diene. Whereas the tungsten vinylcar-bene 222 gives all four possible diastereomers of cydoadduct 296 upon reaction with cyclopentadiene, only one pair of diastereomers of 297 is observed with 2,3-dimethylbutadiene (Scheme 11.61) [110]. 

Reaction of the carbene complex 148 with alkyne affords vinylcarbene 150 via metallacyclobutene 149. In the intramolecular reaction of enyne 152, catalysed by carbene complex 151, the triple bond is converted to vinylcarbene 153 which then reacts with the double bond to give the conjugated diene 154. Generation of 154 is expected by the formation and cleavage of cyclobutene 155 as a hypothetical intermediate. Based on this reaction, Ru-catalysed intramolecular metathesis of enyne 156 gave the N-containing cyclic diene 157, from which (—)-stemoamide (158) was synthesiszed. The reaction can be understood by assuming the formation of the hypothetical cyclobutene 159 from 156 [52],... 

Addition of diazo compounds to metallic complexes allows the formation of metal carbenoid species which can react with unsaturated molecules to form new carbon-carbon bonds. The Cp RuCl(cod)-catalyzed addition of diazo compoimds to alkynes led to the selective synthesis of functional 1,3-dienes by the combination of two molecules of diazoaUcane and one molecule of alkyne [115,116] [Eqs. (53) and (54)]. The ruthenium carbene, generated from diazo compound, reacts with the C=C bond to produce vinylcarbene intermediate able to add a second molecule of diazo compotmd to generate dienes. The stereoselective formation of these conjugated dienes results from the selective creation of two C=C bonds, probably due to the possibility for (C5Me5)RuCl moiety to accomodate two cis carbene ligands. This reaction occurred with terminal or internal alkynes as well as 1,3-diynes [115] and was applied successfully to alkynylboronates [116]. 

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