Diene titanium compounds

Modified T) -titanium compounds have been prepared from exocyclic dienes. The compound (123, n = 3) is an example it is prepared (equation 47) by addition of Bu MgCl to a solution of 1-vinylcyclopen-tene (122, n = 3) and (T) -C5H5)2TiCl, Its reaction with propanal takes place regiospecifically at the carbon atom belonging to the cycle, in 86% yield, affording the sole erythro compound (124, n = 3) (equation... 

In the broadest sense, Ziegler Natta catalysts may be regarded as combinations of Group IV-VIII transition metal compounds with Group I-III organometallics which can effect polymerization of olefins and dienes under relatively mild conditions of temperature and pressure [82,83]. Titanium compounds and aluminum alkyls are used most frequently in commercial polyolefin processes. Both titanium and vanadium compounds are used in conjunction with aluminum alkyls in catalyst systems for synthetic rubber/elastomers. 

There are a few examples of monocyclopentadienyl compounds that catalyze non-conjugated dienes. The cationic titanium compound [Cp TiMe2] [172] and mono(pentamethylcyclopentadienyl)yttrium alkoxides [53] catalyzed cyclopolymerization of 1,5-hexadiene, whereas neither of them gave highly stere-oregulated polymers. 

Danishefsky s diene 154 DBFOX 232 dendrimers 229 DPT calculations 308 diacetone glucose derived-titanium(IV) 178 diastereoselectivity 216 diazo compounds 242 diazoalkane cycloadditions 278 diazoalkanes 213, 231 (R,R)-4,6-dibenzofurandiyl-2,2 -bis(4-phenylox-azoline) 250... 

Alternating Copolymerization. In the last part of this paper we would like to refer briefly to our findings in connection with the alternating copolymerization of dienes with olefins. The alternating copolymerization of butadiene with propylene was first investigated in 1969 by Furukawa and others (15, 16, 17). They used catalyst systems based on titanium or vanadium compounds. 

Titanium silicate molecular sieves not only catalyze the oxidation of C=C double bonds but can be successfully employed for the oxidative cleavage of carbon-nitrogen double bonds as well. Tosylhydrazones and imines are oxidized to their corresponding carbonyl compounds (243) (Scheme 19). Similarly, oximes can be cleaved to their corresponding carbonyl compounds (165). The conversion of cyclic dienes into hydroxyl ketones or lactones is a novel reaction reported by Kumar et al. (165) (Scheme 20). Thus, when cyclopentadienes, 1,3-cyclohexadiene, or furan is treated with aqueous H202 in acetone at reflux temperatures for 6 h in the presence of TS-1, the corresponding hydroxyl ketone or lactone is obtained in moderate to good yields (208). 

In Section 9.2, intermolecular reactions of titanium—acetylene complexes with acetylenes, allenes, alkenes, and allylic compounds were discussed. This section describes the intramolecular coupling of bis-unsaturated compounds, including dienes, enynes, and diynes, as formulated in Eq. 9.49. As the titanium alkoxide is very inexpensive, the reactions in Eq. 9.49 represent one of the most economical methods for accomplishing the formation of metallacycles of this type [1,2]. Moreover, the titanium alkoxide based method enables several new synthetic transformations that are not viable by conventional metallocene-mediated methods. 

The mode of reaction of titanacydobutenes with carbonyl compounds is largely dependent on steric factors (Scheme 14.31) [72]. Ketones and aldehydes tend to insert into the titanium—alkyl bond of 2,3-diphenyltitanacydobutene, and homoallylic alcohols 70 are obtained by hydrolysis of the adducts 71 [65a,73]. On the contrary, when dialkyl-substi-tuted titanacydobutenes are employed, the reaction with aldehydes preferentially proceeds through insertion into the titanium—vinyl bond. Thermal decomposition of the adducts 72 affords conjugated dienes 73 with E-stereoselectivity as a result of a concerted retro [4+2] cycloaddition [72]. 

The initial work on the asymmetric [4-1-2] cycloaddition reactions of A -sulfinyl compounds and dienes was performed with chiral titanium catalysts, but low ee s were observed <2002TA2407, 2001TA2937, 2000TL3743>. A great improvement in the enantioselectivity for the reaction of AT-sulfinyl dienophiles 249 or 250 and acyclic diene 251 or 1,3-cyclohexadiene 252 was observed in the processes involving catalysis with Cu(ll) and Zn(ii) complexes of Evans bis(oxazolidinone) (BOX) ligands 253 and 254 <2004JOC7198> (Scheme 34). While the preparation of enantio-merically enriched hetero-Diels-Alder adduct 255 requires a stoichometric amount of chiral Lewis acid complex, a catalytic asymmetric synthesis of 44 is achieved upon the addition of TMSOTf. 

The homoleptic (see Homoleptic Compound) titanium diene complex (j " -r-BuCH=CHCH=CHBu-t)2Ti (11) has been prepared by the condensation ofelectron-beam vaporized titanium with an excess of 1,4-di-t-butylbuta-1,3-diene" (see Metal Vapor Synthesis of Transition Metal Compounds). The bis-diene dmpe complex Ti(dmpe)( " -C4H6)2Ti (12) has been prepared by the reduction of TiCl4(dmpe) with Na/Hg in the presence of butadiene, and by the reduction of TiCLi with CH2=CHLi in the presence of dmpe. ... 

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