Cope chloride

The resulting solution is approximately equivalent to 50 ml. of the commercial palladium chloride solution (p. 32) suggested by Hartung and Cope. ... 

As a continuation to the studies by Darwish and Braverman on the [2,3]-sigmatropic rearrangement of allylic sulfinates to sulfones, and in view of its remarkable facility and stereospecificity (see Chapter 13), Braverman and Stabinsky investigated the predictable analogous rearrangement of allylic sulfenates to sulfoxides, namely the reverse rearrangement of that attempted by Cope and coworkers . These authors initiated their studies by the preparation of the claimed allyl trichloromethanesulfenate using the method of Sosnovsky . This method involves the reaction between trichloro-methanesulfenyl chloride and allyl alcohol in ether at 0 °C, in the presence of pyridine (equation 6). 

An interesting application of a 1,2-disubstituted cyclopropanol in a seven-membered ring-annelation methodology has been developed by Cha et al. [82], The cyclopropanol 124, obtained from methyl 1-cyclopentenecarboxylate (123) and 4-(triisopropylsilyloxy)-butylmagnesium chloride, was converted to a 1,2-dialkenylcyclopropanol bis-silyl ether, which, by a subsequent facile Cope rearrangement, afforded the cycloheptadiene-anne-lated cyclopentane derivative 125 in 32% overall yield (Scheme 11.32). 

In addition to a-allenic a-amino acids, the corresponding allenic derivatives of y-aminobutyric acid (GABA) have also been synthesized as potential inhibitors of the pyridoxal phosphate-dependent enzyme GABA-aminotransferase (Scheme 18.49) [131,138-142]. The synthesis of y-allenyl-GABA (152) and its methylated derivatives was accomplished through Crabbe reaction [131], aza-Cope rearrangement [138] and lactam allenylation [139], whereas the fluoroallene 153 was prepared by SN2 -reduc-tion of a propargylic chloride [141]. 

The kinetic preference for cis- over imns-olefin elimination from acyclic compounds is rare. Cope and co-workers 91) reported a slight preference for cis- over irans-2-butene and 2-pentene in the thermal decomposition of the quaternary ammonium hydroxides, and Andr u and co-workers 92,93) found a preponderance of cis- over trons-2-butene in the elimination of hydrogen chloride from 2-chlorobutane over solid catalysts. Neureiter and Bordwell 94) found the formation of cis-2-butene rather than alkene from a-chlorosulfone on treatment with alkali ... 

Lantos and colleagues reported a different imidazole synthesis via hetero-Cope rearrangement. Oximes 116 reacted with benzenecarboxidoyl chloride affording adducts 117 that readily underwent a [3,3]-sigmatropic rearrangement at high temperatures (equation 35) to substituted imidazoles 118. 

The reaction of Af,Af-dimethyl-( )-styrylamine (73) with a halogen-substituted methanesulfonyl chloride allowed the first stereoselective formation of the halogenated thietane 1,1-dioxide 74, which then could be converted to the corresponding thiete sulfone 75 via a Cope elimination of the corresponding AT-oxide. ... 

A three-step synthesis starts from cyclododecanone. Reaction with chlorine gives 2-chlorocyclododecanone which is reacted with 2 mol of vinyl magnesium chloride to give 1,2-divinylcyclododecan-l-ol. This is finally converted into 5-cyclohexadecen-l-one by an oxy-Cope rearrangement [126] ... 

The above procedure is essentially that described by Cope et al.2 Ethyl (1-phenylethylidene) cyanoacetate has been prepared also by condensing acetophenone with ethyl cyanoacetate in the presence of zinc chloride and aniline.3... 

A large number of alkyl-substituted styrene and p-methoxy-styrene oxidra have been ieomerizod in various laboratories, notably those of Tiffeneau, ElieL and Cope. Among the catalysts found to be effective in this connexion are magnesium bromide, aluminum chloride, and boron trifluoride. Only a few illustrative examples are cited in tbe text, although a larger compilation may be found in Table 10. 

E)-(Carboxyvinyl)trimethylam-monium betaine, 67 Ethyl 3,3-diethoxyacrylate, 131 Potassium hydride, 257 aza-Claisen rearrangement L-Valinol, 341 Cope rearrangement Ferric chloride, 133 oxy-Cope rearrangement Potassium hydride, 257 Silver(I) trifluoromethanesulfonate, 274... 

The allyl chloride 353 is prepared from diprenyl ether (352), and its Pd-catalysed 1,4-elimination in the presence of AcONa affords the conjugated diene 354. Citral (355) is obtained by the consecutive Claisen and Cope rerrangements of 354 [168],... 

Palladation of an arene is a very facile reaction when, before the C-H activation step, coordination of palladium to a nearby ligand functionality in the molecule occurs. The first report of a stoichiometric intramolecular palladation is probably the reaction of diazobenzene and palladium chloride by Cope in 1967 [6a], Intramolecular palladation is a widespread reaction that has often been used as a starting point for synthesizing new molecules using insertion reactions in the arylpal-... 

The preparation of organopalladium compounds by exchange reactions of palladium salts and organo-lead, -tin, or -mercury compounds is apparently not the only way that they can be obtained but it does seem to be the most useful way. Convincing evidence is now available to show that direct metalation of aromatic compounds with palladium salts (palladation) can occur. Since the initial report of Cope and Siekman 32> that palladium chloride reacted readily with azobenzene to form an isolable chelated, sigma-bonded arylpalladium compound, several additional chelated arylpalladium compounds have been prepared. 

A new synthesis of reserpine (Scheme 19)60 makes use of a very neat synthesis of cw-hydroisoquinoline derivatives, e.g. (Ill), by means of a Diels- Alder /Cope rearrangement sequence. Manipulation of (111) by unexceptional methods then gives (112), which possesses the required stereochemistry in ring E. Oxidative cyclization of (112) affords 3-isoreserpinediol (113) but, unfortunately, some inside isomer, originating from the cyclization of C-2 with C-21, is also obtained. The synthesis also loses some elegance in the multi-stage conversion of 3-isoreserpinediol into 3-isoreserpine (114), since, in the Swem oxidation of the C-16 aldehyde cyanhydrin by means of DMSO with oxalyl chloride as activator, the over-oxidized products (115) and (116) were obtained. However, reduction of (115) gave 3-isoreserpine (114), which has previously been converted into reserpine by four different methods. 

Substituted a-benzylacetoacetic esters have usually been prepared by the general method of Leuchs,4 in which ethyl aceto-acetate is alkylated in ethanol solution with benzyl chloride and sodium ethoxide. The present method is based upon Cope s 6 procedure for the condensation of carbonyl compounds with ethyl acetoacetate, followed by catalytic reduction of the condensation product. 

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