Carbanions solid supports

Grignard reaction and similar transformations allow C-C bond formation without a palladium catalyst. Grignard reagents and organolithium compounds are very versatile carbanion sources used in the synthesis of acyclic, heterocychc and carbo-cychc compounds. The esters, ketones and aldehydes are more stable when the reaction takes place on solid supports than in the hquid-phase, because this immo-bihzed components are not so sensitive towards water or oxygen. In the total synthesis of (S)-zearalenone (155) on solid supports the Grignard reaction is one of the key steps (Scheme 3.16) [120]. 

Non-oligomeric and air- or moisture-sensitive chemistries such as cycloadditions, cyclizations, and carbanion condensations have already been successfully enabled on solid support, and some recent examples are discussed below. It is anticipated that these studies will be further extended in combinatorial formats and libraries subjected to HTS in the near future. 

Furans. Timm and coworkers have devised a strategy to synthesize 2,5-disubstituted furans using sulfone carbanion-mediated solid support as a traceless linker (Scheme 12.16). They demonstrated the usefulness of the highly reactive basic carbanionic species of the... 

Electrochemical (cyclovoltametric) investigations of the ladder-type poly-(para-phenylene) species 71 support the results of the chemical oxidation (doping) experiments both in solution and in the solid state (film). A reversible oxidation takes place and it is well-separated into two waves especially in the solid-state experiment. These are assigned to the formation of radical cationic (79) and dicationic species (80), respectively. The halfwave potential (E1/2) for the first oxidation wave lies between 0.75 V (solution experiment) and 0.95 V (solid state - film) - versus a standard calomel electrode SCE) [106]. Consequently, one has to search for an alternative synthetic process to generate the ladder-type poly(phenylenemethide)s 77 or polymers containing extended segments of the fully unsaturated structure desired. The oxidation of polymeric carbanions appeared suitable, but it proved necessary to work under conditions which completely exclude water and air. 

It has an NiAs-type structure (Fig. 15-5), and the isolated methyl groups are presumably in the lattice as the pyramidal CHJ ion.35 Sofiium amd potasstuirralkyl5 can be used for metallation reactions- for example, in eq. 6-2. They can also be prepared from Na or K dispersed on an inert support material, and such solids act as carbanionic catalysts for the cyclization, isomerization or polymerization of alkenes. The so-called alfin catalysts for copolymerization of butadiene with styrene or isoprene to give rubbers consist of sodium alkyl (usually allyl) and alkoxide (usually isopropoxide) and NaCl, which are made simultaneously in hydrocarbons.33... 

---