Solid phase synthesis inorganic based

On the other hand, a traceless solid-phase synthesis of 2,3-disubstituted indoles 115 was developed using PdCl2(PPh3)2 as the precatalyst, tetramethylgaunidine (TMG) as the base and under double coupling conditions. Solution-phase conditions, in this case, caused incomplete reactions, and large quantities of multiple acetylene insertion side products were observed, presumably due to the poor solubility of the inorganic bases. 

Inorganic bases have been also employed in this system. When Butcher first used alkali carbonates [50], it was reported that, in DMF and at ambient temperature, the carbamation of primary and secondary aliphatic amines (or also arylamines) with alkyl halides under a C02 atmosphere (0.1 MPa) was effectively promoted by Cs2C03 [50, 51]. The Cs+ cations in the solvent used (DMF) did not form ion pairs with counterions, and favored the formation of naked carbamate anions that were more reactive at the O-ends with alkyl halides. Jung further found that the addition of tetrabutylammonium iodide (TBAI) to the system RR NH/ C02/RX/Cs2C03/DMF promoted the carbamation process with a higher yield and selectivity with respect to N-alkylation [51]. The process has been successfully extended to the synthesis of carbamate functionalities on solid phases. In this case, resin-bound carbamates are readily released from the resin by treatment with LiAlH4 in THF, yielding the respective N-methyl secondary amines [51]. 

Generally, solution-based approaches for the generation of inorganic split and pool libraries have substantial advantages over approaches where solid phases are introduced as chemical sources during the different synthetic steps. Solution chemistry offers, potentially, a wide range of synthetic opportunities that can be exploited not only for the purpose of parallel synthesis but also for synthetic steps for Split Pool library creation. 

Even carbowax (a chemically and thermally stable poly(ethylene glycol), when adsorbed on an inorganic salt with no other solid support, may act as a very efficient gas-solid phase-transfer catalyst. This system has been employed, for example, in the Williamson synthesis of ethers and thioethers, starting from alkyl halides and phenols or thiols in the presence of potassium carbonate as a base Gas-solid PTC shows the advantage that pure products are obtained directly, due to the absence of aqueous and organic solvents. 

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