Terminal environmentally friendly

A rapid MW-assisted palladium-catalyzed coupling of heteroaryl and aryl boronic acids with iodo- and bromo-substituted benzoic acids, anchored on TentaGel has been achieved [174]. An environmentally friendly Suzuki cross-coupling reaction has been developed that uses polyethylene glycol (PEG) as the reaction medium and palladium chloride as a catalyst [175]. A solventless Suzuki coupling has also been reported on palladium-doped alumina in the presence of potassium fluoride as a base [176], This approach has been extended to Sonogashira coupling reaction wherein terminal alkynes couple readily with aryl or alkenyl iodides on palladium-doped alumina in the presence of triphenylphosphine and cuprous iodide (Scheme 6.52) [177]. 

The reaction of nitrones with terminal alkynes proceeds in excellent yields and high purity, in the presence of stoichiometric quantities of diethylzinc and zinc triflate (219, 661-663). To optimize the process of diastereoselective addition of terminal alkynes to chiral nitrones, ZnCl2 and NEt3 in toluene were used. This reaction protocol is facile to perform, cost-effective and environmental friendly (664). 

Obviously there is a definite need in the fine chemical and pharmaceutical industry for catalytic systems that are green and scalable and have broad utihty [10]. More recently, oxidations with the inexpensive household bleach (NaOCl) catalyzed by stable nitroxyl radicals, such as TEMPO [17] and PIPO [18], have emerged as more environmentally friendly methods. It is worth noting at this juncture that greenness is a relative description and there are many shades of green. Although the use of NaOCl as the terminal oxidant affords NaCl as the by-product and may lead to the formation of chlorinated impurities, it constitutes a dramatic improvement compared to the use of chromium(VI) and other... 

Conversion of 1,3-diketones 315 into 2-substituted 7,8-dihydroquinazolin-5(6//)-ones 569 by a reaction with substituted amidine hydrochloride and dimethylform-amide dimethyl acetal (DMF-DMA) was achieved under MWI and in aqueous media. The aqueous conditions led to an environmentally friendly work-up. Compounds 569 were obtained in 21-68% yields within 2 min (Scheme 112). The reaction is a tandem addition-elimination/cyclodehydration that took place via a Michael addition of the terminal amino group of the substituted amidine to form intermediate 568, followed by an intramolecular cyclodehydration to give dihydroquinazoli-none derivatives 569 (02S1669). 

Synthesis of Triazoles A number of MCRs that use an epoxide-azide-alkyne Cu(I)-catalyzed cycloaddition sequence to provide substituted p-hydroxy-l,2,3-triazoles 70 (Scheme 3.36) have been recently developed. The azida-tion of an epoxide with sodium azide to give 2-azidoalcohols and subsequent reaction with a terminal alkyne have been carried out under mild conditions in environmentally friendly solvents, such as water, using the catalytic system CuSO sodium ascorbate [65] (see the example depicted in Scheme 3.36) [65a] or a porphyrinatocopper(II) complex... 

Environmentally Friendly Terminal Oxidants 7 TaUel.1 Asymmetric dihydroxylation of different alkenes using NaOCI as the terminal oxidant.. ... 

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