Download e-book for iPad: Aqueous Microwave Assisted Chemistry: Synthesis and by Rajender S. Varma, Vivek Polshettiwar

By Rajender S. Varma, Vivek Polshettiwar

ISBN-10: 1849730385

ISBN-13: 9781849730389

The calls for for eco-friendly and sustainable artificial equipment within the fields of healthcare and tremendous chemical substances, mixed with the strain to supply those components expeditiously and in an environmentally benign model, pose major demanding situations to the substitute chemical neighborhood. eco-friendly chemistry can steer clear of pollutants through the use of suggestions which are environmentally pleasant via layout and the most effective eco-friendly concepts is using microwave (MW) assisted aqueous artificial protocols. Fusing MW method with water (as a benign response medium) can provide a unprecedented synergistic impression with higher strength than those person parts in isolation. Selective microwave heating might be exploited to enhance a excessive yield protocol and using water expedites the MW-protocol with extra strength potency. This publication presents an summary of some of the approaches built utilizing aqueous microwave chemistry and is written for chemists, chemical engineers and researchers within the early levels who are looking to strengthen sustainable and eco-friendly methods. Written through renowned microwave specialists, the ebook is a finished exam of the sector and is the 1st booklet that bargains strictly with aqueous microwave chemistry and represents an important attempt in the direction of eco-friendly chemistry. It covers all of the microwave-assisted aqueous reactions intensive, together with heterocycle synthesis, steel catalysis, enzyme catalysis, polymer synthesis, nanomaterials synthesis and nano-catalysis. every one bankruptcy includes consultant experimental tactics, assisting the reader speedy mirror a number of the experiments to achieve hands-on event.

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Extra resources for Aqueous Microwave Assisted Chemistry: Synthesis and Catalysis (RSC Green Chemistry Series)

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The combined use of tin and indium metals played a crucial role in the selectivity of the process; transformations mediated exclusively by Sn gave rise to a mixture of the desired homopropargylic alcohols along with their allenyl tautomers. However, sterically demanding benzaldehydes bearing substituents in ortho-position, such as 2,6-dimethoxybenzaldehyde or 2-chlorobenzaldehyde, were also found to favor the formation of allenic side-products, reducing considerably the yields of the corresponding homopropargylic alcohols.

38 case, the use of a mixture of THF–iPrOH–H2O (3 : 1 : 1) as solvent was required to improve the solubility of the reactants. 38, the solid-supported trigalactosylated oligonucleotide 24 could be synthesized in quantitative yield by ‘‘click’’ coupling of the alkyne-bearing oligonucleotide 23 (T12* ¼ dodecathymidine) with the azidefunctionalized galactoside 22. ) as the Cu(I) source. 79 Thus, in a first step, the corresponding organic azides were generated in situ by a Cu(II)-catalyzed diazo transfer reaction from trifluoromethanesulfonyl azide (TfN3) to the amines.

E. 39 High degrees of deuteration (494% D) were reached with both aromatic and aliphatic substrates. As proposed by the authors, the process proceeds through the initial dehydrogenation of the alcohol and subsequent deuteration of the resulting aldehyde. Interestingly, this protocol was successfully applied to optically active alcohols bearing a stereogenic centre at the b-position, but a lower temperature (100 1C, 22 psi) and a longer reaction time (60 min) were necessary in these cases to avoid racemization.

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Aqueous Microwave Assisted Chemistry: Synthesis and Catalysis (RSC Green Chemistry Series) by Rajender S. Varma, Vivek Polshettiwar


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