Microwaves in Organic Synthesis 2012
DOI: 10.1002/9783527651313.ch4
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Nonthermal Effects of Microwaves in Organic Synthesis

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Cited by 19 publications
(6 citation statements)
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“…In Microwaves in Organic Synthesis ; de la Hoz, A., Loupy, A., Eds. ; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, 2013 …”
Section: Thermal Vs Nonthermal Microwave Effectmentioning
confidence: 99%
“…In Microwaves in Organic Synthesis ; de la Hoz, A., Loupy, A., Eds. ; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, 2013 …”
Section: Thermal Vs Nonthermal Microwave Effectmentioning
confidence: 99%
“…Application of MW in organic synthesis is considered as a "green" approach because this frequently permits improving efficiency of the reactions. 19 This technique has been extended to the polycondensation polymers. 21 Syntheses of PBIs by solution polycondensation in PPA using MW have also been reported.…”
Section: Preparation Of Opbi and Cf 3 Pbi Using Mwmentioning
confidence: 99%
“…In recent years, the microwave techniques have been increasingly employed in organic synthesis because it allows increasing the synthesis efficiency and shortening the reaction time. 19 Synthesis of high performance polymers under microwave irradiation (MW) has also been reported. [20][21][22][23] In general, use of MW resulted in an acceleration of the polymerizations and even promoted the formation of polymers with higher molecular weights.…”
Section: Introductionmentioning
confidence: 99%
“…[ 29 ] Microwave transparent solvents can even be advantageous because they allow a specific absorption by the reactants. [ 30 ] Indeed, microwave irradiation of chalcone 11aa in toluene at 250 °C for 1 h resulted in the formation of 12aa and 13aa in a ratio of 0.8:1.0 and a combined yield of 93 % (entry 11), which is even higher than the yield obtained in N,N ‐DEA under otherwise identical conditions (entry 1). Addition of NaOAc did not improve the yield of the flavanone (entry 12).…”
Section: Resultsmentioning
confidence: 97%