Corrigendum to “Microwave assisted organic synthesis—a review”[Tetrahedron 57 (2001) 9225–9283]

Concise, Asymmetric, Stereocontrolled Total Synthesis of Stephacidins A, B and Notoamide B

“…To this end, we have taken advantage of microwave heating in order to facilitate the desired aromatic Claisen and N-Boc deprotection. 23 With the use of a microwave reactor, the propargyl ether 17 in MeCN was heated at 180 °C for 20 min to afford the desired product 18 in 95% yield. Use of microwave heating for this reaction not only greatly reduced the reaction time but also increased the yield.…”

Application of “Click” Chemistry in Solid Phase Synthesis of Alkyl Halides

“…It can be concluded that all the previous conventionally heated reaction can be easily performed by microwave heating. 24 Many microwave assisted solid phase reactions have been reported in recent years which may include cellular uptake, and cytotoxicity studies of cymantrene-peptide bioconjugates, 25 solid-phase synthesis of 5-arylhistidines via a microwave-assisted Suzuki-Miyaura cross-coupling, 26 synthesis of 1,2,4-oxadiazoles using polymer-bound triphenylphosphine reagent. 27 Recently solid-phase organic syntheses (SPOS) is evolving as a means to facilitate the manipulation of compound libraries via combinatorial chemistry.…”

Synthesis, Characterization and Antimicrobial Activities of 1,2,4-Triazole /Isatin Schiff bases and their Mn(II), Co(II) complexes

“…In recent years Microwave assisted reactions have attracted researchers much interest because of simplicity of operation, enhanced reaction rates, high yields, improved selectivity [20][21] and environmental friendly reaction condition [22][23][24] . The reactions, which are not possible under normal conditions,can be overcome by high-energy microwave irradiation.Thereforwe have made efforts to develop and optimize anew environmentally benign method using microwave irradiation in our laboratory and finally 3-substituted-4-amino-5-mercapto-1,2,4-triazole 25 and isatin derivatives have been synthesized.…”