Microwave-Assisted and Efficient One-Pot Synthesis of Substituted 1,2,4-Triazoles.

Microwave-Assisted Synthesis of Substitu

Microwave-Assisted Synthesis of Substituted 1,2,4-Triazoles.

✍ Dong-Qing Wu; Jian-Li He; Jun-Ke Wang; Xi-Cun Wang; Ying-Xiao Zong 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Efficient and Regiospecific One-Pot Synt

Efficient and Regiospecific One-Pot Synthesis of Substituted 1,2,4-Triazoles.

✍ Michael J. Stocks; David R. Cheshire; Rachel Reynolds 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

Rapid and Efficient Microwave-Assisted S

Rapid and Efficient Microwave-Assisted Synthesis of 4-Amino-3-mercapto-5-substituted-1,2,4-triazoles.

✍ S. S. Joshi; A. V. Karnik 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 15 KB 👁 2 views

Microwave-Assisted One-Pot Synthesis of

Microwave-Assisted One-Pot Synthesis of 1,2,3,4-Tetrahydrocarbazoles.

✍ Jing Chen; Yongzhou Hu 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 17 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.

Simple and Efficient One-Pot Synthesis o

Simple and Efficient One-Pot Synthesis of 2,4-Diaryl-1,2,3-triazoles.

✍ Wen-Jie Tang; Yong-Zhou Hu 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 19 KB 👁 2 views

Microwave-assisted synthesis of some 1,2

Microwave-assisted synthesis of some 1,2,4-triazol-5-one derivatives

✍ Bahittin Kahveci; Musa Özil; Mevlüt Serdar 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 124 KB 👁 1 views

## Abstract A series of 3‐alkyl(aryl)‐4‐(__p__‐hydroxy‐phenyl)‐4,5‐dihydro‐1__H__‐1,2,4‐triazol‐5‐ones **2** were obtained from the reaction of alkyl (aryl) ester ethoxycarbonyl hydrazones **1** with __p__‐hydroxy aniline. The reaction of **1** with 1,4‐diamino benzene (1:1) to afford 3‐alkyl(aryl)