Highly N2-Regioselective TsOH-Catalyzed Olefin Hydroamination: Metal-Free Synthesis ofN2-Alkyl-1,2,3-triazoles-Reference-Cited by-同舟云学术

Highly N2-Regioselective TsOH-Catalyzed Olefin Hydroamination: Metal-Free Synthesis ofN2-Alkyl-1,2,3-triazoles

Published:2017-03-21 Issue:6 Volume:6 Page:662-665
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J. Org. Chem.

Author:

Wei Hao¹^ORCID,Hu Qingxia²,Ma Yutao²,Wei Liangming¹,Liu Jiaqiang³,Shi Min²⁴,Wang Feijun²

Affiliation:

1. School of Electronic Information and Electrical Engineering; Shanghai Jiao Tong University; Shanghai 200240 P. R. China

2. Key Laboratory for Advanced Materials; East China University of Science and Technology; 130 Meilong Road Shanghai 200237 P. R. China

3. Department of Oral and Cranio-Maxillofacial, Ninth People's Hospital; Shanghai Jiao Tong University School of Medicine; Shanghai 200011 P. R. China

4. State Key Laboratory of Organometallic Chemistry; Shanghai Institute of Organic Chemistry; Chinese Academy of Sciences; 354 Fenglin Road Shanghai 200032 P. R. China

Funder

National Natural Science Foundation of China

Shanghai Pujiang Program

Medical-Engineering Crossover Fund of Shanghai Jiao Tong University

Publisher

Wiley

Subject

Organic Chemistry

Reference42 articles.

1. Biological Properties of 1H-1,2,3- and 2H-1,2,3-Triazoles

2. Novel Octahydropyrrolo[3,4-c]pyrroles Are Selective Orexin-2 Antagonists: SAR Leading to a Clinical Candidate

3. Substituent variation in azabicyclic triazole- and tetrazole-based muscarinic receptor ligands

4. The First Large-Scale Synthesis of MK-4305: A Dual Orexin Receptor Antagonist for the Treatment of Sleep Disorder

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