DBU-Catalyzed [3+3] and [3+2] Annulation Reactions of Azomethine Ylides with α-Diazocarbonyls asN-Terminal Electrophiles: Modular, Atom-Economical Access to 1,2,4-Triazine and 1,2,4-Triazole Derivatives-Reference-Cited by-同舟云学术

DBU-Catalyzed [3+3] and [3+2] Annulation Reactions of Azomethine Ylides with α-Diazocarbonyls asN-Terminal Electrophiles: Modular, Atom-Economical Access to 1,2,4-Triazine and 1,2,4-Triazole Derivatives

Published:2018-04-18 Issue:11 Volume:360 Page:2172-2177
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Zhang Lu¹,Chen Jia-Jia¹,Liu Sha-Sha²,Liang Yong-Xin¹,Zhao Yu-Long¹

Affiliation:

1. Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis; Faculty of Chemistry; Northeast Normal University; Changchun 130024 People's Republic of China

2. School of Geographical Sciences; Northeast Normal University; Changchun 130024 People's Republic of China

Funder

National Natural Sciences Foundation of China

Natural Sciences Foundation of Jilin Province

Publisher

Wiley

Subject

General Chemistry

Reference79 articles.

1. A mononuclear Cu(II) complex with 5,6-diphenyl-3-(2-pyridyl)-1,2,4-triazine: Synthesis, crystal structure, DNA- and BSA-binding, molecular modeling, and anticancer activity against MCF-7, A-549, and HT-29 cell lines

2. Anticonvulsant evaluation of clubbed indole-1,2,4-triazine derivatives: A synthetic approach

3. Design, synthesis and biological evaluation of novel anti-cytokine 1,2,4-triazine derivatives

4. In vitro antitumor activity evaluation of some 1,2,4-triazine derivatives bearing piperazine amide moiety against breast cancer cells

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