Synthesis of Multisubstituted 2-Aminopyrroles/pyridines via Chemoselective Michael Addition/Intramolecular Cyclization Reaction-Reference-Cited by-同舟云学术

Synthesis of Multisubstituted 2-Aminopyrroles/pyridines via Chemoselective Michael Addition/Intramolecular Cyclization Reaction

Published:2014-07-25 Issue:16 Volume:16 Page:4186-4189
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Qi Xueyu¹,Xiang Haoyue¹,He Qian¹,Yang Chunhao¹

Affiliation:

1. State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai, 201203, China

Funder

National Natural Science Foundation of China

Ministry of Science and Technology of the People's Republic of China

Shanghai Institute of Materia Medica, Chinese Academy of Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol5018855

Reference40 articles.

1. Structure-based design and synthesis of pyrrole derivatives as MEK inhibitors

2. Synthesis and in vitro antitumoral activity of new hydrazinopyrimidine-5-carbonitrile derivatives

3. Tumor-Targeting with Novel Non-Benzoyl 6-Substituted Straight Chain Pyrrolo[2,3-d]pyrimidine Antifolates via Cellular Uptake by Folate Receptor α and Inhibition of de Novo Purine Nucleotide Biosynthesis

4. Evaluation of the anti-inflammatory activity of some pyrrolo[2,3-d]pyrimidine derivatives

5. Synthesis of 5,7-disubstituted-4-methyl-7H-pyrrolo[2,3-d]pyrimidin-2-amines as microtubule inhibitors

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