Straightforward and Highly Efficient Catalyst-Free One-Step Synthesis of 2-(Purin-6-yl)acetoacetic Acid Ethyl Esters, (Purin-6-yl)acetates, and 6-Methylpurines through SNAr-Based Reactions of 6-Halopurines with Ethyl Acetoacetate-Reference-Cited by-同舟云学术

Straightforward and Highly Efficient Catalyst-Free One-Step Synthesis of 2-(Purin-6-yl)acetoacetic Acid Ethyl Esters, (Purin-6-yl)acetates, and 6-Methylpurines through SNAr-Based Reactions of 6-Halopurines with Ethyl Acetoacetate

Published:2009-03-18 Issue:8 Volume:11 Page:1745-1748
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Qu Gui-Rong¹,Mao Zhi-Jie¹,Niu Hong-Ying¹,Wang Dong-Chao¹,Xia Chao¹,Guo Hai-Ming¹

Affiliation:

1. College of Chemistry and Environmental Science, Henan Normal University, Xinxiang 453007, Henan, P. R. China, and School of Chemistry and Chemical Engineering, Henan Institute of Science and Technology, Xinxiang 453003, China.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9002256

Reference60 articles.

1. Analogs of 6-methyl-9.beta.-D-ribofuranosylpurine

2. EFFECTS OF 6-MERCAPTOPURINE AND ANALOGS ON EXPERIMENTAL TUMORS

3. Synthesis of 6-alkenyl- and 6-alkynylpurines with cytokinin activity

4. Antioxidant activity of synthetic cytokinin analogues: 6-alkynyl- and 6-alkenylpurines as novel 15-Lipoxygenase inhibitors

5. 9-Benzylpurines with inhibitory activity against Mycobacterium tuberculosis

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