Studies on the Regioselective Nucleophilic Aromatic Substitution (SNAr) Reaction of 2-Substituted 3,5-Dichloropyrazines-Reference-Cited by-同舟云学术

Studies on the Regioselective Nucleophilic Aromatic Substitution (SNAr) Reaction of 2-Substituted 3,5-Dichloropyrazines

Published:2013-04-19 Issue:9 Volume:15 Page:2156-2159
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Scales Stephanie¹,Johnson Sarah¹,Hu Qiyue¹,Do Quyen-Quyen¹,Richardson Paul¹,Wang Fen¹,Braganza John¹,Ren Shijian¹,Wan Yadong¹,Zheng Baojiang¹,Faizi Darius¹,McAlpine Indrawan¹

Affiliation:

1. La Jolla Laboratories, Pfizer, Inc., 10770 Science Center Drive, San Diego, California 92121, United States, and WuXi App Tec Co., Shanghai, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol4006695

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2. The formal total synthesis of dragmacidin B, trans-dragmacidin C, and cis- and trans-dihydrohamacanthins A

3. An Efficient Protocol for the Synthesis of Unsymmetrical Pyrazines. Total Synthesis of Dihydrocephalostatin 11

4. Design, Synthesis, and Structure−Activity Relationships of Novel 2-Substituted Pyrazinoylguanidine Epithelial Sodium Channel Blockers: Drugs for Cystic Fibrosis and Chronic Bronchitis

5. Prediction of the Aroma Quality and the Threshold Values of Some Pyrazines Using Artificial Neural Networks

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