23. Reactivity of peri-substituted naphthalenes. Part I. Displacement of the nitro-group in 8-nitro-1-naphthoic acid by thionyl halides to form 8-chloro- and 8-bromo-naphthoic acids-Reference-Cited by-同舟云学术

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23. Reactivity of peri-substituted naphthalenes. Part I. Displacement of the nitro-group in 8-nitro-1-naphthoic acid by thionyl halides to form 8-chloro- and 8-bromo-naphthoic acids

Published:1932 Issue: Volume: Page:175
ISSN:0368-1769
Container-title:Journal of the Chemical Society (Resumed)
language:en
Short-container-title:J. Chem. Soc.

Author:

Rule H. Gordon,Barnett A. John G.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1932/JR/JR9320000175

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Total Synthesis of the Aristolochic Acids, Their Major Metabolites, and Related Compounds;Chemical Research in Toxicology;2014-06-11

2. Methods of peri-annulation of five- and six-membered carbocyclic and nitrogen containing heterocyclic fragments;Review Journal of Chemistry;2012-07

3. Synthesis and pharmacology of 1-alkyl-3-(1-naphthoyl)indoles: Steric and electronic effects of 4- and 8-halogenated naphthoyl substituents;Bioorganic & Medicinal Chemistry;2012-03

4. 8-Chloro- and 5,8-Dichloro-1-naphthoic Acids;Organic Preparations and Procedures International;2010-10-04

5. DNA adducts of aristolochic acid II: total synthesis and site-specific mutagenesis studies in mammalian cells;Nucleic Acids Research;2009-10-23

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