Ring opening of 3-methoxyacenaphthylene-1,2-dione. Application of 13C-2D-inadequate-N.M.R. spectroscopy to structure assignment of some substituted naphthalenes.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Ueber sauerstoffhaltige Derivate des Acenaphtens
2. An Improved Synthesis of 1,8-Naphthaldehydic Acid
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4. Carbon-13 NMR studies of substituted naphthalenes. I—complete assignments of the13C chemical shifts with the aid of deuterated derivatives
Cited by 4 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. Structure determination using the NMR “INADEQUATE” technique;Advances in Molecular Structure Research Volume 2;1996
2. Structure determination of substituted naphthalenes by nuclear overhauser enhancement measurements;Tetrahedron;1992-03
3. Studies on a Simple Route to a Bicyclic Reserpine Intermediate;Synthetic Communications;1989-11
4. ChemInform Abstract: Ring Opening of 3-Methoxyacenaphthylene-1,2-dione. Application of13C- 2D-Inadequate-NMR Spectroscopy to Structure Assignment of Some Substituted Naphthalenes.;Chemischer Informationsdienst;1986-12-16
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