Rearrangements and unusual reductions with sodium hydride and methyl iodide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Carbon-13 nuclear magnetic resonance spectra: V—substituent interactions at 4-substituted adamantanones and bicyclo[2.2.2]octanones
2. Solvolytic behavior of 7,7-dimethoxybicyclo[2.2.1]hept-2-yl tosylates
3. Synthesis of adamantane derivatives. VIII. Novel substitution reaction of adamantanone. A simple synthesis of bicyclo[3.3.1]non-2-ene-7-carboxylic acid
4. The Beckmann rearrangement of adamantanone oxime
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. Unexpected Retroaldol-Aldol Reaction during O-Alkylation of Hydroxylated Vince Lactam Derivatives;The Journal of Organic Chemistry;2015-12-24
2. Face selectivity in the reactions of 2,4-disubstituted adamantanes and their modification by inclusion in β-cyclodextrin solutions;Tetrahedron;2004-10
3. A Convenient Method for the Preparation of 4(e)-Hydroxy-and 4(e)-Methoxyadamantan-2-ones;Synthetic Communications;1990-12
4. ChemInform Abstract: REARRANGEMENTS AND UNUSUAL REDUCTIONS WITH SODIUM HYDRIDE AND METHYL IODIDE;Chemischer Informationsdienst;1979-05-29
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