The acid-induced decomposition of 7-substituted 3-diazo-2-norbornanones. Kinetic studies
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. P. Yates and J.D. Kronis, Tetrahedron Lett., submitted.
2. The Acid-Catalyzed Decomposition of 3-Diazonorcamphor. A Novel Rearrangement
3. Substituent effects on the acid-catalyzed decomposition of 3-diazo-2-norbornanones
4. L'hydrolyse acide des diazoc�tones alcoyl�es: Formation d'ions ?-acylcarbonium secondaires
5. Hydrolyse acide des diazocétones secondaires: Participation des nucléophiles
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1. LiBF4: a mild and novel reagent for the OH insertion reactions of α-diazoketones;Tetrahedron Letters;2003-07
2. Indium triflate: a mild and efficient Lewis acid catalyst for O–H insertion reactions of α-diazo ketones;Tetrahedron Letters;2002-04
3. Synthetic applications of the O-H insertion reactions of carbenes and carbenoids derived from diazocarbonyl and related diazo compounds;Tetrahedron;1995-10
4. Addendum;Diazo Compounds;1986
5. Aliphatic diazo compounds. XIV. The synthesis of 7-substituted 3-diazo-2-norbornanones and the infrared and proton and carbon-13 nuclear magnetic resonance spectra of these diazo ketones and their precursors;Canadian Journal of Chemistry;1984-09-01
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