Aspects of tautomerism. Part 15. Investigations on oxo-participation in δ-oxocarboxylic acid chlorides during their formation and alcoholysis
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1986/P2/P29860000355
Cited by 7 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. Facile aerobic photooxidative oxylactonization of oxocarboxylic acids in fluorous solvents;Green Chemistry;2012
2. Synthesis and Characterization of Nonsymmetric Cyclopentene-Based Dithienylethenes;The Journal of Organic Chemistry;2011-12-14
3. Reducing the Cost, Smell, and Toxicity of the Barton Reductive Decarboxylation: Chloroform as the Hydrogen Atom Source;Organic Letters;2011-03-25
4. 1,5-Diketones from 3,4-dihydropyranones: An application in the synthesis of (±)-α-herbertenol;Tetrahedron;1999-07
5. Recent Developments in Ring–Chain Tautomerism I. Intramolecular Reversible Addition Reactions to the C=O Group**This chapter is the first part of a review that updates an earlier work by R. E. Valters and W. Flitsch, Ring-Chain Tairtomerism (A. R. Katritzky, ed.), Plenum Press, New York and London, 1985. The second part of this review, to be published in a subsequent volume of Advances in Heterocyclic Chemistry, includes data (1982‒1993) for intramolecular reversible addition reactions to C=N, C≡N, C=C, and C≡C groups.;Advances in Heterocyclic Chemistry;1995
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