Synthesis and ring—Chain tautomerism of angularly substituted cycloalkane-fused tetrahydro-1,3-oxazines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Synthesis, Stereochemistry and Transformations of Cyclopentane-, Cyclohexane-, Cycloheptane-, and Cyclooctane-Fused 1,3-Oxazines, 1,3-Thiazines, and Pyrimidines
2. Oxidation of isoxazolidines with peroxy acids. Nitrones and N-hydroxy-1,3-tetrahydrooxazines
3. Stereospecific syn-acylamidation of olefins
4. 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.
5. Ring-chain tautomerism in 1,3-oxazines
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