The role of substituents and solvents in promoting "medium-size" ring-chain tautomerism
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00299a036
Cited by 6 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
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3. The Mitsunobu reaction of ortho-ethers of secondary benzylic alcohols. Concise enantioselective synthesis of a key intermediate of the novel β-adrenergic receptor antagonist MY336-a;Tetrahedron Letters;1996-07
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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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