Substituent and solvent isotope effects on the reaction of 2-alkylnaphth[1,8-de]-1,3-oxazines to 1-hydroxy-8-acylaminonaphthalenes through reversible formation of a cyclic tetrahedral addition intermediate
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1996/P2/P29960001105
Cited by 3 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. ChemInform Abstract: Substituent and Solvent Isotope Effects on the Reaction of 2- Alkylnaphth(1,8-de)-1,3-oxazines to 1-Hydroxy-8-acylaminonaphthalenes Through Reversible Formation of a Cyclic Tetrahedral Addition Intermediate.;ChemInform;2010-08-05
2. Theoretical calculations of minimum energy structures and thermodynamics for the formation of cyclic amidines and imidates by intramolecular nucleophilic addition/elimination reactions;Journal of the Chemical Society, Perkin Transactions 2;1998
3. Kinetics and mechanism of the addition of water and ring-opening of 2-methyl- and 2-aryl-4H-3,1-benzoxazines to 2-aminobenzyl esters in the acidic pH range; change in rate-limiting step with buffer concentration and evidence for a tetrahedral carbonyl addition intermediate;Journal of the Chemical Society, Perkin Transactions 2;1997
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