Rate–pH profile for the formation of 1-hydroxy-8-acetylaminonaphthalene from 2-methylnaphth[1,8-de]-1,3-oxazine in aqueous solution; acid catalysis and inhibition and comparison with the reaction of 1-amino-8-trifluoroacetylaminonaphthalene-Reference-Cited by-同舟云学术

Rate–pH profile for the formation of 1-hydroxy-8-acetylaminonaphthalene from 2-methylnaphth[1,8-de]-1,3-oxazine in aqueous solution; acid catalysis and inhibition and comparison with the reaction of 1-amino-8-trifluoroacetylaminonaphthalene

Published:1994 Issue:4 Volume: Page:795-798
ISSN:0300-9580
Container-title:J. Chem. Soc., Perkin Trans. 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Dixon Wendy J.,Hibbert Frank

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1994/P2/P29940000795

Reference12 articles.

1. Cyclic imine formation by intramolecular nucleophilic addition and elimination between an amino group and amide carbonyl; rate–pH profile for the reaction of 1-amino-8-trifluoroacetylaminonaphthalene to 2-trifluoromethylperimidine

2. Mechanism of an intramolecular addition–elimination between amino and amide groups; a biphasic Brønsted plot for acid catalysis as evidence for rate-limiting proton transfer to the addition intermediate

3. Sur L'oxydation du Dihydroxy-1.8-Naphtalène et de Son Éther Monométhylique par L'acide Peracétique

4. BEHAVIOR OF MIXED O-ACYL-N-ACYL DERIVATIVES IN WHICH THE REACTING GROUPS ARE NOT ON ADJACENT CARBON ATOMS1

5. The Metalation of 1-Methoxynaphthalene with n-Butyllithium

Cited by 5 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. Gas-phase thermolysis of 1-acylnaphtho[1,8-de][1,2,3]triazines. Interesting direct routes towards condensed naphtho[1,8-de]heterocyclic ring systems;Tetrahedron;2005-10

2. Formation of a cyclic tetrahedral intermediate by the addition of water to 2-methyl-4H- 3,1-benzoxazine followed by ring opening to 2-aminobenzyl acetate and 2-acetylaminobenzyl alcohol; pH-dependence of rate of reaction and product ratio;Canadian Journal of Chemistry;1999-06-01

3. 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

4. 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

5. 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;Journal of the Chemical Society, Perkin Transactions 2;1996