Alkaline hydrolysis of dibenzoylaminonaphthalenes in 70%(v/v) Me2SO–H2O and the effect of a neighbouring amide group
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1989/P2/P29890000765
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. Replacement of a Naphthalene Scaffold in Kelch-like ECH-Associated Protein 1 (KEAP1)/Nuclear Factor (Erythroid-derived 2)-like 2 (NRF2) Inhibitors;Journal of Medicinal Chemistry;2018-08-20
2. Probing the structural requirements of non-electrophilic naphthalene-based Nrf2 activators;European Journal of Medicinal Chemistry;2015-10
3. ‘Proton sponge’ amides: unusual chemistry and conversion into superbasic 6,7-bis(dimethylamino)perimidines;Tetrahedron;2013-02
4. Oxidation of 1-amino-4,5-bis(dimethylamino)naphthalene as a route to the double “proton sponges” based on dibenzo[a,h]phenazine and 1,1′-azonaphthalene;Russian Chemical Bulletin;2011-10
5. Kinetics of the alkaline hydrolysis of 1,8-bis(trifluoroacetylamino)naphthalene to 1-amino-8-trifluoroacetylaminonaphthalene in 70%, 80% and 90%(v/v) Me2SO–H2O;J. Chem. Soc., Perkin Trans. 2;1992
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