1,3-Dipolar cycloaddition of nitrile oxides toN-vinylcarbazole: Regioselective formation of 5-(9-carbazolyl)-Δ2-isoxazolines
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570260146/fullpdf
Reference6 articles.
1. 1.3-Dipolar Cycloaddition of Nitrile Oxides to Chlorosulfonyl Isocynate: Selective Formation of 3-Aryl Substituted 1,2,4-Oxadiazolin-5-ones
2. PMR and UV-vis spectroscopic studies on structure of some N-vinylcarbazoles
3. Origin of reactivity, regioselectivity, and periselectivity in 1,3-dipolar cycloadditions
4. Frontier molecular orbitals of 1,3 dipoles and dipolarophiles
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. Synthesis of Assemblies of Isoxazole and Azoles Based on 1,3-Dipolar Cycloaddition Reaction of Enamines with Nitrile Oxides;Chemistry of Heterocyclic Compounds;2016-09
2. Cycloaddition Reactions of Nitrile Oxides with Alkenes;Advances in Heterocyclic Chemistry;1994
3. Perkin communications. Biocatalytic asymmetric cycloaddition of benzonitrile N-oxides to N-vinylcarbazole;Journal of the Chemical Society, Perkin Transactions 1;1990
4. Baker's yeast catalyzed asymmetric cycloaddition of nitrileoxides to CC bond : Improved chiral recognition by using β-cyclodextrin;Tetrahedron Letters;1990-01
5. ChemInform Abstract: 1,3-Dipolar Cycloaddition of Nitrile Oxides to N-Vinylcarbazole: Regioselective Formation of 5-(9-Carbazolyl)-δ2-isoxazolines.;ChemInform;1989-08-15
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