Azabicyclic Urethane Rearrangements. I. A Novel Route to Substituted Azabicyclo[3.2.1]oct-2-enes.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
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2. π-route to azabicyclics III. The solvolysis of protonated N-chloramines
3. Stereospecific synthesis of azabicyclics
4. 6-Azabicyclo[3.2.1]octanes
5. Nitroxydes—XLVII
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
1. NMR study of 6-azabicyclo[3.2.1 ]octene derivatives, by-products of catharanthine synthesis;J. Chem. Soc., Perkin Trans. 2;1994
2. Azatricycles from substituted pyridines. Synthesis and rearrangement of N-ethoxycarbonyl-2-azatricyclo[4.3.1.03,7]dec-8-enes.;Tetrahedron;1991-09
3. Regioselective Synthesis of 4-, 5-, and 6-Alkyl and Dialkyl 5,6-Dehydroisoquinuclidines from Phenylvinylsulfone Cycloadducts of N-Ethoxycarbonyl-1,2-Dihydropyridines;Synthetic Communications;1990-07
4. 6-Azabicyclo[3.2.1]octane derivatives;Tetrahedron;1983-01
5. Heterodienophiles VII. A novel synthesis of azabicyclics from methylenebisurethane and p-menthadienes by formal 1,3-cycloaddition reactions.;Tetrahedron Letters;1976-08
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