Addition of methanol to -tricyclo[3.2.1.02,4]oct-6-ene: a probe of cyclopropyl corner edge protonation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Novel regiospecificity in the acid-catalyzed addition of acetic acid to -tricyclo[3.2.1.02,4]oct-6-ene
2. M.A. Battiste and J.M. Coxon, unpublished data.
3. Stereochemistry of cyclopropane ring opening in the acid-catalyzed fragmentation of -8-tricyclo[3.2.1.02,4]octanone
4. Nucleophilic step of ring-opening reactions of cyclopropanes with electrophiles. Electronic substituent effects on stereoselectivity of reactions of some 1-arylbicyclo[4.1.0]heptanes with mercuric salts
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. Amide-Group-Directed Protonolysis of Cyclopropane: An Approach to 2,2-Disubstituted Pyrrolidines;Organic Letters;2017-04-28
2. Corrigendum:Se-Phenyl Prop-2-eneselenoate: An Ethylene Equivalent for Diels-Alder Reactions;Angewandte Chemie International Edition;2013-11-08
3. Berichtigung:Se-Phenyl Prop-2-eneselenoate: An Ethylene Equivalent for Diels-Alder Reactions;Angewandte Chemie;2013-11-08
4. ChemInform Abstract: ADDITION OF METHANOL TO ENDO-TRICYCLO(3.2.1.02,4)OCT-6-ENE: A PROBE OF CYCLOPROPYL CORNER VS. EDGE PROTONATION;Chemischer Informationsdienst;1983-05-17
5. Reaction of tetracyclo[3.3.0.02,4.03,6]oct-7-ene with HCL and DCL; successive formation of edge- and corner-protonated cyclopropanes;Tetrahedron Letters;1983-01
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