The Effects of Homoconjugated Cyclopropane and Oxirane Rings on theDiels-Alder Reactivity of 2,3-bis (methylidene)norbornane
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Reference75 articles.
1. Interaction between Non-Conjugated Chromophores: 5,6-Dimethylidene-exo-2-norborneol, 5,6-Dimethylidene-exo,exo-2,3-norbornanediol and 5,6-Dimethylidene-2-norbornanone
2. Hyperconjugative Interactions in Bicyclo[2.2.1]heptane Derivatives. Effects on theDiels-Alder Reactivity of the s-cis-Butadiene Group of 2, 3-Dimethylidene-norbornanes
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1. A concise synthesis of the 2,3-dimethylene-1,4-methano-1,2,3,4-tetrahydronaphthalene and its reaction with singlet oxygen;Tetrahedron;1994-01
2. Regioselective Electrophilic Additions of Bicyclo[2.2.n]alk-2-enes Controlled by Remote Epoxide Functions;Helvetica Chimica Acta;1987-11-04
3. Bicyclo[2.2.1]heptanes;Stereochemical Analysis of Alicyclic Compounds by C-13 NMR Spectroscopy;1987
4. Synthesis and Diels-Alder reactivity of 2,3,6,7-tetrakis(methylene)bicyclo[3.2.1]octane;The Journal of Organic Chemistry;1986-06
5. Face Selectivity in theDiels-Alder Additions and Chelotropic Addition of Sulfur Dioxide to 2-(D)Methylidene-3-methylidenebicyclo[2.2.1]heptane;Helvetica Chimica Acta;1985-09-25
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