Synthesis and cycloaddition reaction of 2,3-dimethylene-7-isopropylidenebenzonorborene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Electronic control of stereoselectivity. 3. Stereoselection operative in [4 + 2].pi. cycloadditions to cyclopentadiene rings fused at C2,C3 to bicyclic frameworks
2. Electronic control of stereoselectivity. 4. Effects of neighboring fused bicyclic frameworks on the stereochemical outcome of Diels-Alder cycloadditions to cyclopentadiene rings
3. Stereoselectivity of the Diels-Alder additions of exocyclic dienes grafted onto bicyclo[2.2.n]alkanes
4. Organic photochemistry. 43. Stereoselective addition of singlet oxygen to 7-isopropylidenenorbornene derivatives. Possibility of .pi.-orbital distortion in the homoconjugated system
5. Electronic control of stereoselectivity. 1. Singlet oxygen and related electrophilic additions to aryl-substituted 7-isopropylidenebenzonorbornenes
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