Synthese und seitenselektive Diels‐Alder‐Reaktion von Homodehydroisodicyclopentadien
Author:
Affiliation:
1. Institut für Organische Chemie der Justus‐Liebig‐Universität, Heinrich‐Buff‐Ring 58, D‐6300 Gießen
2. Institut für Anorganische Chemie der Universität, Universitätsstraße 5–7, D‐4300 Essen
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19901230215
Reference36 articles.
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4. .pi.-Facial selectivity in Diels-Alder reactions of hexacyclo[10.2.1.02,11.04,9.04,14.09,13]pentadeca-5,7-diene-3,10-dione
5. Modeling of steric control of facial stereoselectivity. Diels-Alder cycloadditions of unsymmetrically substituted cyclopentadienes
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1. Electronic Structure of Diene and Polyene Radical Cations;PATAI'S Chemistry of Functional Groups;2009-12-15
2. Face selectivity of theDiels-Alder additions and cheletropic additions of sulfur dioxide to 2- vinyl-7-oxabicyclo[2.2.1]hept-2-ene derivatives;Helvetica Chimica Acta;1994-05-11
3. Enantiomerically pure cyclopentadienes;Chemical Reviews;1993-03-01
4. Generation and interception of isodicyclopentadiene tautomers by diene transmissive Diels-Alder reaction of a 1,5-dihydropentalene with a variety of dienophiles;The Journal of Organic Chemistry;1992-07
5. π-Facial stereoselectivity in the Diels–Alder reactions of a rigid carbocyclic diene: spiro(bicyclo[2.2.1]heptane-2,1′-[2,4]cyclopentadiene);Canadian Journal of Chemistry;1991-01-01
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