Photochemical reactions of quinoid α-aryl-substituted γ-oxo-α,β-unsaturated carboxylic esters and amides. Formation of naphthacene and cycloheptatriene derivatives
Author:
Funder
Netherlands Foundation of Chemical Research
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/recl.19821010203/fullpdf
Reference42 articles.
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2. Preparation and photochemical electrocyclic reactions of quinoid γ-oxo-α,β-unsaturated esters. Rearrangements to α-alkoxy-γ-lactones
3. Boron trifluoride catalysed rearrangement and decarbonylation of quinoid γ-oxo-α,β-unsaturated thiolesters. α-Alkylthio-γ-lactones
4. Formation of γ-lactones by boron trifluoride-catalysed ring closure of quinoid γ-oxo-α,β-unsaturated carboxamides. Structure and reaction mechanism
5. Photoaddition of phenanthraquinone to alkyl-substituted (alkylthio)acetylenes. Chemistry of acetylenic ethers 109
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1. Reactions of cisoid α-methoxyimino ketones with N,N-diethyl-1-propyn-1-amine. Formation of a γ-methoxyimino α,β-unsaturated carboxamide or a 1,4-benzoxazine;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Photochemical reactions. 137th communication. Preparation and photolysis of (E/Z)-7-methyl-?-ionone;Helvetica Chimica Acta;1984-08-08
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