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Stereochemical features of meta photocycloadducts derived from 3-alkyl-4-phenoxybut-1-enes

✍ Scribed by Erik van der Eycken; Denis de Keukeleire; André de Bruyn; Johan van der Eycken; Andrew Gilbert


Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
342 KB
Volume
114
Category
Article
ISSN
0165-0513

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## Abstract ^1^H NMR data (400 and 500 MHz) are reported for the intramolecular __meta__ photocycloaddition products from 4‐phenoxybut‐1‐enes and 3‐benzyloxyprop‐1‐enes. The structures of these photoproducts, and in particular the discrimination between the 1,6‐ and 7,8‐bridged isomers, are deduced

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