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NMR study of complex triquinanes and bulleranes derived from photoisomerization of aryl‐substituted norbornan‐2‐ones
Author(s) -
De Keukeleire Denis,
He ShuLin,
De Bruyn André
Publication year - 1992
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/mrc.1260301305
Subject(s) - chemistry , photoisomerization , alkene , intramolecular force , aryl , carbon 13 nmr , molecule , proton nmr , stereochemistry , computational chemistry , isomerization , organic chemistry , alkyl , catalysis
Analysis of 1 H and 13 C NMR data by 2D NMR techniques was used for the structural identification of triquinanes and bulleranes considered as precursors of complex natural products such as (+)‐cerapicol. The polycyclic molecules are derived from a tandem Norrish Type I photoreaction and intramolecular arene–alkene meta photocycloaddition of aryl‐substituted norbornan‐2‐ones.
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