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Structure of norbornene‐fused 3,1‐oxazine double cycloadducts
Author(s) -
Sohár Pál,
Bernáth Gábor,
Stájer Géza,
Szabo Angela E.
Publication year - 1989
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.1260270910
Subject(s) - chemistry , norbornene , benzonitrile , oxazines , cycloaddition , nuclear magnetic resonance spectroscopy , oxide , stereochemistry , computational chemistry , organic chemistry , polymer , catalysis , monomer
Pentacyclic isoxazolines were obtained by the cycloaddition of benzonitrile oxide to norbornene‐azetidinone‐fused 3,1‐oxazines. The constitutions of two of the isomers obtained, and the configurations and conformations of all products, were determined by means of 1 H and 13 C NMR spectroscopy and DNOE experiments.

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