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Structure of a norbornane‐fused pentacyclic isoxazoline
Author(s) -
Sohár Pál,
Kövesdi István,
FrimpongManso Samuel,
Stájer Géza,
Bernáth Gábor
Publication year - 1990
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.1260281205
Subject(s) - chemistry , norbornane , nuclear overhauser effect , adduct , steric effects , nuclear magnetic resonance spectroscopy , stereochemistry , two dimensional nuclear magnetic resonance spectroscopy , organic chemistry
The steric structure of a pentacyclic adduct formed as a by‐product in a retro‐Diels‐Alder reaction was elucidated by 1 H and 13 C NMR spectroscopy, making use of double resonance and differential nuclear Overhauser effect measurements.

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