Bromination of endo-7-norbornene derivatives revisited: failure of a computational NMR method in elucidating the configuration of an organic structure

Bromination of endo-7-norbornene derivatives revisited: failure of a computational NMR method in elucidating the configuration of an organic structure

Previously we reported on the bromination of endo-7-bromonorbornene at different temperatures yielding mixtures of addition products. The structural elucidations of the formed compounds were achieved by NMR spectroscopy. Particularly, the γ-gauche effect and long-range couplings were instrumental in...

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Bibliographic Details
Main Authors: Demet Demirci Gültekin, Arif Daştan, Yavuz Taşkesenligil, Cavit Kazaz, Yunus Zorlu, Metin Balci
Format: Article
Language:English
Published: Beilstein-Institut 2023-06-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
bromination
computational nmr
γ-gauche effect
nmr
noe-diff experiments
Online Access:https://doi.org/10.3762/bjoc.19.56

Internet

https://doi.org/10.3762/bjoc.19.56

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