The high-Ðeld 1H NMR analysis of 3-substituted camphors with OH, OMe, SMe, NHMe, and Me substit-NMe 2 uents at endo and exo positions, and also with an oxo substituent, is reported. The substituent-induced chemical shifts (SCS) obtained for these difunctional systems, including those from previous w
Substituent effects on 1H chemical shifts. I—complete 1H chemical shift assignments of methyl-substituted cyclic systems
✍ Scribed by Julie Fisher; Michael J. Gradwell
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 655 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^1^H chemical shift assignments are presented for 2‐methyladamantane, 2‐methylnorbornane (endo and exo) and 2‐methylnorbornene (endo and exo). Resonance assignment was achieved using a variety of 1D and 2D homo‐ and heteronuclear (^1^H–^13^C) experiments. The methyl group‐induced substituent chemical shift (SCS) is derived and the SCS of protons vicinal to this group is discussed.
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