๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

13C NMR spectroscopy of some 3- and 7-substituted bicyclo[3.3.1]nonanes

โœ Scribed by J.A. Peters; J.M. Van Der Toorn; H. Van Bekkum


Publisher
Elsevier Science
Year
1977
Tongue
French
Weight
505 KB
Volume
33
Category
Article
ISSN
0040-4020

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


1H and 13C NMR spectra of C-6 and C-9 su
โœ Kirsten Goodall; Margaret Brimble; David Barker ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 168 KB

## Abstract The ^1^H and ^13^C NMR data for 3โ€azabicyclo[3.3.1]nonanes with OH and OMe substituents at Cโ€6 and Cโ€9 were measured using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Comparison of this NMR data illustrates the effects of stereochemistry and substitution at these positions.

13C NMR chemical shift assignments for s
โœ Nรบria Casamitjana; Josep Bonjoch; Jordi Grร cia; Joan Bosch ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 235 KB

## Abstract The ^13^C NMR spectra of 26 substituted 2โ€azabicyclo[3.3.1]nonanโ€7โ€ones are reported, providing a diagnostic method for the stereochemical elucidation of the relative configuration of these products.

1H and 13C NMR data for C-6 substituted
โœ Kirsten J. Goodall; Margaret A. Brimble; David Barker ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 122 KB

## Abstract The ^1^H and ^13^C NMR spectra of 3โ€azabicyclo[3.3.1]nonanes with various oxygenated substituents at Cโ€6 were assigned using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Close examination of this NMR data details the effects of substitution and stereochemistry at Cโ€6 in these