C-6和C-9取代的3-氮杂双环[3.3.1]壬烷的1H和13C核磁共振谱。

1H and 13C NMR spectra of C-6 and C-9 substituted 3-azabicyclco[3.3.1]nonanes.

作者信息

Goodall Kirsten, Brimble Margaret, Barker David

机构信息

Department of Chemistry, University of Auckland, Auckland, New Zealand.

出版信息

Magn Reson Chem. 2008 Jan;46(1):75-9. doi: 10.1002/mrc.2100.

DOI:10.1002/mrc.2100

PMID:18041010

Abstract

The 1H and 13C NMR data for 3-azabicyclo[3.3.1]nonanes with OH and OMe substituents at C-6 and C-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.

摘要

使用一维（DEPT）和二维（COSY、HSQC、HMBC、NOESY）实验测量了在C-6和C-9处带有OH和OMe取代基的3-氮杂双环[3.3.1]壬烷的1H和13C NMR数据。这些NMR数据的比较说明了这些位置的立体化学和取代的影响。