Miyake T, Koyama Y
Institute of Bioorganic Chemistry, Kawasaki, Japan.
Carbohydr Res. 1994 May 20;258:11-26. doi: 10.1016/0008-6215(94)84071-7.
5-Deoxy-5-fluoroarbekacin (1) and 5-deoxy-5,5-difluoroarbekacin (2) showed interunit, through-space 1H-19F spin-spin couplings at the signals for H-1', 4", 5", 6"a and 6"b with F-5eq. These couplings were detected by a new NMR method, 1H-detected 2D 1H-19F chemical shift correlation spectroscopy. These two compounds also displayed interunit, through-space 13C-19F couplings at the resonances for C-1' and 5" with F-5eq. These couplings were corroborated by 1D 13C[1H]-[19F] triple-resonance techniques. Triple-resonance 13C-19F COSY experiments were also carried out. The interunit conformational information obtained with the through-space 1H-19F and 13C-19F couplings was further supported by heteronuclear 1H[19F] NOE experiments.
5-脱氧-5-氟阿贝卡星(1)和5-脱氧-5,5-二氟阿贝卡星(2)在H-1'、4"、5"、6"a和6"b与F-5eq的信号处显示出单元间的空间1H-19F自旋-自旋耦合。这些耦合通过一种新的核磁共振方法——1H检测的二维1H-19F化学位移相关光谱法检测到。这两种化合物在C-1'和5"与F-5eq的共振处也显示出单元间的空间13C-19F耦合。这些耦合通过一维13C[1H]-[19F]三共振技术得到证实。还进行了三共振13C-19F COSY实验。通过空间1H-19F和13C-19F耦合获得的单元间构象信息通过异核1H[19F] NOE实验得到进一步支持。