COMPOUNDS WITH BRIDGEHEAD NITROGEN .62. NMR-SPECTRA AND STEREOCHEMISTRY OF PERHYDROPYRIDO[1,2-C][1,3]THIAZEPINES AND RELATED SYSTEMS

被引:2
|
作者
CRABB, TA
FALLAH, A
机构
[1] Department of Chemistry, Portsmouth Polytechnic, Portsmouth, Hampshire
关键词
!sup]1[!/sup]H and [!sup]13[!/sup]C NMR; Perhydropyrido[1,2‐c][1,3]thiazepines;
D O I
10.1002/mrc.1260280509
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Perhydropyrido[1,2‐c][1,3] thiazepine adopts (CDCl3 solution, 25°C) an equilibrium containing > 98% trans‐fused conformer, in contrast to perhydropyrido[1,2‐c][1,3]oxazepine, which adopts a ca. 74% trans‐fused ⇌ 26% O‐inside‐cis‐fused conformational equilibrium. The cis‐(H‐5a, H‐8)‐8‐ethyl‐substituted derivatives of both systems show increased preference for the S/O inside cis conformations. The related 2‐tert‐butylperhydropyrido[1,2‐c][1,3]diazepine adopts predominantly the trans‐fused conformation. Copyright © 1990 John Wiley & Sons, Ltd.
引用
收藏
页码:426 / 430
页数:5
相关论文
共 50 条