CHEMISTRY OF PYRIDINE .7. TETRAHYDROPYRIDINES FROM REACTION OF PYRIDINE N-OXIDES WITH MERCAPTANS IN ACETIC ANHYDRIDE

被引:20
作者
HERSHENS.FM
BAUER, L
机构
[1] Department of Chemistry, College of Pharmacy, University of Illinois at the Medical Center, Chicago
关键词
D O I
10.1021/jo01255a039
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A number of solids isolated from the reaction of pyridine N-oxides with mercaptans in acetic anhydride were shown to be 1-acetyl-1,2,3,6-tetrahydropyridines. One feature common to these compounds was that a sulfide group was attached to the β sp3 ring carbon while both the α positions on the ring were substituted by either sulfide or acetoxy groups. The formation of these products is discussed in terms of the episulfonium intermediate proposed in the prior paper. © 1969, American Chemical Society. All rights reserved.
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页码:660 / &
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