Simple and condensed β-lactams -: Part 31.: Acid catalyzed ring closures and ring transformations of some 3-aryloxy-4-oxoazetidin-2-carbaldehydes

被引:12
作者
Bertha, F
Fetter, J [1 ]
Kajtár-Peredy, M
Lempert, K
Czira, G
机构
[1] Tech Univ Budapest, Dept Organ Chem, H-1521 Budapest, Hungary
[2] Hungarian Acad Sci, Chem Res Ctr, Inst Chem, H-1525 Budapest, Hungary
[3] Gedeon Richter Chem Works Ltd, H-1475 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
azetidinones; chromenes; diastereoselection; ring transformations;
D O I
10.1016/S0040-4020(98)00951-X
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Carbaldehydes 1a and 1b, when treated with Lewis or Bronsted acids in non-aromatic solvents or in nitrobenzene afford dihydrochromeno[3,2-b]azet-2(1H)-ones of types 4-6 and 10. In toluene, chloro- and fluoro-benzene related compounds of types 7-9 were obtained, in the last named two solvents accompanied by pyrrolidin-2-one derivatives 11-15. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:15227 / 15242
页数:16
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