Diels-Alder reactions of 5,6-dihydro-2(1H)-pyridones. Preparation of partially reduced cis-isoquinolones and cis-3,4-disubstituted piperidines

被引：8

作者：

Casamitjana, N ^{[1
]}

Jorge, A ^{[1
]}

Perez, CG ^{[1
]}

Bosch, J ^{[1
]}

Espinosa, E ^{[1
]}

Molins, E ^{[1
]}

机构：

[1] CSIC,INST CIENCIA MAT,CERDANYOLA 08193,SPAIN

来源：

TETRAHEDRON LETTERS | 1997年 / 38卷 / 13期

关键词：

D O I：

10.1016/S0040-4039(97)00280-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Diels-Alder reactions of 5,6-dihydro-2(1H)-pyridones with a variety of diversely substituted butadienes to give partially reduced isoquinolones is reported. Reductive ozonolysis of the resulting octahydroisoquinolones gave cis-3,4-disubstituted piperidines. (C) 1997 Elsevier Science Ltd.

引用

页码：2295 / 2298

页数：4

共 8 条

[1] A NEW [ABCD -] ABCDE] CYCLOADDITION STRATEGY FOR THE APPROACH TO YOHIMBE ALKALOIDS - STEREOSELECTIVE SYNTHESIS OF (+/-)-3-EPI-ALLO-YOHIMBONE [J].