SYNTHESIS OF BENZANELLATED CARBACEPHAMES .2.

被引：4

作者：

SCHWENNINGER, R ^{[1
]}

ONGANIA, KH ^{[1
]}

机构：

[1] UNIV INNSBRUCK, INST ORGAN CHEM, A-6020 INNSBRUCK, AUSTRIA

来源：

MONATSHEFTE FUR CHEMIE | 1995年 / 126卷 / 02期

关键词：

CARBACEPHAME; CARBACEPHEME, 2,2A-DIHYDRO-AZETO[1,2-A]QUINOLINE-1-ONE; 2-(2-OXO-1-AZETIDINYL)-BENZYLTRIPHENYLPHOPHONIUM SALT; 3-ALKOXYQUINOLINES;

D O I：

10.1007/BF00812247

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The treatment of 2-(oxo-1-azetidinyl)-benzyltriphenylphosphponium salts 9 and 13b, c, d, and e with base leads to carbacephemes 10 and 14b, c, d, and e which can be reduced to the title compounds. The reaction of 14 with acids does not result in 3-oxocephames by cleavage of the enolether function. Instead, the 3-alkoxyquinolines 15b and c have been obtained.

引用

页码：187 / 199

页数：13

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