Preparation of novel selenapenams and selenacephems by nucleophilic and radical chemistry involving benzyl selenides

被引：28

作者：

Carland, MW ^{[1
]}

Martin, RL ^{[1
]}

Schiesser, CH ^{[1
]}

机构：

[1] Univ Melbourne, Sch Chem, Bio21 Mol Sci & Biotechnol Inst, Melbourne, Vic 3010, Australia

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2004年 / 2卷 / 18期

关键词：

D O I：

10.1039/b409242b

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

2,2a-Dihydro-1H, 8H-azeto[2,1-b][1,3] benzoselenazin-1-one (12), 5-selena-1-azabicyclo[4.2.0] oct-3-en-8-one (13), ethyl 1-aza-7-oxo-4-selenabicyclo[3.2.0] heptane-2-carboxylate (16), and benzoselenopenem (33) can be prepared in 39 - 85% yield through the intramolecular homolytic substitution of aryl, vinyl or alkyl radicals at the selenium atom in suitably-substituted 4-benzylseleno-beta-lactams, or through intramolecular nucleophilic substitution by the benzylseleno moiety in 4-halo-beta-lactam precursors. Application of this chemistry to the preparation of optically active selenium-containing analogues of beta-lactam antibiotics is also detailed.

引用

页码：2612 / 2618

页数：7

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