First synthesis of caerulomycin B.: A new synthesis of caerulomycin C

被引:54
作者
Mongin, F [1 ]
Trécourt, F [1 ]
Gervais, B [1 ]
Mongin, O [1 ]
Quéguiner, G [1 ]
机构
[1] IRCOF, UMR 6014, Lab Chim Organ Fine & Heterocycl, F-76131 Mont St Aignan, France
关键词
D O I
10.1021/jo010913r
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Caerulomycins produced by Streptomyces caeruleus are bipyridinic molecules endowed with antibiotic properties. The first synthesis of caerulomycin B (1) as well as a new synthesis of caerulomycin C (2) are reported. Starting from 3-hydroxypyridine, the same methodology was used to prepare both compounds 1 and 2. Efficiently controlled reactions such as metalation to allow the synthesis of 2,6-diiodo-3,4-dialkoxypyridines, which are key intermediates, and further halogen lithium exchange and cross-coupling to reach the targets molecules 1 and 2 have been developed.
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页码:3272 / 3276
页数:5
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