2-(Azidomethyl)phenylboronic acid in the synthesis of isoquinoline derivatives

被引：0
|
作者：
O. G. Ganina
S. G. Zamotaeva
M. A. Nosarev
O. V. Kosenkova
M. I. Naumov
A. S. Shavyrin
J.-P. Finet
A. Yu. Fedorov
机构：
[1] N. I. Lobachevsky Nizhnii Novgorod State University,Department of Chemistry
[2] M. V. Lomonosov Moscow State University,G. A. Razuvaev Institute of Organometallic Chemistry
[3] Russian Academy of Sciences,undefined
[4] UMR-CNRS 6517,undefined
[5] Universites d'Aix-Marseille 1 et 3,undefined
[6] Faculte des Sciences Saint-Jerome,undefined
来源：
Russian Chemical Bulletin | 2005年 / 54卷
关键词：
2-(azidomethyl)phenylboronic acid; organolead compounds; isoquinolines; isochromanes; α-arylation; reductive coupling; lead tetraacetate;
D O I：
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中图分类号：
学科分类号：
摘要：
2-(Azidomethyl)phenyllead triacetate was obtained by the reaction of 2-(azidomethyl)phenylboronic acid with lead tetraacetate. A strategy for the synthesis of isoquinoline derivatives was proposed that involves a reaction of this organolead reagent with enolizable substrates followed by annelation in the presence of triphenylphosphine. The use of 2-(azidomethyl)phenylboronic acid allowed α-arylation products to be obtained from β-diketones and natural β-oxo lactones in good yields.
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页码：1606 / 1611
页数：5
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