亚胺离子
试剂
烷基
钯
芳基
化学
催化作用
药物化学
组合化学
有机化学
作者
Hirokazu Tsukamoto,Yoshinori Kondo
标识
DOI:10.1002/anie.200800823
摘要
The biologically important title heterocyclic compounds can be synthesized by two methods based on the cyclization of alkynyl and allenyl iminium ions generated in situ in the presence of organometallic reagents (see scheme). Symmetrical and unsymmetrical tetrahydropyridines with diverse substituents R4 were prepared in a single step under mild conditions. R1=n-, sec-, tert-alkyl; R4=aryl, 1-alkenyl, alkyl, 1-alkynyl, B(pinacolato). Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2008/z800823_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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