THE CYCLOADDITION OF 2-PHENYLAMINO-1-AZAAZULENE WITH DIPHENYLACETYLENE USING PALLADIUM CATALYTIC SYSTEMS

Selective cycloaddition was achieved by the reaction of 2-phehylamino-1-azaazulene (3) with diphenylacetylene (4) in the presence of Pd catalyst providing N-(1-azaazulen-2-yl)-2,3-diphenylindoles.

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Bibliographic Details
Published inHeterocycles Vol. 90; no. 1; pp. 715 - 722
Main Authors Fujii, Hiroyuki, Oka, Shigeki, Nakamura, Ippei, Kawai, Yu, Ikeda, Reiko, Konakahara, Takeo, Abe, Noritaka
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier 01.01.2015
Subjects
Chemistry
Chemistry, Organic
Physical Sciences
Science & Technology
CHEMISTRY
CYTOTOXIC ACTIVITY
HETEROARYLAMINATION
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Summary:Selective cycloaddition was achieved by the reaction of 2-phehylamino-1-azaazulene (3) with diphenylacetylene (4) in the presence of Pd catalyst providing N-(1-azaazulen-2-yl)-2,3-diphenylindoles.
ISSN:0385-5414
1881-0942
DOI:10.3987/COM-14-S(K)50