A convenient and efficient route for the allylation of aromatic amines and α-aryl aldehydes with alkynes in the presence of a Pd(0)TPhCOOH combined catalyst system

Nitin T. Patil, Huanyou Wu, Isao Kadota, Yoshinori Yamamoto

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

The allylation of aromatic amines with alkynes proceeded smoothly in the presence of catalytic amounts of Pd(PPh3)4 and benzoic acid. The allylation products were obtained in high yields in a regio- and stereoselective manner. The effect of various groups on the nitrogen atom of anilines was studied. Regardless of the substituent (electron withdrawing or electron donating) on the aromatic ring, the reaction proceeded well. Various functionalities, including -CH3, -OMe, -Cl, -CN, -COOMe, -NO 2 and -COCH3 were tolerated under the reaction conditions. Similarly, the allylation of α-aryl aldehydes proceeded well with the same level of regio- and stereoselectivity as the allylation of aromatic amines. This reaction provides the second example of the transition metal catalyzed direct α-allylation of aldehydes.

Original languageEnglish
Pages (from-to)8745-8750
Number of pages6
JournalJournal of Organic Chemistry
Volume69
Issue number25
DOIs
Publication statusPublished - Dec 10 2004
Externally publishedYes

ASJC Scopus subject areas

  • Organic Chemistry

Fingerprint Dive into the research topics of 'A convenient and efficient route for the allylation of aromatic amines and α-aryl aldehydes with alkynes in the presence of a Pd(0)TPhCOOH combined catalyst system'. Together they form a unique fingerprint.

  • Cite this