Gold-catalyzed tandem reaction of 2-alkynylanilines followed by 1,6-conjugate addition to p-quinone methides: efficient access to unsymmetrical diarylindolylmethanes

  • Jillella, Raveendra
  • Oh, Dong Hwan
  • Oh, Chang Ho
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초록

A simple, mild, efficient and chemoselective catalytic method for the straightforward synthesis of an interesting class of 2-aryl/alkyl-substituted-3-diaryl indolyl methanes in high yield is reported. This atom-efficient method proceeds via a gold-catalyzed one-pot sequential intramolecular hydroamination (C-N bond formation) of 2-alkynylanilines followed by a 1,6-conjugate addition to p-quinonemethides. The p-quinonemethides, which contain aldehyde functional groups, preferentially participate in 1,6-conjugate addition, while the aldehyde functional group remains unreactive.

키워드

CROSS-COUPLING REACTIONSELECTROPHILIC CYCLIZATIONSEQUENTIAL ARYLATIONO-ALKYNYLANILINESTRIARYLMETHANESINDOLESDERIVATIVESALDEHYDESAGENTSBIS(INDOLYL)METHANES
제목
Gold-catalyzed tandem reaction of 2-alkynylanilines followed by 1,6-conjugate addition to p-quinone methides: efficient access to unsymmetrical diarylindolylmethanes
저자
Jillella, RaveendraOh, Dong HwanOh, Chang Ho
DOI
10.1039/c8nj03955k
발행일
2018-10
유형
Article
저널명
New Journal of Chemistry
42
20
페이지
16886 ~ 16890