Sequential ruthenium-catalyzed hydroamination and rhenium-catalyzed C-H bond activation leading to indene derivatives

Yoichiro Kuninobu; Yuta Nishina; Kazuhiko Takai

doi:10.1021/ol0611292

Sequential ruthenium-catalyzed hydroamination and rhenium-catalyzed C-H bond activation leading to indene derivatives

Yoichiro Kuninobu
, Yuta Nishina
, Kazuhiko Takai

Research output: Contribution to journal › Article › peer-review

43 Citations (Scopus)

Abstract

Formal [3+2] annulation of arylacetylenes and α,β-unsaturated carbonyl compounds is achieved in a one-pot reaction by successive treatment of the acetylenes with aniline and a catalytic amount of Ru₃(CO) ₁₂ and NH₄PF₆ and C-H bond activation catalyzed by [ReBr(CO)₃(thf)]₂. The result suggests that the second rhenium-catalyzed indene formation is not disturbed by the first catalyst system.

Original language	English
Pages (from-to)	2891-2893
Number of pages	3
Journal	Organic letters
Volume	8
Issue number	13
DOIs	https://doi.org/10.1021/ol0611292
Publication status	Published - Jun 22 2006
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol0611292

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abstract = "Formal [3+2] annulation of arylacetylenes and α,β-unsaturated carbonyl compounds is achieved in a one-pot reaction by successive treatment of the acetylenes with aniline and a catalytic amount of Ru3(CO) 12 and NH4PF6 and C-H bond activation catalyzed by [ReBr(CO)3(thf)]2. The result suggests that the second rhenium-catalyzed indene formation is not disturbed by the first catalyst system.",

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AU - Kuninobu, Yoichiro

AU - Nishina, Yuta

AU - Takai, Kazuhiko

PY - 2006/6/22

Y1 - 2006/6/22

N2 - Formal [3+2] annulation of arylacetylenes and α,β-unsaturated carbonyl compounds is achieved in a one-pot reaction by successive treatment of the acetylenes with aniline and a catalytic amount of Ru3(CO) 12 and NH4PF6 and C-H bond activation catalyzed by [ReBr(CO)3(thf)]2. The result suggests that the second rhenium-catalyzed indene formation is not disturbed by the first catalyst system.

AB - Formal [3+2] annulation of arylacetylenes and α,β-unsaturated carbonyl compounds is achieved in a one-pot reaction by successive treatment of the acetylenes with aniline and a catalytic amount of Ru3(CO) 12 and NH4PF6 and C-H bond activation catalyzed by [ReBr(CO)3(thf)]2. The result suggests that the second rhenium-catalyzed indene formation is not disturbed by the first catalyst system.

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JF - Organic letters

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Sequential ruthenium-catalyzed hydroamination and rhenium-catalyzed C-H bond activation leading to indene derivatives

Abstract

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