Chelation-assisted hydrative dimerization of 1-alkyne forming α,β-enones by an Rh(I) catalyst

Jun Park Young; Bong Il Kwon; Jeong Ae Ahn; Hyuk Lee; Chul Ho Jun

doi:10.1021/ja045789i

Chelation-assisted hydrative dimerization of 1-alkyne forming α,β-enones by an Rh(I) catalyst

Jun Park Young, Bong Il Kwon, Jeong Ae Ahn, Hyuk Lee, Chul Ho Jun

Department of Chemistry

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

38 Citations (Scopus)

Abstract

The intermolecular hydrative dimerization of 1-alkyne was developed through the chelation-assisted catalytic system with Rh(I)/2-amino-3-picoline. This novel transformation afforded branched and linear α,β-enones directly from two 1-alkyne molecules and H₂O. The results demonstrate that a branch/linear ratio can be controlled by the alkyl substituent of 1-alkyne.

Original language	English
Pages (from-to)	13892-13893
Number of pages	2
Journal	Journal of the American Chemical Society
Volume	126
Issue number	43
DOIs	https://doi.org/10.1021/ja045789i
Publication status	Published - 2004 Nov 3

All Science Journal Classification (ASJC) codes

Catalysis
Chemistry(all)
Biochemistry
Colloid and Surface Chemistry

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10.1021/ja045789i

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abstract = "The intermolecular hydrative dimerization of 1-alkyne was developed through the chelation-assisted catalytic system with Rh(I)/2-amino-3-picoline. This novel transformation afforded branched and linear α,β-enones directly from two 1-alkyne molecules and H2O. The results demonstrate that a branch/linear ratio can be controlled by the alkyl substituent of 1-alkyne.",

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AU - Young, Jun Park

AU - Kwon, Bong Il

AU - Ahn, Jeong Ae

AU - Lee, Hyuk

AU - Jun, Chul Ho

PY - 2004/11/3

Y1 - 2004/11/3

N2 - The intermolecular hydrative dimerization of 1-alkyne was developed through the chelation-assisted catalytic system with Rh(I)/2-amino-3-picoline. This novel transformation afforded branched and linear α,β-enones directly from two 1-alkyne molecules and H2O. The results demonstrate that a branch/linear ratio can be controlled by the alkyl substituent of 1-alkyne.

AB - The intermolecular hydrative dimerization of 1-alkyne was developed through the chelation-assisted catalytic system with Rh(I)/2-amino-3-picoline. This novel transformation afforded branched and linear α,β-enones directly from two 1-alkyne molecules and H2O. The results demonstrate that a branch/linear ratio can be controlled by the alkyl substituent of 1-alkyne.

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Chelation-assisted hydrative dimerization of 1-alkyne forming α,β-enones by an Rh(I) catalyst

Abstract

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