Catalytic Pauson - Khand-Type Reaction Using Aldehydes as a CO Source

Takanori Shibata; Natsuko Toshida; Kentaro Takagi

doi:10.1021/ol025836g

Catalytic Pauson - Khand-Type Reaction Using Aldehydes as a CO Source

Takanori Shibata^*, Natsuko Toshida, Kentaro Takagi

^*Corresponding author for this work

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

159 Citations (Scopus)

Abstract

(matrix presented) Rhodium complex-catalyzed carbonylative alkene-alkyne coupling proceeds using aldehydes as a CO source. Cinnamaldehyde is the best CO donor, and various cyclopentenones were provided in high isolated yields by a solvent-free system.

Original language	English
Pages (from-to)	1619-1621
Number of pages	3
Journal	Organic Letters
Volume	4
Issue number	9
DOIs	https://doi.org/10.1021/ol025836g
Publication status	Published - 2002 May 2
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol025836g

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title = "Catalytic Pauson - Khand-Type Reaction Using Aldehydes as a CO Source",

abstract = "(matrix presented) Rhodium complex-catalyzed carbonylative alkene-alkyne coupling proceeds using aldehydes as a CO source. Cinnamaldehyde is the best CO donor, and various cyclopentenones were provided in high isolated yields by a solvent-free system.",

author = "Takanori Shibata and Natsuko Toshida and Kentaro Takagi",

year = "2002",

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doi = "10.1021/ol025836g",

language = "English",

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journal = "Organic Letters",

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AU - Shibata, Takanori

AU - Toshida, Natsuko

AU - Takagi, Kentaro

PY - 2002/5/2

Y1 - 2002/5/2

N2 - (matrix presented) Rhodium complex-catalyzed carbonylative alkene-alkyne coupling proceeds using aldehydes as a CO source. Cinnamaldehyde is the best CO donor, and various cyclopentenones were provided in high isolated yields by a solvent-free system.

AB - (matrix presented) Rhodium complex-catalyzed carbonylative alkene-alkyne coupling proceeds using aldehydes as a CO source. Cinnamaldehyde is the best CO donor, and various cyclopentenones were provided in high isolated yields by a solvent-free system.

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U2 - 10.1021/ol025836g

DO - 10.1021/ol025836g

M3 - Article

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SP - 1619

EP - 1621

JO - Organic Letters

JF - Organic Letters

IS - 9

ER -

Catalytic Pauson - Khand-Type Reaction Using Aldehydes as a CO Source

Abstract

ASJC Scopus subject areas

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