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Highly chemoselective nickel-catalyzed three-component cross-trimerization between two distinct terminal alkynes and an internal alkyne.
Org Lett. 2011 Jan 07; 13(1):122-5.OL

Abstract

The highly chemo-, regio-, and stereoselective three-component cross-trimerization reaction between triisopropylsilylacetylene, diarylacetylene, and a terminal alkyne was achieved by Ni(cod)(2)/P(p-CF(3)C(6)H(4))(3) catalyst at room temperature via selective C-H oxidative addition of the terminal silylacetylene. The reaction is applicable for various diarylacetylenes and terminal alkynes to yield the corresponding 1,3-diene-5-yne compounds.

Authors+Show Affiliations

Department of Applied Chemistry, Institute of Science and Enginnering, Chuo University, 1-13-27 Kasuga, Bunkyo-ku, Tokyo 112-8551, Japan. kogata@kc.chuo-u.ac.jpNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

21133396

Citation

Ogata, Kenichi, et al. "Highly Chemoselective Nickel-catalyzed Three-component Cross-trimerization Between Two Distinct Terminal Alkynes and an Internal Alkyne." Organic Letters, vol. 13, no. 1, 2011, pp. 122-5.
Ogata K, Atsuumi Y, Fukuzawa S. Highly chemoselective nickel-catalyzed three-component cross-trimerization between two distinct terminal alkynes and an internal alkyne. Org Lett. 2011;13(1):122-5.
Ogata, K., Atsuumi, Y., & Fukuzawa, S. (2011). Highly chemoselective nickel-catalyzed three-component cross-trimerization between two distinct terminal alkynes and an internal alkyne. Organic Letters, 13(1), 122-5. https://doi.org/10.1021/ol102687p
Ogata K, Atsuumi Y, Fukuzawa S. Highly Chemoselective Nickel-catalyzed Three-component Cross-trimerization Between Two Distinct Terminal Alkynes and an Internal Alkyne. Org Lett. 2011 Jan 7;13(1):122-5. PubMed PMID: 21133396.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Highly chemoselective nickel-catalyzed three-component cross-trimerization between two distinct terminal alkynes and an internal alkyne. AU - Ogata,Kenichi, AU - Atsuumi,Yuka, AU - Fukuzawa,Shin-Ichi, Y1 - 2010/12/06/ PY - 2010/12/8/entrez PY - 2010/12/8/pubmed PY - 2010/12/8/medline SP - 122 EP - 5 JF - Organic letters JO - Org Lett VL - 13 IS - 1 N2 - The highly chemo-, regio-, and stereoselective three-component cross-trimerization reaction between triisopropylsilylacetylene, diarylacetylene, and a terminal alkyne was achieved by Ni(cod)(2)/P(p-CF(3)C(6)H(4))(3) catalyst at room temperature via selective C-H oxidative addition of the terminal silylacetylene. The reaction is applicable for various diarylacetylenes and terminal alkynes to yield the corresponding 1,3-diene-5-yne compounds. SN - 1523-7052 UR - https://www.unboundmedicine.com/medline/citation/21133396/Highly_chemoselective_nickel_catalyzed_three_component_cross_trimerization_between_two_distinct_terminal_alkynes_and_an_internal_alkyne_ L2 - https://doi.org/10.1021/ol102687p DB - PRIME DP - Unbound Medicine ER -
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