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Synthesis of 3-alkyl spiro[4,5]trienones by copper-catalyzed oxidative ipso-annulation of activated alkynes with unactivated alkanes.
Chem Commun (Camb). 2016 Feb 11; 52(12):2573-6.CC

Abstract

A Cu-catalyzed oxidative ipso-annulation of activated alkynes with unactivated alkanes for the synthesis of 3-alkyl spiro[4,5]trienones is described. This method allows the formation of two carbon-carbon bonds and one carbon-oxygen bond in a single reaction through a sequence of C-H oxidative coupling, ipso-carbocyclization and dearomatization.

Authors+Show Affiliations

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China. srj0731@hnu.edu.cn jhli@hnu.edu.cn.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

26744747

Citation

Ouyang, Xuan-Hui, et al. "Synthesis of 3-alkyl Spiro[4,5]trienones By Copper-catalyzed Oxidative Ipso-annulation of Activated Alkynes With Unactivated Alkanes." Chemical Communications (Cambridge, England), vol. 52, no. 12, 2016, pp. 2573-6.
Ouyang XH, Song RJ, Liu B, et al. Synthesis of 3-alkyl spiro[4,5]trienones by copper-catalyzed oxidative ipso-annulation of activated alkynes with unactivated alkanes. Chem Commun (Camb). 2016;52(12):2573-6.
Ouyang, X. H., Song, R. J., Liu, B., & Li, J. H. (2016). Synthesis of 3-alkyl spiro[4,5]trienones by copper-catalyzed oxidative ipso-annulation of activated alkynes with unactivated alkanes. Chemical Communications (Cambridge, England), 52(12), 2573-6. https://doi.org/10.1039/c5cc08952b
Ouyang XH, et al. Synthesis of 3-alkyl Spiro[4,5]trienones By Copper-catalyzed Oxidative Ipso-annulation of Activated Alkynes With Unactivated Alkanes. Chem Commun (Camb). 2016 Feb 11;52(12):2573-6. PubMed PMID: 26744747.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Synthesis of 3-alkyl spiro[4,5]trienones by copper-catalyzed oxidative ipso-annulation of activated alkynes with unactivated alkanes. AU - Ouyang,Xuan-Hui, AU - Song,Ren-Jie, AU - Liu,Bang, AU - Li,Jin-Heng, Y1 - 2016/01/08/ PY - 2016/1/9/entrez PY - 2016/1/9/pubmed PY - 2016/1/9/medline SP - 2573 EP - 6 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) VL - 52 IS - 12 N2 - A Cu-catalyzed oxidative ipso-annulation of activated alkynes with unactivated alkanes for the synthesis of 3-alkyl spiro[4,5]trienones is described. This method allows the formation of two carbon-carbon bonds and one carbon-oxygen bond in a single reaction through a sequence of C-H oxidative coupling, ipso-carbocyclization and dearomatization. SN - 1364-548X UR - https://www.unboundmedicine.com/medline/citation/26744747/Synthesis_of_3_alkyl_spiro[45]trienones_by_copper_catalyzed_oxidative_ipso_annulation_of_activated_alkynes_with_unactivated_alkanes_ DB - PRIME DP - Unbound Medicine ER -
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