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A chemo- and regioselective Pd(0)-catalyzed three-component spiroannulation.
Chem Commun (Camb). 2021 Jan 28; 57(9):1117-1120.CC

Abstract

A chemo- and regioselective Pd(0)-catalyzed spiroannulation has been successfully developed. The key feature of this method is the use of readily available 1,2-dihaloarenes, alkynes and 2-naphthols for the rapid assembly of spirocarbocyclic molecules. Mechanistic studies revealed that this domino reaction proceeded through a cascade of oxidative addition to Pd(0), alkyne migratory insertion, and 2-naphthol-facilitated dearomatizing [4+1] spiroannulation.

Authors+Show Affiliations

Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an 710127, China. xluan@nwu.edu.cn bailu@nwu.edu.cn.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

33410450

Citation

Wu, Jiaoyu, et al. "A Chemo- and Regioselective Pd(0)-catalyzed Three-component Spiroannulation." Chemical Communications (Cambridge, England), vol. 57, no. 9, 2021, pp. 1117-1120.
Wu J, Bai L, Han L, et al. A chemo- and regioselective Pd(0)-catalyzed three-component spiroannulation. Chem Commun (Camb). 2021;57(9):1117-1120.
Wu, J., Bai, L., Han, L., Liu, J., & Luan, X. (2021). A chemo- and regioselective Pd(0)-catalyzed three-component spiroannulation. Chemical Communications (Cambridge, England), 57(9), 1117-1120. https://doi.org/10.1039/d0cc07389j
Wu J, et al. A Chemo- and Regioselective Pd(0)-catalyzed Three-component Spiroannulation. Chem Commun (Camb). 2021 Jan 28;57(9):1117-1120. PubMed PMID: 33410450.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A chemo- and regioselective Pd(0)-catalyzed three-component spiroannulation. AU - Wu,Jiaoyu, AU - Bai,Lu, AU - Han,Lingbo, AU - Liu,Jingjing, AU - Luan,Xinjun, Y1 - 2021/01/07/ PY - 2021/1/8/pubmed PY - 2021/1/8/medline PY - 2021/1/7/entrez SP - 1117 EP - 1120 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) VL - 57 IS - 9 N2 - A chemo- and regioselective Pd(0)-catalyzed spiroannulation has been successfully developed. The key feature of this method is the use of readily available 1,2-dihaloarenes, alkynes and 2-naphthols for the rapid assembly of spirocarbocyclic molecules. Mechanistic studies revealed that this domino reaction proceeded through a cascade of oxidative addition to Pd(0), alkyne migratory insertion, and 2-naphthol-facilitated dearomatizing [4+1] spiroannulation. SN - 1364-548X UR - https://www.unboundmedicine.com/medline/citation/33410450/A_chemo__and_regioselective_Pd_0__catalyzed_three_component_spiroannulation_ DB - PRIME DP - Unbound Medicine ER -
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