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.
Links
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 -