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[Fe(F(20)TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source.
Chem Commun (Camb). 2010 Oct 07; 46(37):6926-8.CC

Abstract

The syntheses of alkaloids including indoles, indolines, tetrahydroquinolines, dihydroquinazolinones and quinazolinones have been accomplished in moderate to excellent yields via [Fe(F(20)TPP)Cl] catalyzed intramolecular C-N bond formation using aryl azides as nitrogen source.

Authors+Show Affiliations

Department of Chemistry and Open Laboratory of Chemical Biology of the Institute of Molecular Technology for Drug Discovery and Synthesis, The University of Hong Kong, Pokfulam Road, Hong Kong, China.No affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

20730175

Citation

Liu, Yungen, et al. "[Fe(F(20)TPP)Cl] Catalyzed Intramolecular C-N Bond Formation for Alkaloid Synthesis Using Aryl Azides as Nitrogen Source." Chemical Communications (Cambridge, England), vol. 46, no. 37, 2010, pp. 6926-8.
Liu Y, Wei J, Che CM. [Fe(F(20)TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source. Chem Commun (Camb). 2010;46(37):6926-8.
Liu, Y., Wei, J., & Che, C. M. (2010). [Fe(F(20)TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source. Chemical Communications (Cambridge, England), 46(37), 6926-8. https://doi.org/10.1039/c0cc01825b
Liu Y, Wei J, Che CM. [Fe(F(20)TPP)Cl] Catalyzed Intramolecular C-N Bond Formation for Alkaloid Synthesis Using Aryl Azides as Nitrogen Source. Chem Commun (Camb). 2010 Oct 7;46(37):6926-8. PubMed PMID: 20730175.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Fe(F(20)TPP)Cl] catalyzed intramolecular C-N bond formation for alkaloid synthesis using aryl azides as nitrogen source. AU - Liu,Yungen, AU - Wei,Jinhu, AU - Che,Chi-Ming, Y1 - 2010/08/23/ PY - 2010/8/24/entrez PY - 2010/8/24/pubmed PY - 2010/12/22/medline SP - 6926 EP - 8 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) VL - 46 IS - 37 N2 - The syntheses of alkaloids including indoles, indolines, tetrahydroquinolines, dihydroquinazolinones and quinazolinones have been accomplished in moderate to excellent yields via [Fe(F(20)TPP)Cl] catalyzed intramolecular C-N bond formation using aryl azides as nitrogen source. SN - 1364-548X UR - https://www.unboundmedicine.com/medline/citation/20730175/[Fe_F_20_TPP_Cl]_catalyzed_intramolecular_C_N_bond_formation_for_alkaloid_synthesis_using_aryl_azides_as_nitrogen_source_ L2 - https://doi.org/10.1039/c0cc01825b DB - PRIME DP - Unbound Medicine ER -