Synthesis of aryl azides and vinyl azides via proline-promoted CuI-catalyzed coupling reactions.Chem Commun (Camb). 2004 Apr 07CC
Abstract
The coupling reaction of aryl halides or vinyl iodide with sodium azide under catalysis of CuI/L-proline works at relatively low temperature to provide aryl azides or vinyl azides in good to excellent yields.
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
15045114
Citation
Zhu, Wei, and Dawei Ma. "Synthesis of Aryl Azides and Vinyl Azides Via Proline-promoted CuI-catalyzed Coupling Reactions." Chemical Communications (Cambridge, England), 2004, pp. 888-9.
Zhu W, Ma D. Synthesis of aryl azides and vinyl azides via proline-promoted CuI-catalyzed coupling reactions. Chem Commun (Camb). 2004.
Zhu, W., & Ma, D. (2004). Synthesis of aryl azides and vinyl azides via proline-promoted CuI-catalyzed coupling reactions. Chemical Communications (Cambridge, England), (7), 888-9.
Zhu W, Ma D. Synthesis of Aryl Azides and Vinyl Azides Via Proline-promoted CuI-catalyzed Coupling Reactions. Chem Commun (Camb). 2004 Apr 7;(7)888-9. PubMed PMID: 15045114.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Synthesis of aryl azides and vinyl azides via proline-promoted CuI-catalyzed coupling reactions.
AU - Zhu,Wei,
AU - Ma,Dawei,
Y1 - 2004/03/05/
PY - 2004/3/27/pubmed
PY - 2005/4/20/medline
PY - 2004/3/27/entrez
SP - 888
EP - 9
JF - Chemical communications (Cambridge, England)
JO - Chem Commun (Camb)
IS - 7
N2 - The coupling reaction of aryl halides or vinyl iodide with sodium azide under catalysis of CuI/L-proline works at relatively low temperature to provide aryl azides or vinyl azides in good to excellent yields.
SN - 1359-7345
UR - https://www.unboundmedicine.com/medline/citation/15045114/Synthesis_of_aryl_azides_and_vinyl_azides_via_proline_promoted_CuI_catalyzed_coupling_reactions_
DB - PRIME
DP - Unbound Medicine
ER -
