Pd-catalyzed arylation of chlorotrifluoroethylene using arylboronic acids.Org Lett. 2012 Jul 06; 14(13):3454-7.OL
Abstract
The palladium-catalyzed cross-coupling of chlorotrifluoroethylene and arylboronic acids proceeds in the presence of a base and H(2)O to provide α,β,β-trifluorostyrene derivatives in satisfactory yields.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
22691065
Citation
Yamamoto, Tetsuya, and Tetsu Yamakawa. "Pd-catalyzed Arylation of Chlorotrifluoroethylene Using Arylboronic Acids." Organic Letters, vol. 14, no. 13, 2012, pp. 3454-7.
Yamamoto T, Yamakawa T. Pd-catalyzed arylation of chlorotrifluoroethylene using arylboronic acids. Org Lett. 2012;14(13):3454-7.
Yamamoto, T., & Yamakawa, T. (2012). Pd-catalyzed arylation of chlorotrifluoroethylene using arylboronic acids. Organic Letters, 14(13), 3454-7. https://doi.org/10.1021/ol3014107
Yamamoto T, Yamakawa T. Pd-catalyzed Arylation of Chlorotrifluoroethylene Using Arylboronic Acids. Org Lett. 2012 Jul 6;14(13):3454-7. PubMed PMID: 22691065.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Pd-catalyzed arylation of chlorotrifluoroethylene using arylboronic acids.
AU - Yamamoto,Tetsuya,
AU - Yamakawa,Tetsu,
Y1 - 2012/06/12/
PY - 2012/6/14/entrez
PY - 2012/6/14/pubmed
PY - 2012/11/8/medline
SP - 3454
EP - 7
JF - Organic letters
JO - Org Lett
VL - 14
IS - 13
N2 - The palladium-catalyzed cross-coupling of chlorotrifluoroethylene and arylboronic acids proceeds in the presence of a base and H(2)O to provide α,β,β-trifluorostyrene derivatives in satisfactory yields.
SN - 1523-7052
UR - https://www.unboundmedicine.com/medline/citation/22691065/Pd_catalyzed_arylation_of_chlorotrifluoroethylene_using_arylboronic_acids_
L2 - https://doi.org/10.1021/ol3014107
DB - PRIME
DP - Unbound Medicine
ER -
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