Mechanistic and computational studies of oxidatively-induced Aryl-CF 3 bond-formation at Pd: Rational design of room temperature aryl trifluoromethylation

Nicholas D. Ball; J. Brannon Gary; Yingda Ye; Melanie S. Sanford

doi:10.1021/ja201726q

Mechanistic and computational studies of oxidatively-induced Aryl-CF ₃ bond-formation at Pd: Rational design of room temperature aryl trifluoromethylation

Nicholas D. Ball
, J. Brannon Gary
, Yingda Ye
, Melanie S. Sanford

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	7577-7584
Number of pages	8
Journal	Journal of the American Chemical Society
Volume	133
Issue number	19
DOIs	https://doi.org/10.1021/ja201726q
State	Published - May 18 2011
Externally published	Yes

ASJC Scopus Subject Areas

Catalysis
Biochemistry
General Chemistry
Colloid and Surface Chemistry

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10.1021/ja201726q

Cite this

Mechanistic and computational studies of oxidatively-induced Aryl-CF ₃ bond-formation at Pd: Rational design of room temperature aryl trifluoromethylation. / Ball, Nicholas D.; Gary, J. Brannon; Ye, Yingda et al.
In: Journal of the American Chemical Society, Vol. 133, No. 19, 18.05.2011, p. 7577-7584.

Research output: Contribution to journal › Article › peer-review

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T2 - Rational design of room temperature aryl trifluoromethylation

AU - Ball, Nicholas D.

AU - Gary, J. Brannon

AU - Ye, Yingda

AU - Sanford, Melanie S.

PY - 2011/5/18

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JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

IS - 19

ER -

Mechanistic and computational studies of oxidatively-induced Aryl-CF 3 bond-formation at Pd: Rational design of room temperature aryl trifluoromethylation

ASJC Scopus Subject Areas

Access to Document

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Cite this

Mechanistic and computational studies of oxidatively-induced Aryl-CF ₃ bond-formation at Pd: Rational design of room temperature aryl trifluoromethylation