Facile synthesis of trifluoroethyl compounds by the Suzuki cross-coupling reactions of CF3CH2OTs with arylboronic acids.
about
Nickel-Catalyzed Alkyl-Alkyl Cross-Couplings of Fluorinated Secondary Electrophiles: A General Approach to the Synthesis of Compounds having a Perfluoroalkyl Substituent.Stereoconvergent Negishi Arylations of Racemic Secondary Alkyl Electrophiles: Differentiating between a CF3 and an Alkyl GroupMetal-free trifluoromethylation of aromatic and heteroaromatic aldehydes and ketones.Nickel-catalyzed direct C-H trifluoroethylation of heteroarenes with trifluoroethyl iodide.Pd-catalyzed divergent trifluoroethylation and arylation of arylboronic acids by aryl(2,2,2-trifluoroethyl)iodonium triflates.
P2860
Facile synthesis of trifluoroethyl compounds by the Suzuki cross-coupling reactions of CF3CH2OTs with arylboronic acids.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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name
Facile synthesis of trifluoroe ...... CH2OTs with arylboronic acids.
@en
Facile synthesis of trifluoroe ...... CH2OTs with arylboronic acids.
@nl
type
label
Facile synthesis of trifluoroe ...... CH2OTs with arylboronic acids.
@en
Facile synthesis of trifluoroe ...... CH2OTs with arylboronic acids.
@nl
prefLabel
Facile synthesis of trifluoroe ...... CH2OTs with arylboronic acids.
@en
Facile synthesis of trifluoroe ...... CH2OTs with arylboronic acids.
@nl
P2093
P2860
P356
P1476
Facile synthesis of trifluoroe ...... CH2OTs with arylboronic acids.
@en
P2093
P2860
P304
10697-10699
P356
10.1039/C3CC46601A
P407
P50
P577
2013-11-01T00:00:00Z