difluoroacetic acid
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Author(s):  
Zhiwei Chen ◽  
Jie Sun ◽  
Zhiwei Ke ◽  
Xiaoxiao Huang ◽  
Ziwei Li

A facile silver-catalyzed dual decarboxylation of arylthio-difluoroacetic acid with coumarin-3-carboxylic acids/chromone-3-carboxylic acids was developed. This method provided a unique way to synthesize a series of C-4 arylthiodifluoromethylated 3,4-dihydrcoumarins/C-2 arylthiodifluoromethylated chromanones...


mAbs ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1358-1366 ◽  
Author(s):  
Jennifer M. Nguyen ◽  
Jacquelynn Smith ◽  
Susan Rzewuski ◽  
Cristina Legido-Quigley ◽  
Matthew A. Lauber

2019 ◽  
Vol 58 (26) ◽  
pp. 8829-8833 ◽  
Author(s):  
Claudio F. Meyer ◽  
Sandrine M. Hell ◽  
Antonio Misale ◽  
Andrés A. Trabanco ◽  
Véronique Gouverneur
Keyword(s):  

2019 ◽  
Vol 131 (26) ◽  
pp. 8921-8925 ◽  
Author(s):  
Claudio F. Meyer ◽  
Sandrine M. Hell ◽  
Antonio Misale ◽  
Andrés A. Trabanco ◽  
Véronique Gouverneur
Keyword(s):  

Molecules ◽  
2019 ◽  
Vol 24 (6) ◽  
pp. 1039 ◽  
Author(s):  
Ute Dorgerloh ◽  
Roland Becker ◽  
Melanie Kaiser

The concentrations of difluoroacetic acid (DFA) and trifluoroacetic acid (TFA) in rainwater and surface water from Berlin, Germany resembled those reported for similar urban areas, and the TFA/DFA ratio in rainwater of 10:1 was in accordance with the literature. In contrast, nearby ground water historically contaminated with 1,1,2-trichloro-1,2,2-trifluoroethane (R113) displayed a TFA/DFA ratio of 1:3. This observation is discussed versus the inventory of microbial degradation products present in this ground water along with the parent R113 itself. A microbial transformation of chlorotrifluoroethylene (R1113) to DFA so far has not been reported for environmental media, and is suggested based on well-established mammalian metabolic pathways.


Synlett ◽  
2018 ◽  
Vol 29 (14) ◽  
pp. 1847-1850
Author(s):  
Yang Li ◽  
Lan-Ting Shi ◽  
Wen-Qing Zhu ◽  
Hong Li ◽  
Qiang Zhang

By using 2-(fluorosulfonyl)difluoroacetic acid as sulfur ­reagent, bisindole sulfanes were highly efficient synthesized under transition-metal-free conditions. Results indicate that this proceeded not at the relatively acidic C-2 position but rather selectively at the nucleo­philic C-3 position to give the desired compounds with excellent regio­selectivities and good yields.


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