High yield direct fluorofunctionalisation of ketones using accufluor™ - NFTh fluorinating reagent

Tetrahedron Letters

Volumn 37, Issue 20, 1996, Pages 3591-3594

  Stavber, Stojan ^a   Zupan, Marko ^a  

^a UNIVERSITY OF LJUBLJANA   (Slovenia)

Author keywords

[No Author keywords available]

Indexed keywords

KETONE; ORGANOFLUORINE DERIVATIVE;

ARTICLE; FLUORINATION; TECHNIQUE;

EID: 0029996006     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00630-2     Document Type: Article

References (25)

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18. ™ F-TEDA reagents is given in 3c, 3d and: a) Zupan, M.; Stavber, S. Trends in Organic Chemistry. Vol. V, PP. 11-36; Council of Scientific Information: Trivandrum (India), 1995;
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23. ™ NFTh reagent in our research and providing us with free samples of the material.
24. 2.
25. The activity of 1 was determined by iodometric titration which revealed that 1 g of 1 (3.11 mmol; dried for 3 h at 25 °C under reduced pressure) liberated 3.08 ± 0.02 mmol of iodine.