Organic compounds of fluorine. XI. The synthesis of δ, δ-difluoronorleucine
M Hudlický
Index: Collection of Czechoslovak Chemical Communications, , vol. 32, p. 453 - 457
Full Text: HTML
Citation Number: 6
Abstract
... In our last communication 1 we described the synthesis of o-fluoronorleucine. ... was continued for 3 hours at room temperature and for 2 hours at 30°C. Hydrogen fluoride was allowed to evaporate, the oily residue was diluted with an equal volume of ether ... Collection Czechoslov. ...
Related Articles:
[Paine, John B.; Brough, Jonathan R.; Buller, Kathy K.; Erikson, Erika E. Journal of Organic Chemistry, 1987 , vol. 52, # 18 p. 3986 - 3993]
[Brun, Paola; Dean, Annalisa; Di Marco, Valerio; Surajit, Pathak; Castagliuolo, Ignazio; Carta, Davide; Ferlin, Maria Grazia European Journal of Medicinal Chemistry, 2013 , vol. 62, p. 486 - 497]
The synthesis and application of novel nitrating and nitrosating agents
[Hakimelahi, Gholam H.; Sharghi, Hashem; Zarrinmayeh, Hamide; Khalafi-Nezhad, Ali Helvetica Chimica Acta, 1984 , vol. 67, p. 906 - 915]
Amination of ester enolates with O-(2, 4-dinitrophenyl) hydroxylamine
[Journal of Organic Chemistry, , vol. 44, p. 4836 - 4841]