4817-80-5Relevant articles and documents
The: Ortho -substituent on 2,4-bis(trifluoromethyl)phenylboronic acid catalyzed dehydrative condensation between carboxylic acids and amines
Wang, Ke,Lu, Yanhui,Ishihara, Kazuaki
supporting information, p. 5410 - 5413 (2018/05/30)
2,4-Bis(trifluoromethyl)phenylboronic acid is a highly effective catalyst for dehydrative amidation between carboxylic acids and amines. Mechanistic studies suggest that a 2:2 mixed anhydride is expected to be the only active species, and the ortho-substituent of boronic acid plays a key role in preventing the coordination of amines to the boron atom of the active species, thus accelerating the amidation. This catalyst works for α-dipeptide synthesis.
DIASTEREOSELECTIVE HYDROGENATION OF METHYL ESTERS OF TRIFLUOROACETYLDEHYDROPHENYLALANYL DIPEPTIDES AND TRIFLUOROACETYLDEHYDROVALYL DIPEPTIDES
Bitiev, Sh. G.,Chel'tsova-Bebutova, G. V.,Karpeiskaya, E. I.,Klabunovskii, E. I.
, p. 1472 - 1475 (2007/10/02)
-