725277-40-7Relevant academic research and scientific papers
A domino copper-catalyzed C-N and C-O cross-coupling for the conversion of primary amides into oxazoles
Schuh, Kerstin,Glorius, Frank
, p. 2297 - 2306 (2008/02/13)
A variety of oxazoles can efficiently be prepared, in a single step and in good yield, from primary amides and 1,2-dihaloalkenes using copper-catalysis. This new method allows the regioselective formation of a range of substituted oxazoles. The required 1,2-dihaloalkenes can prepared by simple treatment of alkynes with elemental bromine or iodine. Georg Thieme Verlag Stuttgart.
Bromination of Silatranyl-, Germatranyl-, Silyl-, and Germyl-phenylacetylenes
Selina, Anastasia A.,Karlov, Sergey S.,Gauchenova, Ekaterina V.,Churakov, Andrei V.,Kuz'mina, Lyudmila G.,Howard, Judith A.K.,Lorberth, Joerg,Zaitseva, Galina S.
, p. 43 - 56 (2007/10/03)
Reactions of element-substituted alkynes R3MC≡CPh (R 3M = Me3Si, Et3Si, Ph3Si, Et 3Ge, n-Bu3Sn, N(CH2CH2O) 3Si, N(CH2CH2O)
