195299-15-1Relevant articles and documents
ASYMMETRIC SYNTHESIS XII: STEREOCONTROLLED ELECTROPHILIC-NUCLEOPHILIC α,α'-SUBSTITUTION OF THE PYRROLIDINE RING.
Arseniyadis, S.,Huang, P. Q.,Piveteau, D.,Husson, H.-P.
, p. 2457 - 2470 (2007/10/02)
The synthesis of 2-cyano-5-oxazolopyrrolidine 3, a chiral pyrrolidine synthon, is described.Conditions were established that permitted sequential chemoselective reactions at the C-2 aminonitrile (electrophilic substitution) and at the C-5 aminoether (nucl
ASYMMETRIC SYNTHESIS XI : A SHORT SYNTHESIS OF THE CHIRAL PYRROLIDINE SYNTHON, 2-CYANO-5-OXAZOLOPYRROLIDINE
Royer, Jacques,Husson, Henri-Philippe
, p. 6175 - 6178 (2007/10/02)
The Robinson-Schopf condensation of dimethoxytetrahydrofuran with R(-)phenylglycinol in the presence of KCN followed by reflux in ethanol leads to the formation of 2-cyano-5-oxazolopyrrolidine 1b in 52percent overall yield.