111980-33-7Relevant articles and documents
Synthesis of morpholin-2-ones by chemoselective intramolecular rhodium-catalyzed reductive ring expansion of oxazolidines
Vasylyev, Maksym,Alper, Howard
supporting information; experimental part, p. 1357 - 1359 (2009/05/07)
(Chemical Equation Presented) The rhodium-catalyzed reductive intramolecular ring expansion of N-(ethoxycarboxymethyl)oxazolidines was carried out under an atmosphere of carbon monoxide and hydrogen to afford N-methylmorpholin-2-ones in good to excellent
ASYMMETRIC SYNTHESIS X : A CHIRAL PYRROLIDINE SYNTHON FOR A NEW APPROACH TO THE SYNTHESIS OF ALKALOIDS
Huang, P. Q.,Arseniyadis, S.,Husson, H. -P.
, p. 547 - 550 (2007/10/02)
The synthesis of chiral 2-cyano-5-oxazolopyrrolidine 3 is reported.The synthesis of the optically pure ant venom alkaloid, (+)-(S)-trans-2-heptyl-5-butyl-pyrrolidine 7, has been achieved from 3.
