168112-44-5Relevant articles and documents
SYNTHESIS OF OXAZOLINE COMPOUNDS
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Page/Page column 15; 19-20, (2010/04/03)
The present invention provides an improved process for preparing an oxazoline compound of the formula: (I) wherein R1 and R2 are independently hydrogen, sulfide, sulfoxide, sulfonyl, optionally substituted lower alkyl, optionally sub
THERMAL CYCLIZATION OF Β-HYDROXYAMIDES TO OXAZOLINES
Somanathan, Ratnasamy,Aguilar, Hugo R.,Rivero, Ignacio A.,Aguirre, Gerardo,Hellberg, Lars H.,Yu, Zheng,Thomas, Jacquelin A.
, p. 348 - 353 (2007/10/03)
Thermal conversion of amides derived from erythro and threo ephedrines yields stereospecific oxazolines.
(DIETHYLAMINO)SULFUR TRIFLUORIDE (DAST) AS A USEFUL REAGENT FOR THE PREPARATION OF 2-OXAZOLINES FROM 1,2-AMIDO ALCOHOLS
Lafargue, Pierre,Guenot, Pierre,Lellouche, Jean-Paul
, p. 947 - 958 (2007/10/02)
Acylic 1,2-amido alcohols (6) react efficiently with a slight excess of (diethylamino)sulfur trifluoride (DAST) to afford the corresponding 2-oxazolines (10) in good yields ranging between 57-95percent.Even at the low temperature of -78 deg C, a rapid ( 1 h) and stereoselective amide cyclization is observed without formation of acylaziridine by-products.The scope of this cyclization is discussed.