A novel ring cleavage reaction of oxazolines
JI Levin, SM Weinreb
Index: Levin, Jeremy I.; Weinreb, Steven M. Tetrahedron Letters, 1982 , vol. 23, # 23 p. 2347 - 2350
Full Text: HTML
Citation Number: 21
Abstract
Oxazolines are now generally recognized as highly versatile synthons in organic chemistry. These readily available heterocycles are effective as carboxylic acid protecting groups,2 and as activators both for various metalation reactions 193 and for aromatic nucleophilic sub- stitutions. 4 Chiral oxazolines have recently played an important role in synthesis of many types of optically active compounds. 4c,d,5,6 ... An important feature of oxazolines is that they
Related Articles:
A FACILE SYNTHESIS OF ACYL-PROTECTED FORMALDEHYDE CYANOHYDRINS
[Byers, Jeffrey H.; Baran, Robert C.; Craig, Molly E.; Jackman, John T. Organic Preparations and Procedures International, 1991 , vol. 23, # 3 p. 373 - 374]
Benzotriazole-mediated alkoxyalkylation and acyloxyalkylation
[Katritzky, Alan R.; Abdel-Fattah, Ashraf A.A.; Idzik, Krzysztof R.; El-Gendy, Bahaa El-Dien M.; Soloducho, Jadwiga Tetrahedron, 2007 , vol. 63, # 28 p. 6477 - 6484]
Synthesis of. alpha.-alkoxyacrylonitriles using substituted diethyl cyanomethylphosphonates
[Dinizo,S.E. et al. Journal of Organic Chemistry, 1976 , vol. 41, # 17 p. 2846 - 2849]