A New Indoline Rearrangement
نویسندگان
چکیده
منابع مشابه
Development of a new Lewis acid-catalyzed [3,3]-sigmatropic rearrangement: the allenoate-Claisen rearrangement.
A new Lewis acid-catalyzed Claisen rearrangement has been developed that allows the stereoselective construction of beta-amino-alpha,beta,epsilon,zeta-unsaturated-gamma,delta-disubstituted esters from simple allylic amines and allenoate esters. This reaction, which is contingent upon the use of Lewis acid, can be conducted with a range of metal salts (Yb(OTf)3, AlCl3, Sn(OTf)2, Cu(OTf)2, MgBr2....
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ژورنال
عنوان ژورنال: Canadian Journal of Chemistry
سال: 1972
ISSN: 0008-4042,1480-3291
DOI: 10.1139/v72-399