Lewis acid-promoted 3-aza-Cope rearrangement of N-alkyl-N-allylanilines
LG Beholz, JR Stille
Index: Journal of Organic Chemistry, , vol. 58, # 19 p. 5095 - 5100
Full Text: HTML
Citation Number: 39
Abstract
... Department of Chemistry, Michigan State University, East Lansing, Michigan 48824 ... of products resulting from removal of the allyl group, have restricted the utility of this reaction and presented an enormous challenge to synthetic organic chemists.2 Approaches to ... 5096 J. Org. ...
Related Articles:
Synthesis of indoles via alkylidenation of acyl hydrazides
[Hisler, Kevin; Commeureuc, Aurelien G.J.; Zhou, Sheng-ze; Murphy, John A. Tetrahedron Letters, 2009 , vol. 50, # 26 p. 3290 - 3293]
FeCl3· 6H2O-Catalyzed Alkenylation of Indoles with Aldehydes
[Journal of Organic Chemistry, , vol. 77, # 18 p. 8355 - 8361]
[Journal of Medicinal Chemistry, , vol. 39, # 4 p. 892 - 903]
[Journal of Medicinal Chemistry, , vol. 39, # 4 p. 892 - 903]
[Russian Chemical Bulletin, , vol. 59, # 12 p. 2236 - 2246]