On the mechanism of the domino reaction of 2-methyl-2-benzyloxycarbonyl-1-indanone mediated by palladium, hydrogen and aminoalcohols
Main Authors: | Caroline Muller, Françoise Hénin, Jacques Muzart |
---|---|
Format: | Article |
Language: | English |
Published: |
Arkat USA, Inc.
2014-11-01
|
Series: | ARKIVOC |
Online Access: | https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p008.805 |
Similar Items
-
(S)-(Z)-Methyl 2-[2,3-bis(benzyloxycarbonyl)guanidino]-4-methylpentanoate
by: Frank R. Fronczek, et al.
Published: (2011-01-01) -
New Methods for the Synthesis of Vicinal Stereocenters : Palladium-Catalyzed Domino Reactions and Asymmetric Transfer Hydrogenation
by: Seashore-Ludlow, Brinton
Published: (2012) -
Studies on Asymmetric Reactions Catalyzed by Chiral 1,2-aminoalcohol
by: Yu-Kai Gao, et al.
Published: (2010) -
Methyl 1-[(Z)-2-(benzyloxycarbonyl)hydrazin-1-ylidene]-5-chloro-2-hydroxyindane-2-carboxylate
by: Kun Dong, et al.
Published: (2014-05-01) -
New Methods for the Synthesis of 3-Substituted 1-Indanones : A Palladium-Catalyzed Approach
by: Arefalk, Anna
Published: (2005)