Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/98294
Title: Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols
Authors: Chen, Ke
Li, Yongxin
Pullarkat, Sumod A.
Leung, Pak-Hing
Issue Date: 2012
Source: Chen, K., Li, Y., Pullarkat, S. A., & Leung, P.-H. (2012). Palladacycle-Catalyzed Tandem Allylic Amination/Allylation Protocol for One-Pot Synthesis of 2-Allylanilines from Allylic Alcohols. Advanced Synthesis & Catalysis, 354(1), 83-87.
Series/Report no.: Advanced synthesis & catalysis
Abstract: An efficient methodology involving the predominant formation of CC bonds is described for the first direct synthesis of 2-allylanilines from allylic alcohols via a one-pot tandem allylic amination/allylation protocol catalyzed by a palladacycle under mild conditions without the requirement for additional activators.
URI: https://hdl.handle.net/10356/98294
http://hdl.handle.net/10220/12331
ISSN: 1615-4150
DOI: 10.1002/adsc.201100424
Schools: School of Physical and Mathematical Sciences 
Rights: © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

SCOPUSTM   
Citations 10

35
Updated on May 2, 2025

Web of ScienceTM
Citations 10

34
Updated on Oct 25, 2023

Page view(s) 20

753
Updated on May 4, 2025

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.