Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols

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 addit...

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Main Authors: Chen, Ke, Li, Yongxin, Pullarkat, Sumod A., Leung, Pak-Hing
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/98294
http://hdl.handle.net/10220/12331
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-982942020-03-07T12:34:46Z Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols Chen, Ke Li, Yongxin Pullarkat, Sumod A. Leung, Pak-Hing School of Physical and Mathematical Sciences 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. 2013-07-26T01:43:01Z 2019-12-06T19:53:17Z 2013-07-26T01:43:01Z 2019-12-06T19:53:17Z 2012 2012 Journal Article 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. 1615-4150 https://hdl.handle.net/10356/98294 http://hdl.handle.net/10220/12331 10.1002/adsc.201100424 en Advanced synthesis & catalysis © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description 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.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Chen, Ke
Li, Yongxin
Pullarkat, Sumod A.
Leung, Pak-Hing
format Article
author Chen, Ke
Li, Yongxin
Pullarkat, Sumod A.
Leung, Pak-Hing
spellingShingle Chen, Ke
Li, Yongxin
Pullarkat, Sumod A.
Leung, Pak-Hing
Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols
author_sort Chen, Ke
title Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols
title_short Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols
title_full Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols
title_fullStr Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols
title_full_unstemmed Palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols
title_sort palladacycle-catalyzed tandem allylic amination/allylation protocol for one-pot synthesis of 2-allylanilines from allylic alcohols
publishDate 2013
url https://hdl.handle.net/10356/98294
http://hdl.handle.net/10220/12331
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