Literature DB >> 19012432

Application of secondary alkyl halides to a domino aryl alkylation reaction for the synthesis of aromatic heterocycles.

Alena Rudolph1, Nils Rackelmann, Marc-Olivier Turcotte-Savard, Mark Lautens.   

Abstract

A palladium-catalyzed, norbornene-mediated ortho-alkylation reaction of aryl iodides with secondary alkyl halides is described. Intermolecular or intramolecular ortho-alkylation proceeds in a domino process with various termination steps, generating two new carbon-carbon or carbon-nitrogen bonds in one pot, to afford an array of polycyclic heterocycles. The use of enantioenriched substrates has shown that this palladium-catalyzed reaction is stereospecific, proceeding with minimal erosion of ee.

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Year:  2009        PMID: 19012432     DOI: 10.1021/jo802180h

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

Review 1.  Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature.

Authors:  C Oliver Kappe; Doris Dallinger
Journal:  Mol Divers       Date:  2009-04-21       Impact factor: 2.943

2.  Palladium/Norbornene Cooperative Catalysis.

Authors:  Jianchun Wang; Guangbin Dong
Journal:  Chem Rev       Date:  2019-04-25       Impact factor: 60.622

3.  Modular Entry to Functionalized Tetrahydrobenzo[b]azepines via the Palladium/Norbornene Cooperative Catalysis Enabled by a C7-Modified Norbornene.

Authors:  Xin Liu; Jianchun Wang; Guangbin Dong
Journal:  J Am Chem Soc       Date:  2021-06-23       Impact factor: 16.383

  3 in total

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