Publication:
Lanthanide triflate catalyzed generation of N-acyliminium ions from α-amido sulfones: the synthesis of (1-alkyl-1-aryl)methyl phenyl sulfones

Issued Date

2007-04-02

Resource Type

Article

ISSN

00404039

DOI

10.1016/j.tetlet.2007.02.035

Other identifier(s)

2-s2.0-33847673216

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Tetrahedron Letters. Vol.48, No.14 (2007), 2467-2470

Suggested Citation

Chutima Kuhakarn, Kassrin Tangdenpaisal, Palangpon Kongsaeree, Samran Prabpai, Patoomratana Tuchinda, Manat Pohmakotr, Vichai Reutrakul Lanthanide triflate catalyzed generation of N-acyliminium ions from α-amido sulfones: the synthesis of (1-alkyl-1-aryl)methyl phenyl sulfones. Tetrahedron Letters. Vol.48, No.14 (2007), 2467-2470. doi:10.1016/j.tetlet.2007.02.035 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/24213

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Title

Lanthanide triflate catalyzed generation of N-acyliminium ions from α-amido sulfones: the synthesis of (1-alkyl-1-aryl)methyl phenyl sulfones

Author(s)

Chutima Kuhakarn
 Kassrin Tangdenpaisal
 Palangpon Kongsaeree
 Samran Prabpai
 Patoomratana Tuchinda
 Manat Pohmakotr
 Vichai Reutrakul

Other Contributor(s)

Mahidol University

Abstract

The reaction of α-amido sulfones with various aromatic and heteroaromatic compounds in the presence of a catalytic amount of lanthanide triflate provides a facile route for the synthesis of (1-alkyl-1-aryl)methyl phenyl sulfones. © 2007 Elsevier Ltd. All rights reserved.

Keyword(s)

Biochemistry, Genetics and Molecular Biology
 Chemistry
 Pharmacology, Toxicology and Pharmaceutics

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/24213

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Scopus 2006-2010