Publication:
Iodine-catalyzed oxidative amination of sodium sulfinates: A convenient approach to the synthesis of sulfonamides under mild conditions

Issued Date

2015-01-01

Resource Type

Article

ISSN

10990690
1434193X

DOI

10.1002/ejoc.201403531

Other identifier(s)

2-s2.0-85027934131

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

European Journal of Organic Chemistry. Vol.2015, No.7 (2015), 1575-1582

Suggested Citation

Chonchanok Buathongjan, Danupat Beukeaw, Sirilata Yotphan Iodine-catalyzed oxidative amination of sodium sulfinates: A convenient approach to the synthesis of sulfonamides under mild conditions. European Journal of Organic Chemistry. Vol.2015, No.7 (2015), 1575-1582. doi:10.1002/ejoc.201403531 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/35766

Research Projects

Organizational Units

Authors

Journal Issue

Thesis

Title

Iodine-catalyzed oxidative amination of sodium sulfinates: A convenient approach to the synthesis of sulfonamides under mild conditions

Author(s)

Chonchanok Buathongjan
 Danupat Beukeaw
 Sirilata Yotphan

Other Contributor(s)

Mahidol University

Abstract

© 2015 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. The iodine-catalyzed oxidative amination of sodium sulfinates in the presence of sodium percarbonate as the oxidant has been developed. The reaction shows good substrate scope and tolerates a wide range of functionalities in both amine and sodium sulfinate substrates. Aliphatic amines, heteroaromatic amines and hydrochloride salts of amines canbe employed as the amine sources in this transformation. Mechanistic studies indicated that a radical pathway might be involved in the reaction process. This transition-metalfree protocol offers an alternative and convenient approach for a preparation of a series of sulfonamides in moderate to good yields under mild conditions.

Keyword(s)

Chemistry

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/35766

Collections

Scopus 2011-2015