Publication:
O -Iodoxybenzoic Acid (IBX)-Iodine Mediated One-Pot Deacylative Sulfonylation of 1,3-Dicarbonyl Compounds: A Synthesis of β-Carbonyl Sulfones

Issued Date

2017-03-01

Resource Type

Article

ISSN

1437210X
00397881

DOI

10.1055/s-0036-1588900

Other identifier(s)

2-s2.0-84992702665

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Synthesis (Germany). Vol.49, No.5 (2017), 1109-1121

Suggested Citation

Praewpan Katrun, Teerawat Songsichan, Darunee Soorukram, Manat Pohmakotr, Vichai Reutrakul, Chutima Kuhakarn O -Iodoxybenzoic Acid (IBX)-Iodine Mediated One-Pot Deacylative Sulfonylation of 1,3-Dicarbonyl Compounds: A Synthesis of β-Carbonyl Sulfones. Synthesis (Germany). Vol.49, No.5 (2017), 1109-1121. doi:10.1055/s-0036-1588900 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/42205

Research Projects

Organizational Units

Authors

Journal Issue

Thesis

Title

O -Iodoxybenzoic Acid (IBX)-Iodine Mediated One-Pot Deacylative Sulfonylation of 1,3-Dicarbonyl Compounds: A Synthesis of β-Carbonyl Sulfones

Author(s)

Praewpan Katrun
 Teerawat Songsichan
 Darunee Soorukram
 Manat Pohmakotr
 Vichai Reutrakul
 Chutima Kuhakarn

Other Contributor(s)

Mahidol University

Abstract

© Georg Thieme Verlag Stuttgart · New York-Synthesis 2017. A combination of o-iodoxybenzoic acid (IBX) and a catalytic amount of iodine is found to promote a facile one-pot deacylative sulfonylation reaction of 1,3-dicarbonyl compounds with sodium sulfinates to yield β-carbonyl sulfones. The present method provides the target products bearing a wide variety of functional groups in one step and in good yields.

Keyword(s)

Chemical Engineering
 Chemistry

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/42205

Collections

Scopus 2016-2017