Publication:
Convenient synthesis of α-nitrooximes mediated by OXONE®

Issued Date

2014-01-01

Resource Type

Article

ISSN

20462069

DOI

10.1039/c4ra11703d

Other identifier(s)

2-s2.0-84912038846

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

RSC Advances. Vol.4, No.104 (2014), 59726-59732

Suggested Citation

Napasawan Chumnanvej, Natthapol Samakkanad, Manat Pohmakotr, Vichai Reutrakul, Thaworn Jaipetch, Darunee Soorukram, Chutima Kuhakarn Convenient synthesis of α-nitrooximes mediated by OXONE®. RSC Advances. Vol.4, No.104 (2014), 59726-59732. doi:10.1039/c4ra11703d Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/33576

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Title

Convenient synthesis of α-nitrooximes mediated by OXONE®

Author(s)

Napasawan Chumnanvej
 Natthapol Samakkanad
 Manat Pohmakotr
 Vichai Reutrakul
 Thaworn Jaipetch
 Darunee Soorukram
 Chutima Kuhakarn

Other Contributor(s)

Mahidol University

Abstract

© The Royal Society of Chemistry 2014. A novel OXONE® mediated direct difunctionalization of alkenes with NaNO<inf>2</inf> in aqueous acetonitrile for the synthesis of α-nitrooximes was developed. The α-nitrooximes were readily prepared in moderate to high yields at room temperature under mild reaction conditions. The present protocol offers an easy and environmentally benign approach to access various α-nitrooximes derived from styrene derivatives.

Keyword(s)

Chemical Engineering
 Chemistry

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/33576

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Scopus 2011-2015