Indium-mediated mild and efficient one-pot synthesis of alkyl phenyl selenides

Wanida Munbunjong; Eun Hwa Lee; Warinthorn Chavasiri; Doo Ok Jang

doi:10.1016/j.tetlet.2005.10.025

Indium-mediated mild and efficient one-pot synthesis of alkyl phenyl selenides

Wanida Munbunjong, Eun Hwa Lee, Warinthorn Chavasiri, Doo Ok Jang

Chemistry and Medical Chemistry

Research output: Contribution to journal › Article › peer-review

30 Citations (Scopus)

Abstract

A mild and convenient one-pot process for synthesizing alkyl phenyl selenides is developed using indium metal. The reaction shows the selectivity for tert-alkyl, benzylic, and allylic halides over primary and secondary alkyl halides.

Original language	English
Pages (from-to)	8769-8771
Number of pages	3
Journal	Tetrahedron Letters
Volume	46
Issue number	50
DOIs	https://doi.org/10.1016/j.tetlet.2005.10.025
Publication status	Published - 2005 Dec 12

Bibliographical note

Funding Information:
This work was supported by Center for Bioactive Molecular Hybrids at Yonsei University. W.M. is thankful to Thailand Research Fund for the 2004 Royal Golden Jubilee Ph.D. research assistant fellowship.

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2005.10.025

Cite this

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title = "Indium-mediated mild and efficient one-pot synthesis of alkyl phenyl selenides",

abstract = "A mild and convenient one-pot process for synthesizing alkyl phenyl selenides is developed using indium metal. The reaction shows the selectivity for tert-alkyl, benzylic, and allylic halides over primary and secondary alkyl halides.",

author = "Wanida Munbunjong and Lee, {Eun Hwa} and Warinthorn Chavasiri and Jang, {Doo Ok}",

note = "Funding Information: This work was supported by Center for Bioactive Molecular Hybrids at Yonsei University. W.M. is thankful to Thailand Research Fund for the 2004 Royal Golden Jubilee Ph.D. research assistant fellowship.",

year = "2005",

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doi = "10.1016/j.tetlet.2005.10.025",

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journal = "Tetrahedron Letters",

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T1 - Indium-mediated mild and efficient one-pot synthesis of alkyl phenyl selenides

AU - Munbunjong, Wanida

AU - Lee, Eun Hwa

AU - Chavasiri, Warinthorn

AU - Jang, Doo Ok

N1 - Funding Information: This work was supported by Center for Bioactive Molecular Hybrids at Yonsei University. W.M. is thankful to Thailand Research Fund for the 2004 Royal Golden Jubilee Ph.D. research assistant fellowship.

PY - 2005/12/12

Y1 - 2005/12/12

N2 - A mild and convenient one-pot process for synthesizing alkyl phenyl selenides is developed using indium metal. The reaction shows the selectivity for tert-alkyl, benzylic, and allylic halides over primary and secondary alkyl halides.

AB - A mild and convenient one-pot process for synthesizing alkyl phenyl selenides is developed using indium metal. The reaction shows the selectivity for tert-alkyl, benzylic, and allylic halides over primary and secondary alkyl halides.

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DO - 10.1016/j.tetlet.2005.10.025

M3 - Article

AN - SCOPUS:27744442743

VL - 46

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EP - 8771

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 50

ER -

Indium-mediated mild and efficient one-pot synthesis of alkyl phenyl selenides

Abstract

Bibliographical note

All Science Journal Classification (ASJC) codes

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