Journal article

General synthesis of sugar-derived azepane nitrones: precursors of azepane iminosugars.

Abstract:: A general and efficient method has been developed for the synthesis of sugar-derived azepane nitrones starting from aldohexoses, with an intramolecular condensation of aldehyde and hydroxylamine as the key step. Through this strategy, each aldohexose produced a pair of azepane nitrones, which are precursors of various azepane iminosugars.

Publication status:: Published

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APA Style

Zhao, W., Nakagawa, S., Kato, A., Adachi, I., Jia, Y., Hu, X., Fleet, G., Wilson, F., Horne, G., Yoshihara, A., Izumori, K., & Yu, C. (2013). General synthesis of sugar-derived azepane nitrones: precursors of azepane iminosugars. Journal of Organic Chemistry, 78(7), 3208–3221.

MLA Style

Zhao, W, et al. “General Synthesis of Sugar-Derived Azepane Nitrones: Precursors of Azepane Iminosugars.” Journal of Organic Chemistry, vol. 78, no. 7, 2013, pp. 3208–21.

Chicago Style

Zhao, W, S Nakagawa, A Kato, et al. 2013. “General Synthesis of Sugar-Derived Azepane Nitrones: Precursors of Azepane Iminosugars.” Journal of Organic Chemistry 78 (7): 3208–21.
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Publisher copy:: 10.1021/jo400130p

Authors

+ Zhao, W More by this author

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+ Nakagawa, S More by this author

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+ Kato, A More by this author

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+ Adachi, I More by this author

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+ Jia, Y More by this author

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Journal:: Journal of organic chemistry More from this journal
Volume:: 78
Issue:: 7
Pages:: 3208-3221
Publication date:: 2013-04-01
DOI:: 10.1021/jo400130p
EISSN:: 1520-6904
ISSN:: 0022-3263

Language:: English
Keywords:: Nitrogen Oxides

Carbohydrates

Molecular Structure
Pubs id:: pubs:405083
UUID:: uuid:f1ee9f5d-deb2-44d1-beed-152adb0f7e9b
Local pid:: pubs:405083
Source identifiers:: 405083
Deposit date:: 2013-11-17
ARK identifier:: ark:/29072/ora_f1ee9f5ddeb244d1beed152adb0f7e9b

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Copyright date:: 2013

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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