Synthesis of a New Stable Conformationally Constrained 2,7-Anhydrosialic Acid Derivative.

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Title: Synthesis of a New Stable Conformationally Constrained 2,7-Anhydrosialic Acid Derivative.
Authors: Ke-Gang Liu1, Hai-Bin Zhou, Bruno1, Yu-Lin Wu1, Zhu-Jun Yao1 yaoz@mail.sioc.ac.cn
Source: Journal of Organic Chemistry. 11/28/2003, Vol. 68 Issue 24, p9528-9531. 4p. 4 Diagrams.
Subjects: Sialic acids, Grignard reagents, Organic synthesis
Abstract: A stereoseletive synthesis of 2,7-anhydrosialic acid derivative 18 was achieved from D-glucono-δ-1actone. A highly syn-selective addition of Grignard reagent to the N-benzylimine 8 served as a key step. [ABSTRACT FROM AUTHOR]
Copyright of Journal of Organic Chemistry is the property of American Chemical Society and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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An: 11751805
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  Data: Synthesis of a New Stable Conformationally Constrained 2,7-Anhydrosialic Acid Derivative.
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  Data: <searchLink fieldCode="AR" term="%22Ke-Gang+Liu%22">Ke-Gang Liu</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Hai-Bin+Zhou%2C+Bruno%22">Hai-Bin Zhou, Bruno</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Yu-Lin+Wu%22">Yu-Lin Wu</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Zhu-Jun+Yao%22">Zhu-Jun Yao</searchLink><relatesTo>1</relatesTo><i> yaoz@mail.sioc.ac.cn</i>
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Organic+Chemistry%22">Journal of Organic Chemistry</searchLink>. 11/28/2003, Vol. 68 Issue 24, p9528-9531. 4p. 4 Diagrams.
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  Data: <searchLink fieldCode="DE" term="%22Sialic+acids%22">Sialic acids</searchLink><br /><searchLink fieldCode="DE" term="%22Grignard+reagents%22">Grignard reagents</searchLink><br /><searchLink fieldCode="DE" term="%22Organic+synthesis%22">Organic synthesis</searchLink>
– Name: Abstract
  Label: Abstract
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  Data: A stereoseletive synthesis of 2,7-anhydrosialic acid derivative 18 was achieved from D-glucono-δ-1actone. A highly syn-selective addition of Grignard reagent to the N-benzylimine 8 served as a key step. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
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  Data: <i>Copyright of Journal of Organic Chemistry is the property of American Chemical Society and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1021/jo034679b
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        Text: English
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      – SubjectFull: Sialic acids
        Type: general
      – SubjectFull: Grignard reagents
        Type: general
      – SubjectFull: Organic synthesis
        Type: general
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      – TitleFull: Synthesis of a New Stable Conformationally Constrained 2,7-Anhydrosialic Acid Derivative.
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            NameFull: Ke-Gang Liu
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            NameFull: Hai-Bin Zhou, Bruno
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            NameFull: Yu-Lin Wu
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              Text: 11/28/2003
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              Y: 2003
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