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

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Bibliographic Details
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]
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Database: Engineering Source
Description
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]
ISSN:00223263
DOI:10.1021/jo034679b