Stereocontrolled homologation of 1,2 : 3,4-di-O-isopropylidene-α-D-galacto-hexodialdo-1,5-pyranose to 7-deoxynonodialdose epimers via thiazole-aldehyde synthesis-Reference-Cited by-同舟云学术

Stereocontrolled homologation of 1,2 : 3,4-di-O-isopropylidene-α-D-galacto-hexodialdo-1,5-pyranose to 7-deoxynonodialdose epimers via thiazole-aldehyde synthesis

Published:1994 Issue:9 Volume: Page:1231-1239
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Dondoni Alessandro,Ianelli Sandra,Kniezo Ladislav,Merino Pedro,Nardelli Mario

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1994/P1/P19940001231

Reference46 articles.

1. A. Dondoni , Carbohydrate Synthesis via Thiazoles, in Modern Synthetic Methods, ed. R. Scheffold, Verlag Helvetica Chimica Acta, Basel, 1992, p. 377;

2. Acyclic Diastereoselective Synthesis Using Functionalized Thiazoles. Routes to Carbohydrates and Related Natural Products

3. Chemistry of the enolates of 2-acetylthiazole: aldol reactions with chiral aldehydes to give 3-deoxy aldos-2-uloses and 3-deoxy 2-ulosonic acids. A short total synthesis of 3-deoxy-D-manno-2-octulosonic acid (KDO)

4. Stereoselective construction of polyhydroxyalkyl 2-thiazolyl ketones (thiazole ketoses) from d-glyceraldehyde and d-arabinose acetonides by wittig-michael sequence. a route to d-gluco-KDO

5. Installation of the Pyruvate Unit in Glycidic Aldehydes via a Wittig Olefination-Michael Addition Sequence Utilizing a Thiazole-Armed Carbonyl Ylide. A New Stereoselective Route to 3-Deoxy-2-Ulosonic Acids and the Total Synthesis of DAH, KDN, and 4-epi-KDN

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