The Staudinger/aza-Wittig/Grignard reaction as key step for the concise synthesis of 1-C-Alkyl-iminoalditol glycomimetics-Reference-Cited by-同舟云学术

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The Staudinger/aza-Wittig/Grignard reaction as key step for the concise synthesis of 1-C-Alkyl-iminoalditol glycomimetics

Published:2016-06 Issue: Volume:429 Page:62-70
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Zoidl Manuel,Gonzalez Santana Andres,Torvisco Ana,Tysoe Christina,Siriwardena Aloysius,Withers Stephen G.,Wrodnigg Tanja M.

Funder

Austrian Academy of Sciences

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference54 articles.

1. Imino sugars and glycosyl hydrolases

2. Iminosugars: from synthesis to therapeutic applications,2007

3. Natural and Synthetic Iminosugars as Carbohydrate Processing Enzyme Inhibitors for Cancer Therapy

4. Organic chemistry of sugars;Greimel,2006

5. Recent Advances in the Total Synthesis of Piperidine Azasugars

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4. Stereoselective Synthesis of 1-C-Diethylphosphonomethyl and -difluoromethyl Iminosugars from Sugar Lactams;The Journal of Organic Chemistry;2022-05-18

5. ANALYSIS OF CARBOHYDRATES AND GLYCOCONJUGATES BY MATRIX‐ASSISTED LASER DESORPTION/IONIZATION MASS SPECTROMETRY: AN UPDATE FOR 2015–2016;Mass Spectrometry Reviews;2021-03-16

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