Intramolecular Displacement Reactions Involving Sulfur Leading to the Formation of 3,6‐Thiaanhydro Sugar Derivatives during the Synthesis of 3,5‐Dithio‐glucofuranose-Reference-Cited by-同舟云学术

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Intramolecular Displacement Reactions Involving Sulfur Leading to the Formation of 3,6‐Thiaanhydro Sugar Derivatives during the Synthesis of 3,5‐Dithio‐glucofuranose

Published:2022-03 Issue:9 Volume:2022 Page:
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur J Org Chem

Author:

Liao Xiaoxiao¹²^ORCID,Yuan Kai¹,Crich David²³⁴⁵^ORCID

Affiliation:

1. Hunan Key Laboratory of Molecular Precision Medicine Department of Oncology Xiangya Hospital Central South University Changsha Hunan China

2. Department of Chemistry Wayne State University Detroit Michigan 48202 United States

3. Department of Pharmaceutical and Biomedical Sciences University of Georgia Athens Georgia 30602 United States

4. Department of Chemistry University of Georgia Athens Georgia 30602 United States

5. Complex Carbohydrate Research Center University of Georgia Athens Georgia 30602 United States

Funder

National Institutes of Health

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202101496

Reference25 articles.

1. For reviews see:

2. Sugar derivatives having sulfur in the ring

3. Strategies for introducing sulfur atom in a sugar ring: synthesis of 5-thioaldopyranoses and their NMR data

4. 5-Thio-D-Glucose Selectively Potentiates Hyperthermic Killing of Hypoxic Tumor Cells

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