Diastereoselective Synthesis of Aryl C ‐Glycosides from Glycosyl Esters via C−O Bond Homolysis-Reference-Cited by-同舟云学术

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Diastereoselective Synthesis of Aryl C ‐Glycosides from Glycosyl Esters via C−O Bond Homolysis

Published:2021-03-10 Issue:17 Volume:133 Page:9519-9524
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Wei Yongliang¹,Ben‐zvi Benjamin¹,Diao Tianning¹^ORCID

Affiliation:

1. Chemistry Department New York University 100 Washington Square East New York NY 10003 USA

Funder

National Institute of General Medical Sciences

Alfred P. Sloan Foundation

Camille and Henry Dreyfus Foundation

National Science Foundation

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202014991

Reference117 articles.

1.

2. Structure, activity, synthesis and biosynthesis of aryl-C-glycosides

3. C-Nucleosides To Be Revisited

4. The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold

5. The evolution of antiviral nucleoside analogues: A review for chemists and non-chemists. Part II: Complex modifications to the nucleoside scaffold

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1. Stereoselective Synthesis of C‐Vinyl Glycosides via Nickel‐Catalyzed Cross‐Electrophile Couplings of 1,2‐Glycosyl Orthoesters and Vinyl Halides;Chinese Journal of Chemistry;2024-08-21

2. Application of Redox-Active Ester Catalysis to the Synthesis of Pyranose Alkyl C-Glycosides;Organic Letters;2023-05-12

3. StereoselectiveC‐Aryl Glycosylation by Catalytic Cross‐Coupling of Heteroaryl Glycosyl Sulfones;Angewandte Chemie International Edition;2023-03-24

4. StereoselectiveC‐Aryl Glycosylation by Catalytic Cross‐Coupling of Heteroaryl Glycosyl Sulfones;Angewandte Chemie;2023-03-24

5. Generation and Use of Glycosyl Radicals under Acidic Conditions: Glycosyl Sulfinates as Precursors;Angewandte Chemie International Edition;2023-03-08

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