exo-Imino to endo-Iminocyclitol Rearrangement. A General Route to Five-Membered Antiviral Azasugars-Reference-Cited by-同舟云学术

exo-Imino to endo-Iminocyclitol Rearrangement. A General Route to Five-Membered Antiviral Azasugars

Published:2006-07-15 Issue:16 Volume:8 Page:3465-3467
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Moriarty Robert M.¹,Mitan Carmen I.¹,Branzǎ-Nichita Norica¹,Phares Kenneth R.¹,Parrish Damon¹

Affiliation:

1. University of Illinois at Chicago, Department of Chemistry, Chicago, Illinois 60607, Institute of Biochemistry of the Romanian Academy, Splaiul Independentei 296, 77700 Bucharest, Romania, United Therapeutics Corporation Research, Triangle Park, North Carolina 27709, and Laboratory for the Structure of Matter, Department of the Navy, Naval Research Laboratory, Washington, D.C. 20375

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol061071r

Reference35 articles.

1. Amino-sugar glycosidase inhibitors: versatile tools for glycobiologists

2. Enzyme-catalyzed organic synthesis: practical routes to aza sugars and their analogs for use as glycoprocessing inhibitors

3. Recent Advances in the Total Synthesis of Piperidine Azasugars

4. Imino Sugars That are Less Toxic but More Potent as Antivirals, In Vitro, Compared with N-n-Nonyl DNJ

5. Structure-Activity Relationship of a New Class of Anti-Hepatitis B Virus Agents

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