Lewis Acid Catalyzed Cyclization of Glycals/2-Deoxy-d-ribose with Arylamines: Additional Findings on Product Structure and Reaction Diastereoselectivity-Reference-Cited by-同舟云学术

Lewis Acid Catalyzed Cyclization of Glycals/2-Deoxy-d-ribose with Arylamines: Additional Findings on Product Structure and Reaction Diastereoselectivity

Published:2011-10-07 Issue:21 Volume:76 Page:8833-8839
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Du Chengtang¹²,Li Fulong¹³,Zhang Xuefeng¹,Hu Wenxiang²,Yao Qizheng³,Zhang Ao²

Affiliation:

1. Synthetic Organic & Medicinal Chemistry Laboratory (SOMCL), Shanghai Institute of Materia Medica (SIMM), Shanghai 201203, China

2. Chemistry Department, Capital Normal University, Beijing 100048, China

3. Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing 210009, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo2015483

Reference22 articles.

1. Recent developments in the synthesis of C-glycosides

2. Substitution-with-Allylic-Rearrangement Reactions of Glycal Derivatives

3. Stereoselective C-Glycosidations with Achiral and Enantioenriched Allenylsilanes

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