Transition Metal-Free Cascade Reactions of Alkynols to Afford Isoquinolin-1(2H)-one and Dihydroisobenzofuran Derivatives
Author:
Affiliation:
1. Shanghai Key Laboratory of Functional Materials Chemistry, Key Lab for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Meilong Road 130, Shanghai, 200237 China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo5006312
Reference91 articles.
1. Stereoselective Glycosylations of a Family of 6-Deoxy-1,2-glycals Generated by Catalytic Alkynol Cycloisomerization
2. Convergent Synthesis of Digitoxin: Stereoselective Synthesis and Glycosylation of the Digoxin Trisaccharide Glycal This research was supported by the U.S. National Institutes of Health (CA-59703). F.E.M. also thanks Novartis Pharmaceuticals for unrestricted additional funding (Grant Program for the Support of Academic Research in Synthetic Organic Chemistry).
3. A Flexible Approach toward trans-Fused Polycyclic Tetrahydropyrans. A Synthesis of Prymnesin and Yessotoxin Units
4. Stereoselective Synthesis of d-Desosamine and Related Glycals via Tungsten-Catalyzed Alkynol Cycloisomerization
5. Brønsted Acid-Promoted Glycosylations of Disaccharide Glycal Substructures of the Saccharomicins
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