Ugi/Himbert Arene/Allene Diels–Alder Cycloaddition to Synthesize Strained Polycyclic Skeleton
Author:
Affiliation:
1. Department of Chemistry, Innovative Drug Research Center, Shanghai University, Shanghai 200444, P. R. China
2. State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P. R. China
Funder
National Natural Science Foundation of China
State Key Laboratory of Applied Organic Chemistry, Lanzhou University
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b01724
Reference52 articles.
1. Tuning the Reactivity of Isocyano Group: Synthesis of Imidazoles and Imidazoliums from Propargylamines and Isonitriles in the Presence of Multiple Catalysts
2. Triple Role of Phenylselenonyl Group Enabled a One-Pot Synthesis of 1,3-Oxazinan-2-ones From α-Isocyanoacetates, Phenyl Vinyl Selenones, and Water
3. Synthesis of Substituted Pyridines from Cascade [1 + 5] Cycloaddition of Isonitriles to N-Formylmethyl-Substituted Enamides, Aerobic Oxidative Aromatization, and Acyl Transfer Reaction
4. α-Boryl Isocyanides Enable Facile Preparation of Bioactive Boropeptides
5. Recent advances in isocyanide insertion chemistry
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