One-Pot Synthesis of Less Accessible N-Boc-Propargylic Amines through BF3-Catalyzed Alkynylation and Allylation Using Boronic Esters
Author:
Affiliation:
1. Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan
2. School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China
Funder
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00931
Reference42 articles.
1. Direct addition of alkynes to imines and related CN electrophiles: A convenient access to propargylamines
2. The Enantioselective Addition of Alkyne Nucleophiles to Carbonyl Groups
3. Synthesis of Allylic and Propargylic Primary Amines by Reaction of Organometallic Reagents with α-Amidoalkyl Sulfones
4. Cu(I)Br mediated coupling of alkynes with N-acylimine and N-acyliminium ions in water
5. A Practical Gold-Catalyzed Route to 4-Substituted Oxazolidin-2-ones fromN-Boc Propargylamines
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