Diarylborinic Acid-Catalyzed Regioselective Ring Openings of Epoxy Alcohols with Pyrazoles, Imidazoles, Triazoles, and Other Nitrogen Heterocycles
Author:
Affiliation:
1. Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada
Funder
Canada Foundation for Innovation
Kennarshore
Canada Research Chairs
Natural Sciences and Engineering Research Council of Canada
Government of Ontario
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02412
Reference46 articles.
1. Titanium isopropoxide-mediated nucleophilic openings of 2,3-epoxy alcohols. A mild procedure for regioselective ring-opening
2. Nucleophilic opening of 2,3-epoxy acids and amides mediated by titanium isopropoxide. Highly enhanced C-3 selectivity
3. The synthetic methodology of nonracemic glycidol and related 2,3-epoxy alcohols
4. The Chemistry of Epoxy Alcohols
5. The C-2 selective azide opening reaction of trans-2,3-epoxy alcohols by NaN3 and PhB(OH)2
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