Mechanism of the Reaction of Olefins with Nitrous Anhydride (O═N–O–N═O) to Form 1,2-Oxazetes
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States
Funder
Pfizer
Bristol-Myers Squibb
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c04080
Reference11 articles.
1. Nitrosyl Triflate and Nitrous Anhydride, Same Mode of Generation, but Very Different Reaction Pathways. Direct Synthesis of 1,2-Oxazetes, Nitroso or Bisoxazo Compounds from Olefins
2. A new route to the 4-1,2-oxazete ring system by the stereospecific oxidation of ()-3,3-dimethyl-1,1-(methylthio)-2-butanone oxime
3. 1,3‐Dipolar Cycloaddition Reactions of Nitrile Oxides under “Non‐Conventional” Conditions: Green Solvents, Irradiation, and Continuous Flow
4. 4H-1,2-OxazeteN-Oxides from 1,1-Di-tert-butylallenes
5. Synthesis of Hydroxycedranone and Aminohydroxycedrane
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