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Unexpected Insertion of Nitrogen into a C-C Bond: Access to 2,3-Disubstituted Quinazolinone Scaffolds
- Source :
- Organic letters. 23(12)
- Publication Year :
- 2021
-
Abstract
- A novel, practical, highly efficient, and transition metal free nitrogen insertion reaction for the synthesis of 2,3-disubstituted quinazolinone derivatives was developed. Diverse functionalized 3-indolinone-2-carboxylates and nitrosoarenes with a wide range of substituted nitrosobenzenes, nitrosopyridines, dibenzofuranyl, or dibenzothienyl nitroso compounds worked smoothly to give 2,3-disubstituted quinazolinone derivatives in good to excellent yields (69-98%). A gram-scale reaction was achieved, and an afloqualone analogue was synthesized under the mild reaction conditions.
- Subjects :
- Reaction conditions
Nitroso Compounds
010405 organic chemistry
Organic Chemistry
chemistry.chemical_element
010402 general chemistry
01 natural sciences
Biochemistry
Nitrogen
Combinatorial chemistry
0104 chemical sciences
chemistry.chemical_compound
chemistry
Transition metal
Insertion reaction
medicine
Afloqualone
Physical and Theoretical Chemistry
Quinazolinone
medicine.drug
Subjects
Details
- ISSN :
- 15237052
- Volume :
- 23
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Organic letters
- Accession number :
- edsair.doi.dedup.....b0aa182d05dd92afe783a426761fe386