상세 보기
초록
A synthetic route to a wide range of 2-alkoxyaryl-2-aryl enamines is developed from Rh-catalyzed alkoxyarylation of N-sulfonyl-4-aryl-1,2,3-triazoles with aryl ethers via the elimination of nitrogen molecule. In addition, 2-alkoxyaryl-2-aryl enamines are prepared via tandem Cu-catalyzed cycloaddition and Rh-catalyzed alkoxyarylation starting from apes, N-sulfonyl azides, and aryl ethers in one-pot.
키워드
TERMINAL ALKYNES; CONTROLLING SELECTIVITY; AZAVINYL CARBENES; TRANSANNULATION; 1,2,3-TRIAZOLES; PYRROLES; 1-SULFONYL-1,2,3-TRIAZOLES; N-SULFONYL-1,2,3-TRIAZOLES; ANNULATION; TRIAZOLES
- 제목
- Synthesis of 2-Alkoxyaryl-2-aryl Enamines via Tandem Copper-Catalyzed Cycloaddition and Rhodium-Catalyzed Alkoxyarylation from Alkynes, N-Sulfonyl Azides, and Aryl Ethers
- 저자
- Shin, Seohyun; Park, Youngchul; Kim, Cheol-Eui; Son, Jeong-Yu; Lee, Phil Ho
- 발행일
- 2015-06-05
- 유형
- Article
- 권
- 80
- 호
- 11
- 페이지
- 5859 ~ 5869