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초록
Reaction of B(4)-acylmethyl o-carborane with 2-azido-1,3-dimethylimidazolinium hexafluorophosphate (ADMP) in the presence of 1,8-diazabicyclo[5.4.0]-undec7-ene (DBU) in acetonitrile at 25 degrees C for 3 h produced a wide range of o-carboranylacyl-substituted diazo compounds in high yields with good functional group tolerance.
키워드
acylmethyl o-carborane; diazotization; o-carborane; o-carboranyl-aryl-substituted diazo compound; 2-azido-1,3-dimethylimidazolinium hexafluorophosphate; B-H ACTIVATION; ORGANIC-SYNTHESIS; TRANSFORMATIONS; CYCLOADDITION; ALKENYLATION; AROMATICITY; BONDS
- 제목
- Synthesis of o-carboranyl-acyl-substituted diazo compounds from B(4)-acylmethyl carboranes and 2-azido1,3-dimethylimidazolinium hexafluorophosphate
- 저자
- Maeng, Chanyoung; Ko, Gi Hoon; Lee, Kyungsup; Noh, Hee Chan; Park, Dae Su; Lee, Phil Ho
- 발행일
- 2023-08
- 유형
- Article
- 권
- 44
- 호
- 8
- 페이지
- 693 ~ 699