Base-mediated ketenimine formation from N-sulfonylthioimidates for the synthesis of 5-amino-1-vinyl/aryl-1, 2, 3-triazoles. Issue 10 (12th January 2023)
- Record Type:
- Journal Article
- Title:
- Base-mediated ketenimine formation from N-sulfonylthioimidates for the synthesis of 5-amino-1-vinyl/aryl-1, 2, 3-triazoles. Issue 10 (12th January 2023)
- Main Title:
- Base-mediated ketenimine formation from N-sulfonylthioimidates for the synthesis of 5-amino-1-vinyl/aryl-1, 2, 3-triazoles
- Authors:
- Chen, Wan-Yu
Lin, Wei-Han
Kuo, Chia-Jou
Liang, Chien-Fu - Abstract:
- Abstract : N -Sulfonylthioimidate was converted to ketenimine under basic conditions. The reaction with vinyl/aryl azides was induced to cause dipolar cycloaddition to form 5-amino-1-vinyl/aryl-1, 2, 3-triazoles. Abstract : N -Sulfonylthioimidate was converted to ketenimine under basic conditions. The reaction with vinyl/aryl azides was induced to cause dipolar cycloaddition to form 5-amino-1-vinyl/aryl-1, 2, 3-triazoles. The advantages of this method are high efficiency, structural diversity of products favorable yields and applicability to gram-scale operations.
- Is Part Of:
- Chemical communications. Volume 59:Issue 10(2023)
- Journal:
- Chemical communications
- Issue:
- Volume 59:Issue 10(2023)
- Issue Display:
- Volume 59, Issue 10 (2023)
- Year:
- 2023
- Volume:
- 59
- Issue:
- 10
- Issue Sort Value:
- 2023-0059-0010-0000
- Page Start:
- 1297
- Page End:
- 1300
- Publication Date:
- 2023-01-12
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cc ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2cc06708k ↗
- Languages:
- English
- ISSNs:
- 1359-7345
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3139.350000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 25719.xml