Photoredox-catalyzed sulfenylation/cyclization of N-aryl-N-tosylpropargylamine with disulfide: A concise route to 3-phenylthioquinoline. Issue 20 (17th May 2019)
- Record Type:
- Journal Article
- Title:
- Photoredox-catalyzed sulfenylation/cyclization of N-aryl-N-tosylpropargylamine with disulfide: A concise route to 3-phenylthioquinoline. Issue 20 (17th May 2019)
- Main Title:
- Photoredox-catalyzed sulfenylation/cyclization of N-aryl-N-tosylpropargylamine with disulfide: A concise route to 3-phenylthioquinoline
- Authors:
- Wang, Yu-Zhao
Zhang, Heng-Rui
Zhou, Li
Fang, Jun-Dan
Liu, Xue-Yuan - Abstract:
- Abstract: A facile and novel protocol for one-pot synthesis of 3-phenylthioquinoline derivates via visible-light induced tandem cyclization of N -aryl- N -tosylpropargylamine with disulfides was developed. This unprecedented method, involving CS bond formation, detosylation and aromatization, afforded the desired products in a broad substrate scope under mild conditions. Graphical abstract: Image 1
- Is Part Of:
- Tetrahedron. Volume 75:Issue 20(2019)
- Journal:
- Tetrahedron
- Issue:
- Volume 75:Issue 20(2019)
- Issue Display:
- Volume 75, Issue 20 (2019)
- Year:
- 2019
- Volume:
- 75
- Issue:
- 20
- Issue Sort Value:
- 2019-0075-0020-0000
- Page Start:
- 2893
- Page End:
- 2899
- Publication Date:
- 2019-05-17
- Subjects:
- Photoredox catalysis -- Tandem cyclization -- CS bond formation -- Detosylation -- Aromatization
Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.tet.2019.04.017 ↗
- Languages:
- English
- ISSNs:
- 0040-4020
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8796.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10134.xml