Synthesis of Highly Functionalized 4‐Aminoquinolines. Issue 11 (16th February 2016)
- Record Type:
- Journal Article
- Title:
- Synthesis of Highly Functionalized 4‐Aminoquinolines. Issue 11 (16th February 2016)
- Main Title:
- Synthesis of Highly Functionalized 4‐Aminoquinolines
- Authors:
- Wezeman, Tim
Zhong, Sabilla
Nieger, Martin
Bräse, Stefan - Abstract:
- Abstract: A diverse set of highly substituted 4‐aminoquinolines was synthesized from ynamides, triflic anhydride, 2‐chloropyridine, and readily accessible amides in a mild one‐step procedure. Abstract : Diverse products : Electrophilically activated amides easily react with sulfonyl ynamides to yield a diverse range of substituted 4‐aminoquinolines. The ynamides can be easily modified by Sonogashira processes or generated from dichloroenamide precursors. Any substituent can thus be introduced at the C3 position of the quinoline. 2‐ClPy=2‐chloropyridine, Tf2 O=triflic anhydride.
- Is Part Of:
- Angewandte Chemie international edition. Volume 55:Issue 11(2016)
- Journal:
- Angewandte Chemie international edition
- Issue:
- Volume 55:Issue 11(2016)
- Issue Display:
- Volume 55, Issue 11 (2016)
- Year:
- 2016
- Volume:
- 55
- Issue:
- 11
- Issue Sort Value:
- 2016-0055-0011-0000
- Page Start:
- 3823
- Page End:
- 3827
- Publication Date:
- 2016-02-16
- Subjects:
- 4-aminoquinolines -- heterocycles -- ynamides
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3773 ↗
http://www.interscience.wiley.com/jpages/1433-7851 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/anie.201511385 ↗
- Languages:
- English
- ISSNs:
- 1433-7851
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2149.xml