A Facile and Diastereoselective access to Functionalised Benzopyrano[3, 4-a] Quinolizines via a Pyridine-Based Three-Component Reaction. (December 2017)
- Record Type:
- Journal Article
- Title:
- A Facile and Diastereoselective access to Functionalised Benzopyrano[3, 4-a] Quinolizines via a Pyridine-Based Three-Component Reaction. (December 2017)
- Main Title:
- A Facile and Diastereoselective access to Functionalised Benzopyrano[3, 4-a] Quinolizines via a Pyridine-Based Three-Component Reaction
- Authors:
- Esmaeili, Abbas Ali
Moradi, Abbas
Zangouei, Mahdieh
Fakhari, Ali Reza
Tabibi, Tooba - Abstract:
- The reaction of 2-oxo-2 H -chromene-3-carbonitriles with dialkyl acetylenedicarboxylates and pyridines results in a three-component condensation reaction in which the 2-oxo-2 H -chromene-3-carbonitrile group acts as a dipolarophile to produce benzopyrano[3, 4- a ] quinolizines under mild conditions in good yield.
- Is Part Of:
- Journal of chemical research. Volume 41:Number 12(2017)
- Journal:
- Journal of chemical research
- Issue:
- Volume 41:Number 12(2017)
- Issue Display:
- Volume 41, Issue 12 (2017)
- Year:
- 2017
- Volume:
- 41
- Issue:
- 12
- Issue Sort Value:
- 2017-0041-0012-0000
- Page Start:
- 688
- Page End:
- 692
- Publication Date:
- 2017-12
- Subjects:
- benzopyrano[3, 4-a]quinolizine -- dialkyl acetylenedicarboxylates -- pyridine -- quinolizine
Chemistry -- Research -- Periodicals
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://stl.publisher.ingentaconnect.com/content/stl/jcr ↗
https://journals.sagepub.com/home/chl ↗
http://www.sciencereviews2000.co.uk/ ↗ - DOI:
- 10.3184/174751917X15105690662872 ↗
- Languages:
- English
- ISSNs:
- 1747-5198
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9692.xml