Exploiting the 1, 2, 3‐Triazole Moiety to Generate Carbazole Molecular Architectures through Click Approach. (29th October 2014)
- Record Type:
- Journal Article
- Title:
- Exploiting the 1, 2, 3‐Triazole Moiety to Generate Carbazole Molecular Architectures through Click Approach. (29th October 2014)
- Main Title:
- Exploiting the 1, 2, 3‐Triazole Moiety to Generate Carbazole Molecular Architectures through Click Approach
- Authors:
- Ameen, Mohamed A.
El‐Shaieb, Kamal M.
Mohamed, Asmaa H.
Abdel‐Latif, Fathy F. - Abstract:
- Abstract : Abstract : Reaction of 3, 6‐dichlorocarbazole with propargyl bromide in the presence of a basic medium gave an N ‐propargylated carbazole. The latter compound was converted into molecular architectures containing 1, 2, 3‐triazole moiety through Cu(I)‐catalyzed1, 3‐cycloaddition reaction with different azides. Similarly, 2‐azidomethyl benzothiazole was cliched with N ‐Boc‐protected N ´‐propargyl glutamate to give the biomolecule 2‐triazolylmethyl product.
- Is Part Of:
- Journal of heterocyclic chemistry. Volume 52:Number 6(2015)
- Journal:
- Journal of heterocyclic chemistry
- Issue:
- Volume 52:Number 6(2015)
- Issue Display:
- Volume 52, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 52
- Issue:
- 6
- Issue Sort Value:
- 2015-0052-0006-0000
- Page Start:
- 1718
- Page End:
- 1722
- Publication Date:
- 2014-10-29
- Subjects:
- Heterocyclic compounds -- Periodicals
547.59 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/jhet.1966 ↗
- Languages:
- English
- ISSNs:
- 0022-152X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4998.200000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1404.xml