Efficient synthesis of N-allylated 2-nitroiminoimidazolidine analogues from Baylis–Hillman bromides. Issue 2 (17th January 2017)
- Record Type:
- Journal Article
- Title:
- Efficient synthesis of N-allylated 2-nitroiminoimidazolidine analogues from Baylis–Hillman bromides. Issue 2 (17th January 2017)
- Main Title:
- Efficient synthesis of N-allylated 2-nitroiminoimidazolidine analogues from Baylis–Hillman bromides
- Authors:
- Kumar, Sriramoju Bharath
Pavan Kumar, Chebolu Naga Sesha Sai
Santhoshi, Amlipur
Kumar, Koochana Pranay
Murthy, U. S. N.
Jayathirtha Rao, Vaidya - Abstract:
- ABSTRACT: Various Baylis–Hillman–derived new N -allylated 2-nitroiminoimidazolidine analogs were efficiently prepared using potassium carbonate as base. Simple workup procedure, excellent yields, and mild reaction conditions are the salient features of this method. All the synthesized compounds are screened for their larvicidal activity on fourth instar mosquito larvae, Culex quinquefasciatus . GRAPHICAL ABSTRACT:
- Is Part Of:
- Synthetic communications. Volume 47:Issue 2(2017)
- Journal:
- Synthetic communications
- Issue:
- Volume 47:Issue 2(2017)
- Issue Display:
- Volume 47, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 47
- Issue:
- 2
- Issue Sort Value:
- 2017-0047-0002-0000
- Page Start:
- 131
- Page End:
- 136
- Publication Date:
- 2017-01-17
- Subjects:
- Baylis–Hillman bromides -- insecticidal activity -- N-cinnamyl nitro imino imidazole derivatives -- 2-nitroiminoimidazolidines
Organic compounds -- Synthesis -- Periodicals
Chemistry, Organic
Synthesis
547.205 - Journal URLs:
- http://www.tandfonline.com/toc/lsyc20/current ↗
http://www.tandfonline.com/ ↗ - DOI:
- 10.1080/00397911.2016.1255333 ↗
- Languages:
- English
- ISSNs:
- 0039-7911
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8586.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 644.xml