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dc.contributor.author
Sandeep, Chandrashekharappa
dc.contributor.author
Venugopala, Katharigatta N.
dc.contributor.author
Gleiser, Raquel M.
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dc.contributor.author
Chetram, Abeen
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Padmashali, Basavaraj
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Kulkarni, Rashmi S.
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Venugopala, Rashmi
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Odhav, Bharti
dc.date.available
2023-01-18T16:04:09Z
dc.date.issued
2016-07-21
dc.identifier.citation
Sandeep, Chandrashekharappa; Venugopala, Katharigatta N.; Gleiser, Raquel M.; Chetram, Abeen; Padmashali, Basavaraj; et al.; Greener synthesis of indolizine analogues using water as a base and solvent: Study for larvicidal activity against Anopheles arabiensis; Wiley Blackwell Publishing, Inc; Chemical Biology & Drug Design; 88; 6; 21-7-2016; 899-904
dc.identifier.issn
1747-0277
dc.identifier.uri
http://hdl.handle.net/11336/184912
dc.description.abstract
Greener synthesis of a series of novel indolizine analogues have been achieved by the cyclization of aromatic cycloimmonium ylides with electron-deficient alkynes in the presence of water as the base and solvent at 80 °C. Yield of the title compounds was good and reactions performed were eco-friendly. The structures of these newly synthesized compounds have been confirmed by spectroscopic techniques such as FTIR, NMR, LC-MS, and elemental analysis. Characterized title compounds were evaluated for larvicidal activity against Anopheles arabiensis by standard WHO larvicidal assay using Temefos as standard at 4 μg/mL. Title compounds 2e, 2f, and 2g emerged as promising larvicidal agents.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Wiley Blackwell Publishing, Inc
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dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
CHARACTERIZATION
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INDOLIZINE ANALOGUES
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LARVICIDAL ACTIVITY
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SYNTHESIS
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Bioquímica y Biología Molecular
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Ciencias Biológicas
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dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
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dc.title
Greener synthesis of indolizine analogues using water as a base and solvent: Study for larvicidal activity against Anopheles arabiensis
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2022-12-01T14:24:22Z
dc.identifier.eissn
1747-0285
dc.journal.volume
88
dc.journal.number
6
dc.journal.pagination
899-904
dc.journal.pais
Reino Unido
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dc.journal.ciudad
Londres
dc.description.fil
Fil: Sandeep, Chandrashekharappa. Institute For Stem Cell Biology And Regenerative Medic; India
dc.description.fil
Fil: Venugopala, Katharigatta N.. Durban University Of Technology; Sudáfrica
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Fil: Gleiser, Raquel M.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto Multidisciplinar de Biología Vegetal (P). Grupo Vinculado Centro de Relevamiento y Evaluación de Recursos Agrícolas y Naturales; Argentina
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Fil: Chetram, Abeen. Durban University Of Technology; Sudáfrica
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Fil: Padmashali, Basavaraj. Rani Channamma University; India
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Fil: Kulkarni, Rashmi S.. Jain University; India
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Fil: Venugopala, Rashmi. University Of Kwazulu-natal; Sudáfrica
dc.description.fil
Fil: Odhav, Bharti. Durban University Of Technology; Sudáfrica
dc.journal.title
Chemical Biology & Drug Design
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dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1111/cbdd.12823
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1111/cbdd.12823
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