Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Natalia M. Rougier"'
Autor:
Dyanne L. Cruickshank, Natalia M. Rougier, Raquel V. Vico, Susan A. Bourne, Elba I. Buján, Mino R. Caira, Rita H. de Rossi
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 106-117 (2013)
An anhydrous 1:1 crystalline inclusion complex between the organophosphorus insecticide fenitrothion [O,O-dimethyl O-(3-methyl-4-nitrophenyl)phosphorothioate] and the host compound heptakis(2,6-di-O-methyl)-β-cyclodextrin (DIMEB) was prepared and it
Externí odkaz:
https://doaj.org/article/97dde6c08f2d447c84c236c09c4e61a2
Stabilization of the pesticide Fenitrothion towardOandNnucleophiles in the presence of cyclodextrins
Publikováno v:
Journal of Physical Organic Chemistry. 27:935-943
The reaction of Fenitrothion with O and N nucleophiles (H2O2, NH2OH, n-butylamine and piperidine) was studied at 25 °C in water containing 2% 1,4-dioxane in the presence of native cyclodextrins (α-, β-, and γ-CD). For all the nucleophiles, the pr
Autor:
Mino R. Caira, Dyanne L. Cruickshank, Natalia M. Rougier, Rita H. de Rossi, Susan A. Bourne, Elba I. Buján, Vaughan J. Maurel
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 75:47-56
The X-ray crystal structures of the inclusion complexes formed between three pesticides (two organophosphorus insecticides and one chloroacetanilide herbicide) and permethylated β-cyclodextrin (TRIMEB) are reported. The complexes TRIMEB–fenitrothi
Publikováno v:
The Journal of Organic Chemistry. 75:3427-3436
The reactivity of Fenitrothion (1) toward several O- and N-based nucleophiles, including ambident and alpha-nucleophiles, was investigated in basic media at 25 degrees C in water containing 2% 1,4-dioxane. In the reactions with HO(-) and HOO(-) quant
Autor:
Elba I. Buján, Natalia M. Rougier, Raquel V. Vico, Dyanne L. Cruickshank, Susan A. Bourne, Mino R. Caira, Rita H. de Rossi
Publikováno v:
Carbohydrate Research. 345:141-147
The X-ray crystal structures and thermal stabilities of the inclusion complexes formed between the organophosphate insecticide fenitrothion [O,O-dimethyl O-(3-methyl-4-nitrophenyl) phosphorothioate] and the host compounds TRIMEA and TRIMEB (permethyl
Autor:
Raquel V. Vico, Rita H. de Rossi, Mino R. Caira, Susan A. Bourne, Elba I. Buján, Natalia M. Rougier, Dyanne L. Cruickshank
Publikováno v:
Beilstein Journal of Organic Chemistry
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 106-117 (2013)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 106-117 (2013)
An anhydrous 1:1 crystalline inclusion complex between the organophosphorus insecticide fenitrothion [O,O-dimethyl O-(3- methyl-4-nitrophenyl)phosphorothioate] and the host compound heptakis(2,6-di-O-methyl)-β-cyclodextrin (DIMEB) was prepared and i
Autor:
Dyanne L. Cruickshank, Elba I. Buján, Rita H. de Rossi, Mino R. Caira, Susan A. Bourne, Raquel V. Vico, Natalia M. Rougier
Publikováno v:
Carbohydrate research. 346(2)
The hydrolysis reaction of fenitrothion was studied in water containing 2% dioxane and in the presence of native cyclodextrins (α-, β- and γ-CD) and two commercially available modified derivatives, namely, permethylated β- and α-cyclodextrin (TR
Autor:
Rita H. de Rossi, Mino R. Caira, Natalia M. Rougier, Vincent J. Smith, Mariana A. Fernández, Elba I. Buján, Susan A. Bourne
We report the formation of inclusion complexes between the phenylurea herbicide metobromuron [3-(p-bromophenyl)-1-methoxy-1-methylurea] and β- and γ-cyclodextrin in the solid state. Formation of crystalline inclusion complexes by the kneading metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05fdf9ddc22b606f22b87946a1f7a309
https://www.sciencedirect.com/science/article/abs/pii/S0008621509004029
https://www.sciencedirect.com/science/article/abs/pii/S0008621509004029