Zobrazeno 1 - 10
of 10
pro vyhledávání: '"M. M. Suni"'
Publikováno v:
Designed Monomers and Polymers. 6:81-89
Polystyrene-supported β-diketone-linked palladium complexes on refluxing with olefins at 70°C in a methanol-water medium for 10 h afforded carbonyl compounds. The course of the reaction was influenced by the degree of cross-linking of the polymer m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::274f39bf2ce23e5dfac0e1472c0a8dbc
https://doi.org/10.1163/156855503321127556
https://doi.org/10.1163/156855503321127556
Publikováno v:
Journal of Chemical Sciences. 114:481-486
Poly(methyl methacrylate)-supportedβ-diketone-linked palladium complexes on refluxing with olefins at 70°C in methanol-water medium for 10 h afforded carbonyl compounds. The course of the reaction was found to be influenced by the degree of cross-l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de82747bcc13fd8781ab456682796a78
https://doi.org/10.1007/bf02704191
https://doi.org/10.1007/bf02704191
Publikováno v:
Tetrahedron. 57:2003-2009
Synthesis of a range of 1,2,4-triazolin-5-ones has been carried out by thermally induced cyclization of 1-aryl/alkyl-2-alkyl isothiobiureas 4. The required isothiobiureas were generated in situ by the reaction of alkyl halides with 1-aryl/alkyl-2-thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7705102c4d86e4b0f40dc203a1141be
https://doi.org/10.1016/s0040-4020(01)00018-7
https://doi.org/10.1016/s0040-4020(01)00018-7
Publikováno v:
Synthetic Communications. 31:1599-1605
Reaction of 1-aryl/ alkyl-6-phenyl-2-thiobiureas 1 with BnCl and BuI in neutral medium at reflux temperature resulted in the formation of the S-alkylated isothiobiureas 2 and 1,2,4-triazolin-5-one derivatives 3. A convenient route to 2 is also report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a8bfd3c53b25eb1b4cd0adb0cc0c68e
https://doi.org/10.1081/scc-100104074
https://doi.org/10.1081/scc-100104074
Publikováno v:
Synlett. 2001:0409-0411
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::047c09adc9b516b4fbab3c4d0e18b5b9
https://doi.org/10.1055/s-2001-11399
https://doi.org/10.1055/s-2001-11399
Publikováno v:
Tetrahedron Letters. 42:97-99
1-Alkyl-2-thiobiureas on reaction with α-haloketones such as p -methoxyphenacyl bromide, p -methylphenacyl bromide, p -chlorophenacyl bromide and phenacyl bromide, were found to afford semicarbazonothiazolines in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::604e8e03208ac7099c3b8f9ac3d01da4
https://doi.org/10.1016/s0040-4039(00)01893-1
https://doi.org/10.1016/s0040-4039(00)01893-1
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16e88a11c539707742d2b6624b61fd9e
https://doi.org/10.1002/chin.200128131
https://doi.org/10.1002/chin.200128131
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdff79fa5af020135c04c7d334a5453b
https://doi.org/10.1002/chin.200133055
https://doi.org/10.1002/chin.200133055
Publikováno v:
ChemInform. 32
Reaction of 1-aryl/ alkyl-6-phenyl-2-thiobiureas 1 with BnCl and BuI in neutral medium at reflux temperature resulted in the formation of the S-alkylated isothiobiureas 2 and 1,2,4-triazolin-5-one derivatives 3. A convenient route to 2 is also report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f95f32e159515e76b60a5569ed3b4a60
https://doi.org/10.1002/chin.200144141
https://doi.org/10.1002/chin.200144141
Publikováno v:
ChemInform. 32
1-Alkyl-2-thiobiureas on reaction with α-haloketones such as p -methoxyphenacyl bromide, p -methylphenacyl bromide, p -chlorophenacyl bromide and phenacyl bromide, were found to afford semicarbazonothiazolines in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4acce8d3a0445eab35ff2ad5619b146
https://doi.org/10.1002/chin.200112135
https://doi.org/10.1002/chin.200112135