2015
DOI: 10.1039/c5ra10730j
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N,2-Dibromo-6-chloro-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazine-7-sulfonamide 1,1-dioxide: an efficient and homogeneous catalyst for one-pot synthesis of 4H-pyran, pyranopyrazole and pyrazolo[1,2-b]phthalazine derivatives under aqueous media

Abstract: An international journal to further the chemical sciencesRSC Advances is an international, peer-reviewed, online journal covering all of the chemical sciences, including interdisciplinary fields.The criteria for publication are that the experimental and/or theoretical work must be high quality, well conducted and demonstrate an advance by adding to the development of the field . It is essential that all research work reported in RSC Advances is well-carried out and wellcharacterised. There should be enough sup… Show more

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Cited by 59 publications
(24 citation statements)
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“…Khazaei reported an eco‐friendly one‐pot method for the synthesis of spiro‐oxindoles derivatives in aqueous medium catalyzed by N ,2‐Dibromo‐6‐chloro‐3,4‐dihydro‐2 H ‐benzo[ e ][1,2,4]thiadiazine‐7‐sulfonamide 1,1‐dioxide (DCDBTSD) (Scheme ). Spiro‐pyran‐oxindoles ( 60 , 61 ), as well as spiro‐pyrazoline‐oxindoles ( 62 ) were synthesized via this one‐pot multicomponent reaction at 80 °C in water.…”
Section: Organic–catalyzed Mcrs Synthesis Of 33′‐spirooxindolesmentioning
confidence: 99%
“…Khazaei reported an eco‐friendly one‐pot method for the synthesis of spiro‐oxindoles derivatives in aqueous medium catalyzed by N ,2‐Dibromo‐6‐chloro‐3,4‐dihydro‐2 H ‐benzo[ e ][1,2,4]thiadiazine‐7‐sulfonamide 1,1‐dioxide (DCDBTSD) (Scheme ). Spiro‐pyran‐oxindoles ( 60 , 61 ), as well as spiro‐pyrazoline‐oxindoles ( 62 ) were synthesized via this one‐pot multicomponent reaction at 80 °C in water.…”
Section: Organic–catalyzed Mcrs Synthesis Of 33′‐spirooxindolesmentioning
confidence: 99%
“…M.p. 253 – 254 °C (: 253 – 254 °C). 1 H‐NMR (300 MHz, (D 6 )DMSO): 2.27 ( s , Me); 4.41 ( s , CH); 7.10 – 7.16 ( m , 4 arom.…”
Section: Experimental Partmentioning
confidence: 99%
“…Chromeno pyrazolo and indazolo phthalazine derivatives constitute a bridgehead hydrazine as a group of nitrogen‐containing heterocyclic compounds, which possess a multiplicity of pharmacological properties including anti‐inflammatory, antimicrobial, antifungal, anticonvulsant, vasorelaxant, antitumor and cardiotonic activities . Due to the large biological activity of phthalazine compounds, number of methods have been reported such as ionic liquids, magnetic nanoparticles, solid supported catalysts, heteropolyacids, β‐cyclodextrin, microwave, sulfonic acid, alumina nanoparticles and p‐TSA …”
Section: Introductionmentioning
confidence: 99%