02080nas a2200229   4500008004100000022001400041245007800055210006900133260011100202300001200313490000700325520121200332653001801544653002701562653002701589653002401616653003201640100002101672700002301693700002401716856011001740       2015                        eng d  a1385-272800aTailor made ionic liquids: catalyst and media for organic transformations0 aTailor made ionic liquids catalyst and media for organic transfo  aEXECUTIVE STE Y-2, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATESbBENTHAM SCIENCE PUBL LTDcFEB  a728-7420 v193 a<p>Ionic liquids are considered as one of the safe, green and environmentally benign solvents/catalysts for many organic reactions. Particularly, imidazolium based ionic liquids attracted much attention in basic as well as applied research. The major role of these ionic liquids is the replacement of the existing corrosive solvents, which are largely used in most of the organic processes and make these processes more eco-friendly. Recent report reveals the importance of imidazolium based ionic liquids, supported on silica gel or polystyrene in catalysis. The solid supports have well versed properties such as easy anchoring of ionic liquid, chemically and mechanically very stable and inert in nature. These ionic liquids can be tailored either by covalent attachment or simple deposition of the ionic liquid on the surface of the support. Both approaches showed enhanced reactivity and selectivity for various reactions. In this review, we made an attempt to review the recent reports related to synthesis and applications of tailor made ionic liquids and their use as catalyst in Aldol, Friedel-Crafts alkylation, hydroformylation, nucleophilic substitution and biomass transformation reactions.</p>10aGreen solvent10aheterogeneous catalyst10aorganic transformation10asustainable process10atask-specific ionic liquids1 aChandra, Prakash1 aShinde, Sandip, S.1 aBiradar, Ankush, V.  uhttps://library.ncl.res.in/content/tailor-made-ionic-liquids-catalyst-and-media-organic-transformations-001579nas a2200229   4500008004100000022001400041245015900055210006900214260000800283300001400291490000700305520072400312653004101036653001801077653003601095653001501131653001301146100002201159700002101181700002101202856012601223       2020                        eng d  a0922-616800aNovel synthesis of 3-((benzo[d]thiazol-2-ylamino)(phenyl)methyl)-4-hydroxy-1-methylquinol in-2(1H)-one via consecutive C-C and C-N bond formation in water0 aNovel synthesis of 3benzodthiazol2ylaminophenylmethyl4hydroxy1me  cAUG  a3801-38150 v463 a<p>A simple, efficient, and eco-friendly protocol has been developed for the synthesis of novel 3-((benzo[d]thiazol-2-ylamino)(4-methoxyphenyl)methyl)-4-hydroxy-1-met hylquinolin-2(1H)-one derivatives using a one-pot C-C and C-N bond forming strategy from the reaction of 4-hydroxy-1-methylquinolin-2(1H)-one, 2-aminobenzothiazole and aromatic aldehydes in aqueous solvent without using any metal catalyst. Several advantages of this protocol include its operational simplicity, short reaction time, mild reaction condition, efficient utilization of all the reactants, wide functional group tolerance, using water as an environmentally friendly solvent and non-chromatographic purification procedure. [GRAPHICS] .</p>
10a4-Hydroxy-1-methylquinolin-2(1H)-one10aGreen solvent10aMulticomponent reactions (MCRs)10aQuinolines10aThiazole1 aYadav, Maruti, B.1 aVagh, Sandip, S.1 aJeong, Yeon, Tae  uhttps://library.ncl.res.in/content/novel-synthesis-3-benzodthiazol-2-ylaminophenylmethyl-4-hydroxy-1-methylquinol-21h-one