01527nas a2200217   4500008004100000245014400041210006900185260000800254300001200262490000800274520077600282653001601058653001301074653001401087653001501101653001001116100001501126700001901141700001901160856013001179       2017                        eng d00aManganese incorporated on glucose as an efficient catalyst for the synthesis of adipic acid using molecular O<inf>2</inf> in aqueous medium0 aManganese incorporated on glucose as an efficient catalyst for t  cSEP  a122-1250 v5463 aA new manganese incorporated on glucose catalyst Mn@CC-SO3H-NH2 was synthesized and well characterized using FT-IR, PXRD, EDAX, SEM, TEM, [13] C cross-polarization NMR and BET analysis. The catalyst thus synthesized was studied for its utility in the synthesis of industrially important chemical adipic acid starting from readily available cyclohexanone using molecular O2 as a source. Adipic acid was obtained in maximum yield of 82% using Mn@CC-SO3H-NH2 catalyst in water as a solvent. The catalyst was easily recovered and reused for minimum five runs without any significant loss in the yield of products. Using molecular O2 as an oxidant and water as a solvent, the reaction is very important from green chemistry perspectives and can also be industrially feasible. 10aAdipic Acid10aCatalyst10amanganese10arecyclable10aWater1 aNale, S.D.1 aRathod, P., V.1 aJadhav, V., H.  uhttps://library.ncl.res.in/content/manganese-incorporated-glucose-efficient-catalyst-synthesis-adipic-acid-using-molecular-o201424nas a2200157   4500008004100000245013300041210006900174260000800243300001200251490000600263520081300269100001901082700001701101700001901118856012901137       2017                        eng d00aMetal free acid base catalyst in the selective synthesis of 2,5-diformylfuran from hydroxynnethylfurfural, fructose, and glucose0 aMetal free acid base catalyst in the selective synthesis of 25di  cJAN  a701-7070 v53 aA novel metal free acid-base (CC-SO3H-NH2) catalyst was synthesized by introducing acidic -SO3H, -COOH, and silyloxypropylamine (-OSiCH2CH2CH2NH2) functional groups on glucose derived carbocatalyst. The catalyst was characterized by Fourier transform infrared (FTIR), powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) analyses. Superior catalytic activity was shown by the catalyst toward one-pot synthesis of DFF using molecular oxygen as the sole oxidant. The catalyst was found to be highly selective in synthesis of 2,5-diformylfuran (DFF) from hydroxymethylfurfural (HMF), fructose, and, more importantly, from glucose with excellent yields. Moreover, the catalyst was easily recycled and reused without any significant loss in its catalytic activity.1 aRathod, P., V.1 aNale, S., D.1 aJadhav, V., H.  uhttps://library.ncl.res.in/content/metal-free-acid-base-catalyst-selective-synthesis-25-diformylfuran-hydroxynnethylfurfural01210nas a2200145   4500008004100000245009000041210006900131260000800200300001400208490000700222520068400229100001900913700001700932856011500949       2017                        eng d00aPalladium incorporated on carbonaceous catalyst for Suzuki coupling reaction in water0 aPalladium incorporated on carbonaceous catalyst for Suzuki coupl  cMAR  a1006-10090 v583 aA new palladium incorporated carbonaceous catalyst Pd@CC SO3H -NH2 was synthesized by introducing palladium on glucose derived carbocatalyst. The catalyst was well characterized and was used for the Suzuki coupling of phenyl boronic acid with different aryl halides under aqueous conditions. This green methodology represents a ligand free, cost-effective and operationally convenient method for the synthesis of a variety of biaryl's under the conditions that are tolerant for a broad range of functional groups with good to excellent yields. Moreover, the catalyst could be easily recycled and reused at least five times without any significant loss of its catalytic activity. 1 aRathod, P., V.1 aJadhav, V.H.  uhttps://library.ncl.res.in/content/palladium-incorporated-carbonaceous-catalyst-suzuki-coupling-reaction-water