01195nas a2200145   4500008004100000245009100041210006900132260000800201300001600209490000600225520065900231100002000890700001900910856012000929       2016                        eng d00aFacile O-glycosylation of glycals using Glu-Fe3O4-SO3H, a magnetic solid acid catalyst0 aFacile Oglycosylation of glycals using GluFe3O4SO3H a magnetic s  cAUG  a30846-308510 v63 aA new glucose derived magnetic solid acid catalyst (Glu-Fe3O4-SO3H) was synthesized in a convenient and ecofriendly manner and well characterized using FTIR, PXRD, EDAX, SEM, and XPS which showed the presence of Fe3O4 embedded on the surface of the catalyst along with -SO3H, -OH and -COOH functional groups. This new heterogeneous catalyst was studied for synthesis of 2-deoxy galactosides/glucosides with good yields and selectivity. Moreover, the catalyst can be easily separated from the reaction with an external magnetic force and reused for a minimum of four times without any significant decrease in the yields of the products after every recycle1 aThombal, R., S.1 aJadhav, V., H.  uhttps://library.ncl.res.in/content/facile-o-glycosylation-glycals-using-glu-fe3o4-so3h-magnetic-solid-acid-catalyst01062nas a2200157   4500008004100000245005400041210005300095260000800148300001400156490000800170520060500178100001700783700001900800700000500819856008000824       2016                        eng d00aSynthesis of fuel intermediates from HMF/fructose0 aSynthesis of fuel intermediates from HMFfructose  cOCT  a1984-19900 v1463 aAlkylation of toluene, anisole and mesitylene with HMF and fructose is reported using Glu–Fe3O4–SO3H solid acid catalyst. HMF was found to alkylate toluene, anisole and mesitylene in high yields and high selectivity under solvent free conditions. Polyalkylation and self etherification of HMF was not observed. The alkylated product on hydrodeoxygenation forms liquid alkanes of different chain lengths which have properties of transportation fuels or diesel fuels. The catalyst was easily recoverable and reusable minimum 5 times to achieve good yields and high selectivity of alkylated product.1 aNale, S., D.1 aJadhav, V., H.1 a  uhttps://library.ncl.res.in/content/synthesis-fuel-intermediates-hmffructose00932nas a2200145   4500008004100000245006000041210005900101260000800160300001400168490000700182520046900189100001700658700001900675856009200694       2016                        eng d00aSynthesis of tyrosyl-DNA phosphodiesterase i inhibitors0 aSynthesis of tyrosylDNA phosphodiesterase i inhibitors  cJUN  a2652-26540 v573 aThe first report for the synthesis of tyrosyl-DNA phosphodiesterase I inhibitors 3,4-dimethoxyphenol-1-β-d-(6′-O-galloyl)glucopyranoside 3 and 3-(4-hydroxy-3-methoxyphenyl)propane-1,2-diol 2-β-d-(6′-O-galloyl) glucopyranoside 5 has been accomplished starting from readily available d-glucose as a starting material. An efficient and general approach has been reported for the synthesis of compounds 3 and 5 with an overall yield of 26% and 27%, respectively.1 aNale, S., D.1 aJadhav, V., H.  uhttps://library.ncl.res.in/content/synthesis-tyrosyl-dna-phosphodiesterase-i-inhibitors01527nas 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-hydroxynnethylfurfural