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TABLE 7 : CUSTOMERS'OPINION NEED FOR RECOMMENDATION Need for recommendation Needed Not needed TotalNo. of Respondents205575Percentage to total2773100 Source: Primary dataJ. VIMAL PRIYANV. KARTHIHAISELVI
2-Benzylindane radical cations in the gas phase (Part II): Substituent effects on regio- and stereoselective progressive hydrogen scrambling occurring prior to unimolecular fragmentationdoi:10.1016/j.ijms.2016.05.020Dietmar KuckHans-Friedrich Grützmacher...
2-Benzylindane radical cations in the gas phase (Part I): Substituent effects on a stereoselective McLafferty reaction and related hydrogen transfer processesdoi:10.1016/j.ijms.2016.05.021Hans-Friedrich GrützmacherDietmar KuckElsevier
In the present and in the preceding article, the unimolecular fragmentation of the radical cations of 2‐benzylindane and eleven derivatives bearingmeta- orpara-substituents at the benzylic moiety have been studied with respect to the hydrogen exchange that precedes their fragmentation by the Mc...
2-Benzylindane radical cations in the gas phase (Part I): Substituent effects on a stereoselective McLafferty reaction and related hydrogen transfer processesMcLafferty reactionSubstituent effectsDistonic ionsHydrogen transferProton affinityipso-Protonation...
Vincent GervatFrançoise FournierMarie-Claude PerlatJean-Claude TabetJournal of the American Society for Mass SpectrometryGervat, V., Fournier, F., Perlat, M.C., Tabet, J.C.: Ion–molecule reactions in the gas phase. Part xxii. Reactivity of the cis- and trans-indanediols with dimethyl...
Esters 4 and 5 were reduced in ethanol with hydrogen gas on Pd/C catalyst. Resulting amines 6 and 7 were azocoupled (NaNO22/TsOH ) with phenol in water/MeCN mixture (setup similar to black quencher synthesis described in [28]) to yield target compounds 4-aphin and 6-aphin. Figure 2...