2021
DOI: 10.1002/cssc.202102619
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Cover Feature: Highly Selective Hydrogenative Conversion of Nitriles into Tertiary, Secondary, and Primary Amines under Flow Reaction Conditions (ChemSusChem 2/2022)

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“…On the other hand, both substrates in solutions and gaseous molecules can directly and efficiently interact with heterogeneous catalysts under flow conditions; therefore reactions can be performed under mild conditions, and significant rate acceleration was observed in some cases by overcoming the problem of mass transfer . By making use of this unique nature of flow reactions, continuous-flow hydrogenations of various kinds of functional groups have been developed until now. Reported examples are, however, limited to only simple functional group interconversions and (hetero)­arene hydrogenations, and continuous-flow enantioselective hydrogenative C−C bond forming reactions, which can construct chiral molecular scaffolds, remain unexplored.…”
mentioning
confidence: 99%
“…On the other hand, both substrates in solutions and gaseous molecules can directly and efficiently interact with heterogeneous catalysts under flow conditions; therefore reactions can be performed under mild conditions, and significant rate acceleration was observed in some cases by overcoming the problem of mass transfer . By making use of this unique nature of flow reactions, continuous-flow hydrogenations of various kinds of functional groups have been developed until now. Reported examples are, however, limited to only simple functional group interconversions and (hetero)­arene hydrogenations, and continuous-flow enantioselective hydrogenative C−C bond forming reactions, which can construct chiral molecular scaffolds, remain unexplored.…”
mentioning
confidence: 99%