2019
DOI: 10.1016/j.ccr.2018.12.004
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Recent advances in the catalytic oxidation of alkene and alkane substrates using immobilized manganese complexes with nitrogen containing ligands

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Cited by 60 publications
(20 citation statements)
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“…16 Definitively, these are just a few instances amongst the plethora of organic transformations catalysed by manganese that have been reported in the last lustrum. [17][18][19][20][21][22][23][24][25][26] Encouraged by our interests in the unravelling of the mechanistic aspects in the catalytic chemistry of manganese, [27][28][29][30] the recent work by Milstein et al, 31 reporting for first-time a manganese-catalysed coupling of alcohols and hydrazone to form alkenes, caught our attention. As an alternative to the classical approaches for the synthesis of olefins from carbonyl compounds (such as Wittig, 32 Peterson, 33 or Julia 34 olefinations), Milstein and co-workers offer an unprecedented base-and waste-free procedure for the direct transformation of alcohols into alkenes.…”
Section: Introductionmentioning
confidence: 99%
“…16 Definitively, these are just a few instances amongst the plethora of organic transformations catalysed by manganese that have been reported in the last lustrum. [17][18][19][20][21][22][23][24][25][26] Encouraged by our interests in the unravelling of the mechanistic aspects in the catalytic chemistry of manganese, [27][28][29][30] the recent work by Milstein et al, 31 reporting for first-time a manganese-catalysed coupling of alcohols and hydrazone to form alkenes, caught our attention. As an alternative to the classical approaches for the synthesis of olefins from carbonyl compounds (such as Wittig, 32 Peterson, 33 or Julia 34 olefinations), Milstein and co-workers offer an unprecedented base-and waste-free procedure for the direct transformation of alcohols into alkenes.…”
Section: Introductionmentioning
confidence: 99%
“…Then addition of H 2 O 2 generates the active grafted [(tmtacn)Mn III (µ‐O)(µ‐RCOO) 2 Mn III (tmtacn)] 2+ species. [ 48 ] Careful spectroscopic analyses confirmed that the Mn III /Mn III dimer was fixed onto the acid‐functionalized silica surface. This in situ anchored catalyst was then evaluated in the oxidation of cyclooctene.…”
Section: Manganese‐mediated Syn‐dihydroxylationmentioning
confidence: 99%
“…In past years, scientists utilized various metals such as Pd, Mn, Mo, Se, Fe, etc. for the effective oxidation of alkenes [23][24][25][26][27][28]. The aforementioned results showed that new protocols and mechanisms of these transformations have been developed in past decades.…”
Section: Introductionmentioning
confidence: 99%