Otte, Matthias

[["dc.bibliographiccitation.firstpage","4755"],["dc.bibliographiccitation.issue","20"],["dc.bibliographiccitation.journal","ChemCatChem"],["dc.bibliographiccitation.lastpage","4760"],["dc.bibliographiccitation.volume","10"],["dc.contributor.author","Li, Jing"],["dc.contributor.author","Lutz, Martin"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2021-04-29T10:11:39Z"],["dc.date.available","2021-04-29T10:11:39Z"],["dc.date.issued","2018-10-23"],["dc.description.abstract","Trioxo-rhenium complexes are well known catalysts for the deoxydehydration (DODH) of vicinal diols (glycols). In this work, we report on the DODH of diols and biomass-derived polyols using CpttReO3 as a new catalyst (Cptt=1,3-di-tert-butylcyclopentadienyl). The DODH reaction was optimized using 2 mol % of CpttReO3 and 3-octanol as both reductant and solvent. The CpttReO3 catalyst exhibits an excellent activity for biomass-derived polyols. Specifically, glycerol is almost quantitatively converted to allyl alcohol and mucic acid gives 75 % of muconates at 91 % conversion. In addition, the loading of CpttReO3 can be reduced to 0.1 mol % to achieve a turn-over number as high as 900 per Re when using glycerol as substrate. Examination of DODH reaction profiles by NMR spectroscopy indicates that catalysis is related to Cp-ligand release, which raises questions on the nature of the actual catalyst."],["dc.identifier.doi","10.1002/cctc.201801151"],["dc.identifier.pmid","31007775"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84577"],["dc.language.iso","en"],["dc.relation.issn","1867-3880"],["dc.title","A Cptt-Based Trioxo-Rhenium Catalyst for the Deoxydehydration of Diols and Polyols"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1319"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","European Journal of Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","1332"],["dc.bibliographiccitation.volume","2016"],["dc.contributor.author","Folkertsma, Emma"],["dc.contributor.author","de Waard, Esther F."],["dc.contributor.author","Korpershoek, Gerda"],["dc.contributor.author","van Schaik, Arnoldus J."],["dc.contributor.author","Solozabal Mirón, Naiara"],["dc.contributor.author","Borrmann, Mandy"],["dc.contributor.author","Nijsse, Sjoerd"],["dc.contributor.author","Moelands, Marcel A. H."],["dc.contributor.author","Lutz, Martin"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Moret, Marc-Etienne"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2021-04-29T10:11:19Z"],["dc.date.available","2021-04-29T10:11:19Z"],["dc.date.issued","2016"],["dc.identifier.doi","10.1002/ejic.201501406"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84572"],["dc.relation.issn","1434-1948"],["dc.title","Mimicry of the 2-His-1-Carboxylate Facial Triad Using Bulky N,N,O-Ligands: Non-Heme Iron Complexes Featuring a Single Facial Ligand and Easily Exchangeable Co-Ligands"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2590"],["dc.bibliographiccitation.issue","15"],["dc.bibliographiccitation.journal","Advanced Synthesis & Catalysis"],["dc.bibliographiccitation.lastpage","2595"],["dc.bibliographiccitation.volume","359"],["dc.contributor.author","Chen, Jianming"],["dc.contributor.author","Lutz, Martin"],["dc.contributor.author","Milan, Michela"],["dc.contributor.author","Costas, Miquel"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2021-04-29T10:11:34Z"],["dc.date.available","2021-04-29T10:11:34Z"],["dc.date.issued","2017"],["dc.identifier.doi","10.1002/adsc.201700239"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84576"],["dc.relation.issn","1615-4150"],["dc.title","Non-Heme Iron Catalysts with a Rigid Bis-Isoindoline Backbone and Their Use in Selective Aliphatic C−H Oxidation"],["dc.type","journal_article"],["dc.type.internalPublication","unknown"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","1657"],["dc.bibliographiccitation.issue","12"],["dc.bibliographiccitation.journal","European Journal of Organic Chemistry"],["dc.bibliographiccitation.lastpage","1661"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Lutz, Martin"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2018-11-07T10:26:02Z"],["dc.date.available","2018-11-07T10:26:02Z"],["dc.date.issued","2017"],["dc.description.abstract","The selective synthesis of purely organic cages with hetero-sequenced functionalized cavities is demonstrated. The strategy to obtain these compounds is based on a stepwise approach using thermodynamically controlled imine condensations. To accomplish this, the amine building blocks carry additional azide groups, which act as masked amines and enable the synthesis of the desired cavities. This approach offers a precise control of interior functionalization, the substitution pattern and the cage size, which is demonstrated by the selective synthesis of four cages. The largest described cage has been investigated towards its ability for guest encapsulation and is able to selectively encapsulate functionalized arenes that offer a matching substitution pattern."],["dc.identifier.doi","10.1002/ejoc.201700106"],["dc.identifier.isi","000397850000012"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42962"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1099-0690"],["dc.relation.issn","1434-193X"],["dc.title","Selective Synthesis of Hetero-Sequenced Aza-Cyclophanes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]