Otte, Matthias

[["dc.bibliographiccitation.firstpage","3462"],["dc.bibliographiccitation.issue","21"],["dc.bibliographiccitation.journal","European Journal of Inorganic Chemistry"],["dc.bibliographiccitation.lastpage","3466"],["dc.bibliographiccitation.volume","2015"],["dc.contributor.author","Spannring, Peter"],["dc.contributor.author","Yazerski, Vital A."],["dc.contributor.author","Chen, Jianming"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Weckhuysen, Bert M."],["dc.contributor.author","Bruijnincx, Pieter C. A."],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2021-04-29T10:11:11Z"],["dc.date.available","2021-04-29T10:11:11Z"],["dc.date.issued","2015"],["dc.identifier.doi","10.1002/ejic.201500213"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84570"],["dc.relation.issn","1434-1948"],["dc.title","Regioselective Cleavage of Electron-Rich Double Bonds in Dienes to Carbonyl Compounds with [Fe(OTf)2(mix-BPBP)] and a Combination of H2O2and NaIO4"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["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","4172"],["dc.bibliographiccitation.issue","17"],["dc.bibliographiccitation.journal","Organic Letters"],["dc.bibliographiccitation.lastpage","4175"],["dc.bibliographiccitation.volume","17"],["dc.contributor.author","Vliegenthart, Annette B."],["dc.contributor.author","Welling, Frank A. L."],["dc.contributor.author","Roemelt, Michael"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.contributor.author","Otte, Matthias"],["dc.date.accessioned","2021-04-29T10:11:16Z"],["dc.date.available","2021-04-29T10:11:16Z"],["dc.date.issued","2015-09-04"],["dc.description.abstract","The first shape-persistent macrocycle 1 offering a Brønsted pair functionalized interior is described. Via postcyclization transformation, this heterosequenced compound can be obtained from its corresponding ester 2. The macrocycles differ dramatically in their characteristics such as solubility and appearance. Theoretical investigations suggest that those contrasts might originate from conformational changes due to the formation of a strong O-H-N hydrogen bond in 1."],["dc.identifier.doi","10.1021/acs.orglett.5b01931"],["dc.identifier.pmid","26305263"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84571"],["dc.language.iso","en"],["dc.relation.eissn","1523-7052"],["dc.relation.issn","1523-7060"],["dc.title","Synthesis and Characterization of a Brønsted Pair Functionalized Shape-Persistent Macrocycle"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3714"],["dc.bibliographiccitation.issue","15"],["dc.bibliographiccitation.journal","Organic Letters"],["dc.bibliographiccitation.lastpage","3717"],["dc.bibliographiccitation.volume","18"],["dc.contributor.author","Tiddens, Martine R."],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.contributor.author","Otte, Matthias"],["dc.date.accessioned","2021-04-29T10:11:27Z"],["dc.date.available","2021-04-29T10:11:27Z"],["dc.date.issued","2016"],["dc.description.abstract","A system of three coupled catalytic cycles enabling the one-pot transformation of epoxides to amines via Meinwald rearrangement, imine condensation, and imine reduction is described. This assisted tandem catalysis is catalyzed by B(C6F5)3 resulting in the first tandem Meinwald rearrangement-reductive amination protocol. The reaction proceeds in nondried solvents and yields β-functionalized amines. In particular, β-diarylamines are obtained in high yields."],["dc.identifier.doi","10.1021/acs.orglett.6b01744"],["dc.identifier.pmid","27459685"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/84574"],["dc.language.iso","en"],["dc.relation.eissn","1523-7052"],["dc.relation.issn","1523-7060"],["dc.title","The B(C6F5)3-Catalyzed Tandem Meinwald Rearrangement-Reductive Amination"],["dc.type","journal_article"],["dc.type.internalPublication","no"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2436"],["dc.bibliographiccitation.issue","9"],["dc.bibliographiccitation.journal","Green Chemistry"],["dc.bibliographiccitation.lastpage","2447"],["dc.bibliographiccitation.volume","21"],["dc.contributor.author","Chen, Jianming"],["dc.contributor.author","de Liedekerke Beaufort, Marc"],["dc.contributor.author","Gyurik, Lucas"],["dc.contributor.author","Dorresteijn, Joren"],["dc.contributor.author","Otte, Matthias"],["dc.contributor.author","Klein Gebbink, Robertus J. M."],["dc.date.accessioned","2020-12-10T18:11:23Z"],["dc.date.available","2020-12-10T18:11:23Z"],["dc.date.issued","2019"],["dc.identifier.doi","10.1039/C8GC03857K"],["dc.identifier.eissn","1463-9270"],["dc.identifier.issn","1463-9262"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/73990"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Highly efficient epoxidation of vegetable oils catalyzed by a manganese complex with hydrogen peroxide and acetic acid"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["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"]]