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DC FieldValueLanguage
cml.program.nameGaussianen
cml.program.version09en
cml.program.otherEM64L-G09RevD.01en
cml.methodRM06en
cml.multiplicity1en
cml.spintypeRestricteden
cml.shelltypeCloseden
cml.charge0en
cml.energy.value-1111.20468322en
cml.energy.unitsEhen
cml.formula.genericC19H30N4O2en
cml.calculationtypeSingle point Structureen
cml.hassolventtrueen
cml.hasvibrationalfrequenciestrueen
cml.numberofjobs1en
cml.hasmolecularorbitalsfalseen
cml.formula.smilesOCCCCCC(O)NC1CCCCC1.C1CNC2NCCCN2C1en
dc.contributor.authorBandeira, Nuno-
dc.contributor.otherInstitute of Chemical Research of Cataloniaen
dc.date.accessioned2016-11-25T11:33:35Z-
dc.date.accessioned2019-05-04T08:46:45Z-
dc.date.available2017-04-07T10:21:24Z-
dc.date.available2019-05-04T08:46:45Z-
dc.date.created2016-11-25T12:33:34.233+01:00-
dc.date.issued2016-11-25T12:33:34.233+01:00-
dc.identifier.urihttps://www.iochem-bd.org//handle/10/326-
dc.descriptionTS#2-
dc.publisherInstitute of Chemical Research of Catalonia-
dc.relationOriginal title: Metal-Free Synthesis of N-Aryl Amides using Organocatalytic Ring-Opening Aminolysis of Lactones DOI: 10.1002/cssc.201700415 Journal: ChemSusChem*
dc.relation.ispartofhttp://dx.doi.org/10.19061/iochem-bd-1-21-
dc.rightsCC BY 4.0 (c) Institute of Chemical Research of Catalonia, 2016-
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.title/7_membered_lactone/Solvated_Single_points TS_2-
dc.typedataset-
dc.date.updated2016-11-25T11:33:35Z-
Appears in Collections:Aromatic_Amination_of_Lactones

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Manuscript title: Metal-Free Synthesis of N-Aryl Amides using Organocatalytic Ring-Opening Aminolysis of Lactones

Journal: ChemSusChem

DOI: 10.1002/cssc.201700415



Please use this identifier to cite or link to this item: https://www.iochem-bd.org//handle/10/326

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