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DC FieldValueLanguage
cml.program.nameGaussianen
cml.program.version09en
cml.program.otherEM64L-G09RevD.01en
cml.methodRM062Xen
cml.multiplicity1en
cml.spintypeRestricteden
cml.shelltypeCloseden
cml.charge1en
cml.energy.value-2045.23493578en
cml.energy.unitsEhen
cml.formula.genericC38H46NO3Sien
cml.calculationtypeSingle point Structureen
cml.hassolventtrueen
cml.hasvibrationalfrequenciesfalseen
cml.numberofjobs1en
cml.hasmolecularorbitalsfalseen
cml.formula.smilesCCCCN1CCCC1C(O[Si](C)(C)C)(C1CCCCC1)C1CCCCC1.CC1CCCCC1C(O)C1CCCCC1en
dc.contributor.authorFernández, Víctor-
dc.contributor.otherInstitute of Chemical Research of Cataloniaen
dc.date.accessioned2017-02-03T09:50:42Z-
dc.date.accessioned2019-05-04T13:12:55Z-
dc.date.available2017-02-03T09:50:42Z-
dc.date.available2019-05-04T13:12:55Z-
dc.date.created2017-02-03T10:50:40.833+01:00-
dc.date.issued2017-02-03T10:50:40.833+01:00-
dc.identifier.urihttps://www.iochem-bd.org//handle/10/8768-
dc.descriptionTS1-H2O solvent-
dc.publisherInstitute of Chemical Research of Catalonia-
dc.relationOriginal title: Light-Driven Enantioselective Organocatalytic beta-Benzylation of Enals DOI: 10.1002/anie.201612159 Journal: Angew. Chem. Int. Ed.-
dc.relation.ispartofhttp://dx.doi.org/10.19061/iochem-bd-1-28-
dc.relation.urihttp://dx.doi.org/10.1002/anie.201612159-
dc.rightsCC BY 4.0 (c) Institute of Chemical Research of Catalonia, 2017-
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.titleTS1-H2O_solvent-
dc.typedataset-
dc.date.updated2017-02-03T09:50:42Z-
Appears in Collections:Michael_addition_vs_Diels_Alder

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atk3mic_mod_ts_1_pc_ts_sp.in3.76 kBDownload
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Manuscript title: Light-Driven Enantioselective Organocatalytic beta-Benzylation of Enals

Journal: Angew. Chem. Int. Ed.

DOI: 10.1002/anie.201612159



Please use this identifier to cite or link to this item: https://www.iochem-bd.org//handle/10/8768

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