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Manuscript title: Highly Selective Synthesis of Seven-Membered Azaspiro Compounds by a Rh(I)-Catalyzed Cycloisomerization/Diels–Alder Cascade of 1,5-Bisallenes

Journal: J. Org. Chem.

DOI: 10.1021/acs.joc.2c00065

Full metadata record
DC FieldValueLanguage
dc.contributor.authorvila, jordi-
dc.coverage.spatialES Girona-
dc.date.accessioned2021-12-15T14:02:02Z-
dc.date.available2022-03-16T12:08:53Z-
dc.date.created2021-12-15T15:02:00.7+01:00-
dc.date.issued2021-12-15T15:02:00.7+01:00-
dc.identifier.urihttps://iochem.udg.edu:8443/browse/handle/100/3608-
dc.descriptionClosed-shell TS for the approximation 1B endo-
dc.publisherUdG-
dc.relationOriginal title: Highly Selective Synthesis of Seven-Membered Azaspiro Compounds by a Rh(I)-Catalyzed Cycloisomerization/Diels–Alder Cascade of 1,5-Bisallenes DOI: 10.1021/acs.joc.2c00065 Journal: J. Org. Chem.*
dc.relation.ispartofhttp://dx.doi.org/10.19061/iochem-bd-4-37-
dc.relation.urihttp://dx.doi.org/10.1021/acs.joc.2c00065*
dc.rightsCC BY 4.0 (c) UdG, 2021-
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectstepwise-
dc.subjectCycloaddition-
dc.subjectRhodium-
dc.subjectSpiro compounds-
dc.subjectbiradical-
dc.subjectDiels–Alder reaction-
dc.titleTS(1Bendo)-
dc.typedataset-
dc.date.updated2021-12-15T14:02:02Z-
cml.program.nameGaussianen
cml.program.version16en
cml.program.otherES64L-G16RevA.03en
cml.methodRB3LYPen
cml.basissetCC-PVTZen
cml.multiplicity1en
cml.spintypeRestricteden
cml.shelltypeCloseden
cml.charge0en
cml.energy.value-1769.7252675en
cml.energy.unitsEhen
cml.formula.genericC30H40O8en
cml.calculationtypeSingle point Structureen
cml.hassolventtrueen
cml.hasvibrationalfrequenciesfalseen
cml.numberofjobs1en
cml.hasmolecularorbitalsfalseen
Appears in Collections:Stepwise_vs_concerted_Diels-Alder - DOI: 10.19061/iochem-bd-4-37



Please use this identifier to cite or link to this item: https://iochem.udg.edu:8443/browse/handle/100/3608

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