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BielawskiChristopher W

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N,N '-Diamidocarbenes Facilitate Selective C-H Insertions and Transfer Hydrogenations

Author(s)
Moerdyk, Jonathan P.Bielawski, Christopher W.
Issued Date
2013-10
DOI
10.1002/chem.201302691
URI
https://scholarworks.unist.ac.kr/handle/201301/31479
Fulltext
https://onlinelibrary.wiley.com/doi/full/10.1002/chem.201302691
Citation
CHEMISTRY-A EUROPEAN JOURNAL, v.19, no.44, pp.14773 - 14776
Abstract
C-H bound: Diamidocarbenes were found to facilitate highly selective CH bond activation in hydrocarbons containing benzylic, allylic, or α‐carbonyl positions. Mechanistic studies showed a preference for intramolecular CH insertion for CH bonds at more substituted carbon atoms, whereas intermolecular insertions were enabled by relatively electron‐deficient substrates. The diamidocarbenes also promoted metal‐ and additive‐free transfer hydrogenations.
Publisher
WILEY-V C H VERLAG GMBH
ISSN
0947-6539
Keyword (Author)
carbenesC-H activationdehydrogenationdiamidocarbenetransfer hydrogenation
Keyword
N-HETEROCYCLIC CARBENEFUNCTIONALIZATION/COPE REARRANGEMENTCATALYTIC FUNCTIONALIZATIONACTIVATIONBONDSCYCLOADDITIONVERSATILEBACKBONE

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