Highly Versatile β-C(sp3)-H Iodination of Ketones Using a Practical Auxiliary.
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Versatile Alkylation of (Hetero)Aryl Iodides with Ketones via β-C(sp3)-H Activation.2-(1-Methylhydrazinyl)pyridine as a reductively removable directing group in a cobalt-catalyzed C(sp2)-H bond alkenylation/annulation cascade.α-Aminoxy-Acid-Auxiliary-Enabled Intermolecular Radical γ-C(sp3 )-H Functionalization of Ketones.Ligand-Enabled γ-C(sp3)-H Activation of Ketones.β C–H di-halogenation via iterative hydrogen atom transfer† †Electronic supplementary information (ESI) available. CCDC 1581032. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8sc01214h.α-Aminoxy-Acid-Auxiliary-Enabled Intermolecular Radical γ-C(sp3 )−H Functionalization of Ketones
P2860
Highly Versatile β-C(sp3)-H Iodination of Ketones Using a Practical Auxiliary.
description
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name
Highly Versatile β-C
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Highly Versatile β-C(sp3)-H Iodination of Ketones Using a Practical Auxiliary.
@en
type
label
Highly Versatile β-C
@nl
Highly Versatile β-C(sp3)-H Iodination of Ketones Using a Practical Auxiliary.
@en
prefLabel
Highly Versatile β-C
@nl
Highly Versatile β-C(sp3)-H Iodination of Ketones Using a Practical Auxiliary.
@en
P2860
P356
P1476
Highly Versatile β-C(sp3)-H Iodination of Ketones Using a Practical Auxiliary.
@en
P2093
P2860
P304
12394-12397
P356
10.1021/JACS.7B06851
P407
P577
2017-08-27T00:00:00Z