Asymmetric tandem 1,5-hydride shift/ring closure for the synthesis of chiral spirooxindole tetrahydroquinolines.
about
Organo- and Organometallic-Catalytic Intramolecular [1,5]-Hydride Transfer/Cyclization Process through C(sp(3) )-H Bond Activation.Redox-Annulation of Cyclic Amines and β-Ketoaldehydes.Hydrogen-Atom Transfer Reactions.Intramolecular Redox-Mannich Reactions: Facile Access to the Tetrahydroprotoberberine Core.C-H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds.An Ugi Reaction Incorporating a Redox-Neutral Amine C-H Functionalization StepRedox-Neutral Aromatization of Cyclic Amines: Mechanistic Insights and Harnessing of Reactive Intermediates for Amine α- and β-C-H Functionalization.A tandem annulation with a [1,3]-hydride transfer as the key step leading to isochromans.A catalytic asymmetric construction of a tetrahydroquinoline-based spirooxindole framework via a diastereo- and enantioselective decarboxylative [4+2] cycloaddition.Expedient synthesis of tetrahydroquinoline-3-spirohydantoin derivatives via the Lewis acid-catalyzed tert-amino effect reaction.
P2860
Q38803445-9C69B959-96E9-4CC3-A88D-F455DDE0838FQ38834644-C89B2E2D-4290-435C-AB8F-23B58B846975Q38940195-69E648BF-9045-4FF7-B408-95FA2D7BA3A3Q39530179-E6DB8D5B-958A-4CFE-8DFA-4C087354362EQ41928386-86026579-6FC7-43AB-B05F-486447CE209BQ42154026-EA54DA56-4F31-4F7A-8FBD-07CE20BD0E58Q46586475-91123D3C-A34D-45CF-963D-4A9913C2C07EQ47678204-6D38BA74-C6F0-45A0-84C3-AC5BA97809F1Q53098259-C1E1848A-6854-466F-BA71-67093B3ED8F4Q54573145-9765C669-2593-420E-A436-476CC89C768F
P2860
Asymmetric tandem 1,5-hydride shift/ring closure for the synthesis of chiral spirooxindole tetrahydroquinolines.
description
2014 nî lūn-bûn
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2014年の論文
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2014年学术文章
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name
Asymmetric tandem 1,5-hydride ...... oxindole tetrahydroquinolines.
@en
Asymmetric tandem 1,5-hydride ...... oxindole tetrahydroquinolines.
@nl
type
label
Asymmetric tandem 1,5-hydride ...... oxindole tetrahydroquinolines.
@en
Asymmetric tandem 1,5-hydride ...... oxindole tetrahydroquinolines.
@nl
prefLabel
Asymmetric tandem 1,5-hydride ...... oxindole tetrahydroquinolines.
@en
Asymmetric tandem 1,5-hydride ...... oxindole tetrahydroquinolines.
@nl
P2860
P50
P356
P1476
Asymmetric tandem 1,5-hydride ...... oxindole tetrahydroquinolines.
@en
P2093
P2860
P304
P356
10.1002/CHEM.201404327
P407
P577
2014-11-24T00:00:00Z