Asymmetric carbon-carbon bond formation under continuous-flow conditions with chiral heterogeneous catalysts.
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Building Bridges: Biocatalytic C–C-Bond Formation toward Multifunctional ProductsFlow "Fine" Synthesis: High Yielding and Selective Organic Synthesis by Flow MethodsStrategic Application of Residence-Time Control in Continuous-Flow ReactorsHighly functionalized biaryls via Suzuki-Miyaura cross-coupling catalyzed by Pd@MOF under batch and continuous flow regimes.A polystyrene-supported 9-amino(9-deoxy)epi quinine derivative for continuous flow asymmetric Michael reactions.Continuous flow of nitroso Diels-Alder reaction.Enantioselective Synthesis of Carbo- and Heterocycles through a CuH-Catalyzed Hydroalkylation Approach.Development of an Intermittent-Flow Enantioselective Aza-Henry Reaction Using an Arylnitromethane and Homogeneous Brønsted Acid-Base Catalyst with Recycle.Accessing new chemical entities through microfluidic systems.A catalytic chiral gel microfluidic reactor assembled via dynamic covalent chemistry.Chirality-driven wettability switching and mass transfer.Investigation of a lithium-halogen exchange flow process for the preparation of boronates by using a cryo-flow reactor.Self-Assembled Nanocomposite Organic Polymers with Aluminum and Scandium as Heterogeneous Water-Compatible Lewis Acid Catalysts.1,6-Conjugate addition of zinc alkyls to para-quinone methides in a continuous-flow microreactor.Stereoselective Reduction of Imines with Trichlorosilane Using Solid-Supported Chiral Picolinamides.A fully recyclable heterogenized Cu catalyst for the general carbene transfer reaction in batch and flow.Induced Chirality in a Metal-Organic Framework by Postsynthetic Modification for Highly Selective Asymmetric Aldol ReactionsContinuous-Flow Asymmetric Hydrogenation of an Enol Ester by using Supercritical Carbon Dioxide: Ionic Liquids versus Supported Ionic Liquids as the Catalyst MatrixSynthesis in mesoreactors: Ru(porphyrin)CO-catalyzed aziridination of olefins under continuous flow conditions
P2860
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P2860
Asymmetric carbon-carbon bond formation under continuous-flow conditions with chiral heterogeneous catalysts.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Asymmetric carbon-carbon bond ...... hiral heterogeneous catalysts.
@en
Asymmetric carbon-carbon bond ...... hiral heterogeneous catalysts.
@nl
type
label
Asymmetric carbon-carbon bond ...... hiral heterogeneous catalysts.
@en
Asymmetric carbon-carbon bond ...... hiral heterogeneous catalysts.
@nl
prefLabel
Asymmetric carbon-carbon bond ...... hiral heterogeneous catalysts.
@en
Asymmetric carbon-carbon bond ...... hiral heterogeneous catalysts.
@nl
P2093
P2860
P356
P1476
Asymmetric carbon-carbon bond ...... hiral heterogeneous catalysts.
@en
P2093
Shū Kobayashi
Takanori Ishiwata
Tetsu Tsubogo
P2860
P304
P356
10.1002/ANIE.201210066
P407
P577
2013-05-29T00:00:00Z