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An Efficient Partial Reduction of α,β‐Unsaturated Esters Using DIBAL‐H in Flow

https://doi.org/10.1002/ejoc.201402675
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Lithium diisobutyl-t-butoxyaluminum hydride, a new and efficient reducing agent for the conversion of esters to aldehydes
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Spiruchostatins A and B, novel gene expression-enhancing substances produced by Pseudomonas sp.
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Reduction of esters of carboxylic acids into aldehydes with diisobutylaluminium hydride
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Dihydro-1,3-oxazines. XV. Two-carbon homologation of alkyl halides to aldehydes using a novel ketene N,O-acetal
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Carbon Dioxide-Mediated Catalytic Rearrangement of Propargyl Alcohols into α,β-Unsaturated Ketones
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Remarkable Effect of Bimetallic Nanocluster Catalysts for Aerobic Oxidation of Alcohols: Combining Metals Changes the Activities and the Reaction Pathways to Aldehydes/Carboxylic Acids or Esters
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Emission Wavelength Prediction of a Full-Color-Tunable Fluorescent Core Skeleton, 9-Aryl-1,2-dihydropyrrolo[3,4-b]indolizin-3-one
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Catalytic Enantioselective Dibromination of Allylic Alcohols
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Structure and Activity of Largazole, a Potent Antiproliferative Agent from the Floridian Marine Cyanobacterium Symploca sp.
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Preparation, Structure, and Reactivity of Nonstabilized Organoiron Compounds. Implications for Iron-Catalyzed Cross Coupling Reactions
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Base-Induced Mechanistic Variation in Palladium-Catalyzed Carbonylation of Aryl Iodides
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Total Synthesis of the Antitumor Depsipeptide FR-901,228
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Spectrophotometric Studies of Some 2,4-Dinitrophenylhydrazones. IV. The pKa's of m- and p-Substituted Aromatic Carbonyl Derivatives1
inferredcites →https://doi.org/10.1021/jo034765bopenalex-snapshot
Total Synthesis of the Depsipeptide FR-901375
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Unexpected Steric Effects of “Remote” Alkyl Groups on the Rate of Conjugate Additions to Alkyl α,β-Ethylenic Sulfones, Sulfoxides, and Esters
inferredcites →https://doi.org/10.1021/jo200163mopenalex-snapshot
Preparation, X-ray Structure, and Reactivity of 2-Iodylpyridines: Recyclable Hypervalent Iodine(V) Reagents
inferredcites →https://doi.org/10.1021/jo801563xopenalex-snapshot
Selective One-Pot Synthesis of Allenyl and Alkynyl Esters from β-Ketoesters
inferredcites →https://doi.org/10.1021/jo970057copenalex-snapshot
Highly Selective Synthesis of Z -Unsaturated Esters by Using New Horner−Emmons Reagents, Ethyl (Diarylphosphono)acetates
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Large-Scale Synthesis of Immunoactivating Natural Product, Pristane, by Continuous Microfluidic Dehydration as the Key Step
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Diisobutylaluminum Hydride Reductions Revitalized: A Fast, Robust, and Selective Continuous Flow System for Aldehyde Synthesis
inferredcites →https://doi.org/10.1021/ol300722eopenalex-snapshot
A Continuous Homologation of Esters: An Efficient Telescoped Reduction–Olefination Sequence
inferredcites →https://doi.org/10.1021/ol4023112openalex-snapshot
Palladium Catalyzed Cyclizations of Oxime Esters with 1,2-Disubstituted Alkenes: Synthesis of Dihydropyrroles
inferredcites →https://doi.org/10.1021/op7002002openalex-snapshot
Dibal-H Reduction of Methyl Butyrate into Butyraldehyde using Microreactors
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Structure and compatibility of a magnesium electrolyte with a sulphur cathode
inferredcites →https://doi.org/10.1039/b906343aopenalex-snapshot
Microchemical systems for continuous-flow synthesis
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Continuous-flow synthesis of vitamin D3
inferredcites →https://doi.org/10.1039/c0ob01169jopenalex-snapshot
Total synthesis of spiruchostatin B aided by an automated synthesizer
inferredcites →https://doi.org/10.1039/c0sc00603copenalex-snapshot
A breakthrough method for the accurate addition of reagents in multi-step segmented flow processing
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Continuous-flow synthesis of activated vitamin D3 and its analogues
inferredcites →https://doi.org/10.1039/c3cc40392kopenalex-snapshot
Reactions of organolithiums with dialkyl oxalates. A flow microreactor approach to synthesis of functionalized α-keto esters
inferredcites →https://doi.org/10.1039/c3cc44709jopenalex-snapshot
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inferredcites →https://doi.org/10.1055/s-0030-1259946openalex-snapshot
Space Integration of Reactions: An Approach to Increase the Capability of Organic Synthesis
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Research and Development of HALAVEN(Eribulin Mesylate)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Direct conversion of esters to aldehydes and ketones via piperazine amide under mild conditions
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ChemInform Abstract: An Efficient Partial Reduction of α,β‐Unsaturated Esters Using DIBAL‐H in Flow.
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Application of Continuous Flow for DIBAL-H Reduction and n-BuLi Mediated Coupling Reaction in the Synthesis of Eribulin Mesylate
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Phosphine-Catalyzed Allylic Fluorides Addition to gem -Difluoroalkenes
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Optimization and sustainability assessment of a continuous flow Ru-catalyzed ester hydrogenation for an important precursor of a β2-adrenergic receptor agonist
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