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Hydrogen-Bond-Promoted Hetero-Diels−Alder Reactions of Unactivated Ketones
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Hydrogen Bonding by C—H Groups
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Reactions of ketene acetals 15. Regiospecific syntheses of erythrolaccin and “7-hydroxyerythrolaccin”.
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Highly Enantioselective Diels−Alder Reactions of 1-Amino-3-siloxy-dienes Catalyzed by Cr(III)-Salen Complexes
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Donor and acceptor strengths in C–H···O hydrogen bonds quantified from crystallographic data of small solvent molecules
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1021/jp054048gopenalex-snapshot
Toward an Understanding of the Catalytic Role of Hydrogen-Bond Donor Solvents in the Hetero-Diels−Alder Reaction between Acetone and Butadiene Derivative
inferred← citeshttps://doi.org/10.1021/ol0347444openalex-snapshot
Acid-Promoted Olefination of Ketones by an Iron(III) Porphyrin Complex
inferred← citeshttps://doi.org/10.1021/ol0495624openalex-snapshot
Stereoselective Ketal-Tethered Intramolecular Diels−Alder Cycloadditions. An Approach to the 2-Oxadecalin Spiroketal Core of Antifungal Agent Fusidilactone C
inferred← citeshttps://doi.org/10.1021/ol0629925openalex-snapshot
Hydrogen Bonding Catalysis Operates by Charge Stabilization in Highly Polar Diels−Alder Reactions
inferred← citeshttps://doi.org/10.1021/ol1007873openalex-snapshot
Asymmetric Synthesis of Spiro-3,4-dihydropyrans via a Domino Organocatalytic Sequence
inferred← citeshttps://doi.org/10.1021/ol101705jopenalex-snapshot
A Biomimetic Total Synthesis of (+)-Ainsliadimer A
inferred← citeshttps://doi.org/10.1021/ol400894jopenalex-snapshot
Efficient Enantioselective Synthesis of Dihydropyrans Using a ChiralN,N′-Dioxide as Organocatalyst
inferred← citeshttps://doi.org/10.1021/ol400904yopenalex-snapshot
A Redox Economical Synthesis of Bioactive 6,12-Guaianolides
inferred← citeshttps://doi.org/10.1021/ol802134aopenalex-snapshot
Cu(I)-Catalyzed Hetero-Diels−Alder Reaction between Danishefsky-Type Siloxy Dienes and Ketones
inferred← citeshttps://doi.org/10.1038/424146aopenalex-snapshot
Single enantiomers from a chiral-alcohol catalyst
inferred← citeshttps://doi.org/10.1038/ncomms7913openalex-snapshot
Synthesis of tetrasubstituted 1-silyloxy-3-aminobutadienes and chemistry beyond Diels–Alder reactions
inferred← citeshttps://doi.org/10.1039/9781782622482-00010openalex-snapshot
Synthesis and Applications of Preformed Dienamines
inferred← citeshttps://doi.org/10.1039/9781788016490-00066openalex-snapshot
Catalysis by Networks of Cooperative Hydrogen Bonds
inferred← citeshttps://doi.org/10.1039/b713104fopenalex-snapshot
A deep cavitand catalyzes the Diels–Alder reaction of bound maleimides
inferred← citeshttps://doi.org/10.1039/b818655copenalex-snapshot
Synergistic activation of the Diels–Alder reaction by an organic catalyst and substituents: a computational study
inferred← citeshttps://doi.org/10.1039/c0ob00174kopenalex-snapshot
A facile method for the synthesis of oxindole based quaternary α-aminonitriles via the Strecker reaction
inferred← citeshttps://doi.org/10.1039/c2cp41719gopenalex-snapshot
Microsolvated transition state models for improved insight into chemical properties and reaction mechanisms
inferred← citeshttps://doi.org/10.1039/c2gc36619copenalex-snapshot
Cyclometalated iridium complexes for transfer hydrogenation of carbonyl groups in water
inferred← citeshttps://doi.org/10.1039/c3cs60025dopenalex-snapshot
Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis
inferred← citeshttps://doi.org/10.1039/c4cc03896gopenalex-snapshot
A catalytic asymmetric hetero-Diels–Alder reaction of olefinic azlactones and isatins: facile access to chiral spirooxindole dihydropyranones
inferred← citeshttps://doi.org/10.1039/c4nj02361gopenalex-snapshot
Organocatalytic oxa-Diels–Alder reaction of α,β-unsaturated ketones under non-classical conditions
inferred← citeshttps://doi.org/10.1039/c5ob01125fopenalex-snapshot
An efficient catalyst-free Mukaiyama-aldol reaction of fluorinated enol silyl ethers with tryptanthrin
inferred← citeshttps://doi.org/10.1039/c5ra17488kopenalex-snapshot
Recent applications of the hetero Diels–Alder reaction in the total synthesis of natural products
inferred← citeshttps://doi.org/10.1039/c6qo00018eopenalex-snapshot
Direct construction of chiral quaternary dihydropyranones through highly enantioselective organocatalytic hetero-Diels–Alder reactions of olefinic azlactones
inferred← citeshttps://doi.org/10.1039/c7ob02424jopenalex-snapshot
Organocatalytic umpolung annulative dimerization of ynones for the synthesis of 5-alkylidene-2-cyclopentenones
inferred← citeshttps://doi.org/10.1039/c7ob03002aopenalex-snapshot
Catalytic synthesis of 3-aminooxindoles via addition to isatin imine: an update
inferred← citeshttps://doi.org/10.1039/c9sc05196aopenalex-snapshot
Development of copper-catalyzed enantioselective decarboxylative aldolization for the preparation of perfluorinated 1,3,5-triols featuring supramolecular recognition properties
inferred← citeshttps://doi.org/10.1039/d0cc00702aopenalex-snapshot
( Z )-Selective anti-Markovnikov or Markovnikov thiol–yne-click reactions of an internal alkyne by amide hydrogen bond control
inferred← citeshttps://doi.org/10.1039/d0ob02149kopenalex-snapshot
Catalyst-free and additive-free reactions enabling C–C bond formation: a journey towards a sustainable future
inferred← citeshttps://doi.org/10.1039/d1nj01373dopenalex-snapshot
Theoretical investigation of the effect of hydrogen bonding on the stereoselectivity of the Diels–Alder reaction
inferred← citeshttps://doi.org/10.1039/d1ob01415copenalex-snapshot
The catalytic effects of a thiazolium salt in the oxa-Diels–Alder reaction between benzaldehyde and Danishefsky's diene: a molecular electron density theory study
inferred← citeshttps://doi.org/10.1039/d2qo01730jopenalex-snapshot
Hydrogen Bonding-directed Sequential 1,6/1,4-Addition of Heteroatom Nucleophiles onto Electron-deficient 1,3-Diynes
inferred← citeshttps://doi.org/10.1055/sos-sd-237-00049openalex-snapshot
4 Organocatalytic Dynamic Kinetic Asymmetric Transformations
inferred← citeshttps://doi.org/10.1073/pnas.0307025101openalex-snapshot
Asymmetric hetero-Diels–Alder reaction catalyzed by dirhodium(II) carboxamidates
inferred← citeshttps://doi.org/10.1073/pnas.0307176101openalex-snapshot
Enantioselective direct aldol reactions catalyzed by l -prolinamide derivatives
inferred← citeshttps://doi.org/10.1073/pnas.0308545101openalex-snapshot
Enantioselective Diels–Alder reactions catalyzed by hydrogen bonding
inferred← citeshttps://doi.org/10.1080/00268976.2013.846485openalex-snapshot
On the importance of hydrogen bonding in the promotion of Diels–Alder reactions of unactivated aldehydes: a computational study
inferred← citeshttps://doi.org/10.1080/08927022.2014.904514openalex-snapshot
Quantum chemical topological analysis of hydrogen bonding in HX…HX and CH3X…HX dimers (X = Br, Cl, F)
inferred← citeshttps://doi.org/10.1134/s1070428011010015openalex-snapshot
Aliphatic aldehydes in the synthesis of carbo- and heterocycles: Part II. Synthesis of six- and seven-membered rings, bicyclic compounds, and macrocycles
inferred← citeshttps://doi.org/10.1246/cl.130672openalex-snapshot
Iron Corrole-catalyzed [4 + 2] Cycloaddition of Dienes and Aldehydes
inferred← citeshttps://doi.org/10.1248/cpb.58.593openalex-snapshot
Development of Chiral Thiourea Catalysts and Its Application to Asymmetric Catalytic Reactions
inferred← citeshttps://doi.org/10.3390/ijms24054938openalex-snapshot
Unravelling the Mechanism and Governing Factors in Lewis Acid and Non-Covalent Diels–Alder Catalysis: Different Perspectives
inferred← citeshttps://doi.org/10.3987/com-06-s(o)52openalex-snapshot
Hetero Diels-Alder Type Reactions Between Danishefsky’s Dienes in the Presence of Lewis Base Catalysts. An Efficient Method for the Synthesis of Substituted 2,3-Dihydropyran-4-ones
inferred← citeshttps://doi.org/10.3987/com-10-s(e)93openalex-snapshot
A Cyclic Acetal Tethered Intramolecular Diels-Alder Cycloaddition. Studies Directed toward a Total Synthesis of (±)-Fusidilactone C
inferred← citeshttps://doi.org/10.3998/ark.5550190.p009.252openalex-snapshot
Direct organocatalytic Wittig/Hetero-Diels-Alder reactions in one-pot: synthesis of highly-substituted tetrahydropyranones
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.77.553openalex-snapshot
Asymmetric Hetero-Diels-Alder Reactions Catalyzed by Chiral Dirhodium(II) Complexes
inferred← citeshttps://doi.org/10.5772/24349openalex-snapshot
1,2,3-Triazolium Salts as a Versatile New Class of Ionic Liquids
inferred← citeshttps://doi.org/10.70675/4539e733z2d8cz4e4az8668ze79ac26cee9copenalex-snapshot
Biomimetic asymmetric catalysis with bioinspired helical foldamers
inferred← citeshttps://doi.org/10.70675/b68bd9f0zdb17z4375zb7ceze178ace3c7abopenalex-snapshot
Design, synthesis and applications of new chiral bifunctional iminophosphorane - thiourea organocatalysts. Organophotocatalytic addition of unactivated alkenes with silicon enolate
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