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A highly stereoselective ether directed palladium catalysed aza-Claisen rearrangement
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.198405791openalex-snapshot
Mercury( II )‐ and Palladium( II )‐Catalyzed [3,3]‐Sigmatropic Rearrangements [New Synthetic Methods (46)]
inferredcites →https://doi.org/10.1016/s0040-4020(01)88337-xopenalex-snapshot
Diastereoselectivity of the thio-Claisen rearrangement of acyclic precursors bearing a chiral centre adjacent to carbon 6
inferredcites →https://doi.org/10.1016/s0040-4039(00)74248-1openalex-snapshot
Synthesis of (E)β,γ-unsaturated α-aminoacids by rearrangement of allyltrichloroacetimidates
inferredcites →https://doi.org/10.1021/ar50151a005openalex-snapshot
Allylic and propargylic imidic esters in organic synthesis
inferredcites →https://doi.org/10.1021/ja00293a041openalex-snapshot
Homogeneous catalysis. Transition-metal-catalyzed Claisen rearrangements
inferredcites →https://doi.org/10.1021/ja037086ropenalex-snapshot
Catalytic Asymmetric Rearrangement of Allylic Trichloroacetimidates. A Practical Method for Preparing Allylic Amines and Congeners of High Enantiomeric Purity
inferredcites →https://doi.org/10.1021/ja970402fopenalex-snapshot
Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones
inferredcites →https://doi.org/10.1021/jo00055a047openalex-snapshot
A study of the 3,3-sigmatropic rearrangement of chiral trichloroacetamidic esters
inferredcites →https://doi.org/10.1021/jo962090popenalex-snapshot
First Enantioselective Catalyst for the Rearrangement of Allylic Imidates to Allylic Amides
inferredcites →https://doi.org/10.1021/ol0271786openalex-snapshot
Catalytic Asymmetric Rearrangement of Allylic N-Aryl Trifluoroacetimidates. A Useful Method for Transforming Prochiral Allylic Alcohols to Chiral Allylic Amines
inferredcites →https://doi.org/10.1039/b401076kopenalex-snapshot
The first enantioselective synthesis of the amino acid, (2S,3S,4R)-γ-hydroxyisoleucine using a palladium( ii ) catalysed 3,3-sigmatropic rearrangement
inferredcites →https://doi.org/10.1055/s-1993-25930openalex-snapshot
Diastereoselective Synthesis of 1,2-Diamines by Palladium Catalyzed Aza-Claisen Rearrangement
inferredcites →https://doi.org/10.15227/orgsyn.058.0004openalex-snapshot
ALLYLICALLY TRANSPOSED AMINES FROM ALLYLIC ALCOHOLS: 3,7-DIMETHYL-1,6-OCTADIEN-3-AMINE
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4622797openalex-extracted
Sialyl Lewis x Glycomimetics Bearing an Extended Anionic Chain Targeting E- and P- Selectin Binding Sites
inferred← citeshttps://doi.org/10.1002/9780470638859.conrr029openalex-snapshot
Aza‐Claisen Rearrangement
inferred← citeshttps://doi.org/10.1002/9781118662083.cot09-007openalex-snapshot
Formation of Nitriles, Carboxylic Acids, and Derivatives by Rearrangements
inferred← citeshttps://doi.org/10.1002/chem.201102716openalex-snapshot
Stereoselective Palladium‐Catalyzed Functionalization of Homoallylic Alcohols: A Convenient Synthesis of Di‐ and Trisubstituted Isoxazolidines and β‐Amino‐δ‐Hydroxy Esters
inferred← citeshttps://doi.org/10.1002/chin.200531044openalex-snapshot
A Highly Stereoselective Ether Directed Palladium Catalyzed Aza‐Claisen Rearrangement.
inferred← citeshttps://doi.org/10.1002/ejoc.200700782openalex-snapshot
A Temporary Stereocentre Approach for the Stereodivergent Synthesis of Either Enantiomer of α‐Methyloctanal
inferred← citeshttps://doi.org/10.1016/j.bmc.2023.117553openalex-snapshot
Sialyl LewisX glycomimetics bearing an extended anionic chain targeting E- and P- selectin binding sites
inferred← citeshttps://doi.org/10.1016/j.ccr.2007.03.011openalex-snapshot
Transition metals in organic synthesis: Highlights for the year 2005
inferred← citeshttps://doi.org/10.1016/j.tet.2006.12.067openalex-snapshot
Ether-directed palladium(II)-catalysed aza-Claisen rearrangements: studies on the origin of the directing effect
inferred← citeshttps://doi.org/10.1016/j.tet.2007.10.079openalex-snapshot
Catalysis of the Claisen rearrangement
inferred← citeshttps://doi.org/10.1016/j.tet.2008.03.099openalex-snapshot
Ether-directed diastereoselectivity in catalysed Overman rearrangement: comparative studies of metal catalysts
inferred← citeshttps://doi.org/10.1016/j.tet.2008.07.062openalex-snapshot
Studies on the aza-Claisen rearrangement of 4,5-dihydroxylated allylic trichloroacetimidates: the stereoselective synthesis of (2R,3S)- and (2S,3S)-2-amino-3,4-dihydroxybutyric acids
inferred← citeshttps://doi.org/10.1016/j.tet.2011.03.011openalex-snapshot
Diversity oriented synthesis: substitution at C5 in unreactive pyrimidines by Claisen rearrangement and reactivity in nucleophilic substitution at C2 and C4 in pteridines and pyrido[2,3-d]pyrimidines
inferred← citeshttps://doi.org/10.1016/j.tet.2019.04.067openalex-snapshot
Synergistic substrate and catalyst effects in the addition of trimethylsilyl cyanide to imines derived from lactic acid
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.11.010openalex-snapshot
A concise enantioselective synthesis of (2S,3S)-3-hydroxypipecolic acid via proline catalyzed α-aminooxylation of aldehydes and Pd-catalyzed ether directed aza-Claisen rearrangements
inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.03.011openalex-snapshot
First enantioselective synthesis of (2S,3S)-3-hydroxy-l-arginine via proline catalyzed α-aminooxylation of aldehyde and Pd-catalyzed ether-directed aza-Claisen rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.03.161openalex-snapshot
A stereoselective synthesis of (2R,3S)-2-amino-3,4-dihydroxybutyric acid using an ether directed aza-Claisen rearrangement
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.02.032openalex-snapshot
Tandem aza-Claisen rearrangement and ring-closing metathesis reactions: the stereoselective synthesis of functionalised carbocyclic amides
inferred← citeshttps://doi.org/10.1021/ja403823nopenalex-snapshot
Total Synthesis of (±)-Gelsemoxonine
inferred← citeshttps://doi.org/10.1021/jacs.5b02574openalex-snapshot
Total Synthesis of Gelsemoxonine through a Spirocyclopropane Isoxazolidine Ring Contraction
inferred← citeshttps://doi.org/10.1021/jo401211jopenalex-snapshot
Preparation of anti-Vicinal Amino Alcohols: Asymmetric Synthesis of d -erythro-Sphinganine, (+)-Spisulosine, and d -ribo-Phytosphingosine
inferred← citeshttps://doi.org/10.1021/jo502111copenalex-snapshot
Regio- and Stereocontrol in the Reactions of α-Halo-β,γ-enoates and α-O-Phosphono-β,γ-enenitriles with Organocuprates
inferred← citeshttps://doi.org/10.1021/ol070424zopenalex-snapshot
Ether-Directed, Stereoselective Aza-Claisen Rearrangements: Synthesis of the Piperidine Alkaloid, α-Conhydrine
inferred← citeshttps://doi.org/10.1021/ol702299copenalex-snapshot
A Tandem Aza-Claisen Rearrangement and Ring Closing Metathesis Reaction for the Synthesis of Cyclic Allylic Trichloroacetamides
inferred← citeshttps://doi.org/10.1039/b510808jopenalex-snapshot
Stereoselective β-hydroxy-α-amino acid synthesis via an ether-directed, palladium-catalysed aza-Claisen rearrangement
inferred← citeshttps://doi.org/10.1039/b607014kopenalex-snapshot
Scope and limitations of ether-directed, metal-catalysed aza-Claisen rearrangements; improved stereoselectivity using non-coordinating solvents
inferred← citeshttps://doi.org/10.1039/b613271eopenalex-snapshot
Stereocontrol of palladium(ii)-catalysed aza-Claisen rearrangements using a combination of 1,3-allylic strain and a solvent mediated directing effect
inferred← citeshttps://doi.org/10.1039/c0ob00219dopenalex-snapshot
Stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin
inferred← citeshttps://doi.org/10.1039/c1ob06060kopenalex-snapshot
Total synthesis of clavaminol A, C and H
inferred← citeshttps://doi.org/10.1039/c2ob25334hopenalex-snapshot
Stereoselective synthesis of functionalised carbocyclic amides: construction of the syn-(4aS,10bS)-phenanthridone skeleton
inferred← citeshttps://doi.org/10.1039/c6cc06047aopenalex-snapshot
Enantioselective synthesis of β-substituted chiral allylic amines via Rh-catalyzed asymmetric hydrogenation
inferred← citeshttps://doi.org/10.1039/c6ob02625gopenalex-snapshot
Recent advances in the Overman rearrangement: synthesis of natural products and valuable compounds
inferred← citeshttps://doi.org/10.1039/d2ob00166gopenalex-snapshot
Synthetic studies towards naturally occurring γ-( Z )/( E )-alkylidenebutenolides through bimetallic cascade cyclization and an adventitious photoisomerization method
inferred← citeshttps://doi.org/10.70675/cd98cac0z59dez4ad2zaf24z6cf96f6febd0openalex-snapshot
Synthèse d’inhibiteurs spécifiques de la Neuraminidase-1 humaine
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