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An ab Initio Study of the Reactivity of Formylketene. Pseudopericyclic Reactions Revisited

https://doi.org/10.1021/ja00093a028
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The Taumycin A Macrocycle: Asymmetric Total Synthesis and Revision of Relative Stereochemistry
inferred← citeshttps://doi.org/10.1021/ol702628vopenalex-snapshot
A Computational Study of the Formation and Dimerization of Benzothiet-2-one
inferred← citeshttps://doi.org/10.1021/ol8016287openalex-snapshot
The Coupling of Isonitriles and Carboxylic Acids Occurring By Sequential Concerted Rearrangement Mechanisms
inferred← citeshttps://doi.org/10.1021/om300746zopenalex-snapshot
Theoretical Studies on Intramolecular C–H Amination of Biaryl Azides Catalyzed by Four Different Late Transition Metals
inferred← citeshttps://doi.org/10.1023/b:cohc.0000014416.75284.9dopenalex-snapshot
Pericyclic and Heteroelectrocyclic Mechanisms for the Cyclization of 1,3,5-Hexatrien-1-one and Its 6-Aza Analog
inferred← citeshttps://doi.org/10.1023/b:rucb.0000042291.70287.2dopenalex-snapshot
Synthesis and heteroelectrocyclization of unsymmetrically substituted diazomalonamides
inferred← citeshttps://doi.org/10.1039/b003534nopenalex-snapshot
The thioacyl isocyanate–acyl isothiocyanate rearrangement †
inferred← citeshttps://doi.org/10.1039/b202523jopenalex-snapshot
Quinolizine-2,4-diones by reversible dimerisation 2-pyridylketenesElectronic supplementary information (ESI) available: figure of experimental (Ar matrix, 10 K) IR spectrum of 10b and calculated (B3LYP/6-31G*) IR spectra of s-cis- and s-trans-10b, and tables of Cartesian coordinates and calculated…
inferred← citeshttps://doi.org/10.1039/b309549eopenalex-snapshot
Ketene–acetylene [2 + 2] cycloadditions: cyclobutenone and/or oxete formation?
inferred← citeshttps://doi.org/10.1039/b312559aopenalex-snapshot
Selective esterifications of alcohols and phenols through carbodiimide couplingsElectronic supplementary information (ESI) available: the characterization of new compounds and literature references for known compounds. See http://www.rsc.org/suppdata/ob/b3/b312559a/
inferred← citeshttps://doi.org/10.1039/b412530dopenalex-snapshot
Imidoylketene dimerization and rearrangement
inferred← citeshttps://doi.org/10.1039/b504260gopenalex-snapshot
Imidoylketene-α-oxoketenimine and α-oxoketene–α-oxoketene rearrangements. 1,3-Shifts of substituted phenyl groups
inferred← citeshttps://doi.org/10.1039/b515917bopenalex-snapshot
Oxoketene–oxoketene, imidoylketene–imidoylketene and oxoketenimine–imidoylketene rearrangements. 1,3-Shifts of phenyl groups
inferred← citeshttps://doi.org/10.1039/b705457mopenalex-snapshot
Reactions in the conjugated ‘ene–ene–yne’ manifold: five-membered ring fragmentation and ring formation via coarctate/pseudocoarctate mechanisms
inferred← citeshttps://doi.org/10.1039/b718080bopenalex-snapshot
Microwave generation and trapping of acetylketene
inferred← citeshttps://doi.org/10.1039/c39950002547openalex-snapshot
Kinetic and theoretical studies of the hydration of carbon suboxide
inferred← citeshttps://doi.org/10.1039/c3np20110dopenalex-snapshot
Advances in the total synthesis of biologically important callipeltosides: a review
inferred← citeshttps://doi.org/10.1039/cc9960000775openalex-snapshot
Thermal cycloreversion of 4H-1,3-dioxine-4-thiones to acyl thioketenes:a general synthesis of β-keto thioic O-acid derivatives
inferred← citeshttps://doi.org/10.1039/d2cc04805aopenalex-snapshot
Recent advances in 8π electrocyclization reactions
inferred← citeshttps://doi.org/10.1039/d2sc04092aopenalex-snapshot
Phosphine-catalyzed activation of cyclopropenones: a versatile C 3 synthon for (3+2) annulations with unsaturated electrophiles
inferred← citeshttps://doi.org/10.1039/d4qo00613eopenalex-snapshot
Green synthesis of glutaramides, piperidino[1,2- a ]benzimidazol-1-ones and N -cyclopentenyl benzimidazolones enabled by microwave assisted domino reactions of cyclic 2-diazo-1,3-diketones with aniline derivatives
inferred← citeshttps://doi.org/10.1071/ch08523openalex-snapshot
Interconversion of Nitrenes, Carbenes, and Nitrile Ylides by Ring Expansion, Ring Opening, Ring Contraction, and Ring Closure: 3-Quinolylnitrene, 2-Quinoxalylcarbene, and 3-Quinolylcarbene
inferred← citeshttps://doi.org/10.1246/bcsj.77.1671openalex-snapshot
Natural Bond Orbital Analysis of Pericyclic and Pseudopericyclic 1,5-Electrocyclizations of Conjugated Nitrileimines
inferred← citeshttps://doi.org/10.1246/cl.2006.1242openalex-snapshot
Substituent Effects on Two Orthogonal π-Systems in Pseudopericyclic Ring-opening Reactions of 5-Alkoxy-2-aminooxazoles
inferred← citeshttps://doi.org/10.14233/ajchem.2019.21646openalex-snapshot
Theoretical Study of Sigmatropic Rearrangement of Cycloprop-2-en-1-ol and its Fluorine Derivatives: Pericyclic or Pseudopericyclic Character from NICS and LLPE
inferred← citeshttps://doi.org/10.2174/138527210793563279openalex-snapshot
Cumulene Rearrangements: Ketene-Ketene, Isocyanate-Isocyanate, Thioketene-Ketene, Imidoylketene-Ketenimine, and Ketene-Allene Rearrangements
inferred← citeshttps://doi.org/10.3987/com-02-9504openalex-snapshot
Reactions of a-Oxo Ketenes with Amides: Experimental Data and Semiempirical AM1 Molecular Orbital Calculations
inferred← citeshttps://doi.org/10.3987/com-05-10477openalex-snapshot
Natural Bond Orbital Analysis of Pericyclic and Pseudopericyclic 1,5-Electrocyclizations of Conjugated Azides
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