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Structure–Reactivity Relationships of Zwitterionic 1,3-Diaza-Claisen Rearrangements
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Säureamid‐Reaktionen, XXVII. Umsetzungen mit Säureamid‐Phosphoroxychlorid‐Addukten und Amidchloriden
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Synthesis of highly substituted ureas and thioureas through 1,3-diaza-Claisen rearrangements
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Nachweis innermolekularer beweglichkeit durch NMR-spektroskopie—XV
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A facile synthesis of cyanoguanidines from thioureas
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Effect of conformational change on reactivity in organic chemistry. Evaluations, applications, and extensions of Curtin-Hammett Winstein-Holness kinetics
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Design of a New Cascade Reaction for the Construction of Complex Acyclic Architecture: The Tandem Acyl-Claisen Rearrangement
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Diastereoselective Zwitterionic Aza-Claisen Rearrangement: The Synthesis of Bicyclic Tetrahydrofurans and a Total Synthesis of (+)-Dihydrocanadensolide
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Facile 1,3-diaza-Claisen Rearrangements of Tertiary Allylic Amines Bearing an Electron-Deficient Alkene
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Selective Synthesis of Eight-Membered Cyclic Ureas by the [6 + 2] Cycloaddition Reaction of 2-Vinylazetidines and Electron-Deficient Isocyanates
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A Formal Pd0-Catalyzed 1,3-Diaza-Claisen Rearrangement
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Rolf Huisgen's Classic Studies of Cyclic Triene Diels–Alder Reactions Elaborated by Modern Computational Analysis
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Rolf Huisgen's Classic Studies of Cyclic Triene Diels–Alder Reactions Elaborated by Modern Computational Analysis
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ChemInform Abstract: Structure—Reactivity Relationships of Zwitterionic 1,3‐Diaza‐Claisen Rearrangements.
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Synthesis of Guanidines and Some of Their Biological Applications
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Novel E-F ring derivatives of aconitine scaffold as potent Hsp90 inhibitors for the treatment of colorectal cancer
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Cationic 1-thia-3-aza-Claisen rearrangement entry to cyclic S-allylic isothioureas
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.04.064openalex-snapshot
Optimization of methods for the generation of carbodiimides for zwitterionic 1,3-diaza-Claisen rearrangements
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Rearrangement of 2-azanorbornenes to tetrahydrocyclopenta[c]pyridines under the action of activated alkynes – A short pathway for construction of the altemicidin core
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A formal Pd0-catalyzed 1,3-diaza-Claisen rearrangement
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α-Imino Esters in Organic Synthesis: Recent Advances
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Recent Advances in the Synthesis of Hydantoins: The State of the Art of a Valuable Scaffold
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Asymmetric Aza-Claisen Rearrangement between Enantioenriched α-Chiral Allylamines and Allenones
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00667openalex-snapshot
Broadening the Scope of the Zwitterionic 1,3-Diaza-Claisen Rearrangement through a Tethering Strategy
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02524openalex-snapshot
1,3-Diaza-Claisen Rearrangements of Vinyl Pyrrolidines Tethered to In Situ Generated Carbodiimides Afford Ring-Expanded [9,5]- and [9,6]-Bicyclic Guanidines
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02655openalex-snapshot
Modular Synthesis of Enantioenriched α-Chiral Homoallylic Amidines Enabled by Relay Ir/Cu Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01746openalex-snapshot
Intramolecular Formation of Zwitterionic Intermediates in 1,3-Diaza-Claisen Rearrangements
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Acyl Azides: Versatile Compounds in the Synthesis of Various Heterocycles
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Crystal structures of sulfonamide protected bicyclic guanidines: (S)-8-{[(tert-butyldimethylsilyl)oxy]methyl}-1-[(2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran-5-yl)sulfonyl]-1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidin-1-ium trifluoromethanesulfonate and…
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Enantioselective synthesis of α-amino esters through Petasis borono-Mannich multicomponent reaction of potassium trifluoroborate salts
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