[3+2] Dipolar Cycloaddition of a Stabilized Azomethine Ylide and an Electron-Deficient Dipolarophile: Revision of Regioselectivity. [PDF]
J Org Chem, 2023 The regioselectivity of a [3+2] dipolar cycloaddition reaction of a stabilized azomethine ylide with an electron-deficient dipolarophile was found to be counter to a report published in this ...
Wu KJY, Benedetto AE, Myers AG.
europepmc +3 more sources
Correction: Covalent organic functionalization of graphene nanosheets and reduced graphene oxide via 1,3-dipolar cycloaddition of azomethine ylide. [PDF]
Nanoscale Adv, 2021 Correction for ‘Covalent organic functionalization of graphene nanosheets and reduced graphene oxide via 1,3-dipolar cycloaddition of azomethine ylide’ by Luca Basta et al., Nanoscale Adv., 2021, DOI: 10.1039 ...
Basta L +9 more
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Oxazolium salt/azomethine ylide approach to aziridinomitosenes.
, 2002 An enantioselective synthesis of aziridinomitosenes and analogs thereof was investigated using an intramolecular oxazolium salt/azomethine ylide cycloaddition sequence to construct the indoloquinone tetracyclic core.
Warner, Don Lewis
core +6 more sources
Synthesis of diversely substituted bis-pyrrolizidino/ thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids via sequential azomethine ylide cycloaddition. [PDF]
RSC Adv, 2018 Curcumin has been transformed to several diversely substituted bis-pyrrolizidino/thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids via a sequential azomethine ylide cycloaddition reaction.
Singh M +8 more
europepmc +2 more sources
Approach to the Homoerythrina Alkaloids Using a Tandem N-Alkylation/Azomethine Ylide Cycloaddition
, 2016 Synthetic efforts toward the homoerythrina alkaloids 1−3 are described. Two separate model systems guided the pivotal [3 + 2] azomethine ylide cycloaddition cascade to form the A−C rings of these alkaloids.
Jeff W. Kampf (1537393) +4 more
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iScience, 2019 Summary: Development of a general catalytic and highly efficient method utilizing readily available precursors for the regio- and stereoselective construction of bioactive natural-product-inspired spiro architectures remains a formidable challenge in ...
Chong Shen +5 more
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Crystals, 2023 A new ethylene derivative was synthesized as a precursor for the [3+2] cycloaddition (32CA) reaction to access a novel spirooxindole embodied with benzimidazole with a pyridine spacer.
Saeed Alshahrani +4 more
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General Approach toward Aspidospermatan-Type Alkaloids Using One-Pot Vilsmeier–Haack Cyclization and Azomethine Ylide Cycloaddition [PDF]
, 2017 : The development of a new one-pot reaction sequence afforded the tricyclic core of several aspidospermatan-type alkaloids from a linear, densely functionalized substrate.
Guillaume Bélanger +3 more
core +1 more source
Molecules, 2020 Our synthetic approach for the assembly of structurally complex spirooxindole heterocyclic hybrids was based on an ionic liquid, [bmim]Br mediated one-pot three-component cascade reaction strategy involving 1,3-dipolar cycloaddition reaction of N-1-(2 ...
Raju Suresh Kumar +4 more
doaj +1 more source
Cationic Pyrrolidine/Pyrroline-Substituted Porphyrins as Efficient Photosensitizers against E. coli
Molecules, 2021 New porphyrin–pyrrolidine/pyrroline conjugates were prepared by revisiting 1,3-dipolar cycloaddition reactions between a porphyrinic azomethine ylide and a series of dipolarophiles.
Bruno M. F. Ladeira +7 more
doaj +1 more source