Results 171 to 180 of about 3,654 (228)
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Organic Letters, 2023
P(NMe2)3-mediated substrate-controlled annulations of azoalkenes with α-dicarbonyl compounds are reported, where the azoalkenes serve as either four or five-atom synthons chemoselectively.
Yunfeng Du+4 more
semanticscholar +1 more source
P(NMe2)3-mediated substrate-controlled annulations of azoalkenes with α-dicarbonyl compounds are reported, where the azoalkenes serve as either four or five-atom synthons chemoselectively.
Yunfeng Du+4 more
semanticscholar +1 more source
Expeditious entry into carbocyclic and heterocyclic spirooxindoles
Organic & Biomolecular Chemistry, 2022Recent advances in the chemistry of base-, metal-, nano-metal and organo-catalyst mediated achiral and chiral versions of the structurally diverse and pharmaceutically relevant spirooxindoles are gently reviewed.
Madhu Ganesh, Shammy Suraj
openaire +2 more sources
Organic Letters, 2023
A novel method for the enantioselective synthesis of spiro N,N-heterocyclic oxindoles has been developed, employing asymmetric [4 + 2]-cycloadditions of 2-aminophenyl enones with isatin-derived ketimines.
Ji Won Han, Yoseop Kim, Sung-Gon Kim
semanticscholar +1 more source
A novel method for the enantioselective synthesis of spiro N,N-heterocyclic oxindoles has been developed, employing asymmetric [4 + 2]-cycloadditions of 2-aminophenyl enones with isatin-derived ketimines.
Ji Won Han, Yoseop Kim, Sung-Gon Kim
semanticscholar +1 more source
Organocatalytic Asymmetric Synthesis of Spirooxindole Embedded Oxazolidines [PDF]
The first organocatalytic asymmetric synthesis of spirooxindole embedded oxazolidines has been developed via a domino reaction involving hemiaminal formation, followed by an unprecedented aza-Michael reaction between isatin derived N-Boc ketimines and γ-hydroxy enones.
Chandrakanta Parida+3 more
openaire +2 more sources
Advanced Synthesis & Catalysis, 2023
We report here a practical protocol for the asymmetric synthesis of AAs with a CF3‐containing 3,2’‐pyrrolidinyl spirooxindole skeleton with three defined carbon stereocenters via a sequential Michael/Mannich [3+2]‐cycloaddition reaction.
Z. Gugkaeva+5 more
semanticscholar +1 more source
We report here a practical protocol for the asymmetric synthesis of AAs with a CF3‐containing 3,2’‐pyrrolidinyl spirooxindole skeleton with three defined carbon stereocenters via a sequential Michael/Mannich [3+2]‐cycloaddition reaction.
Z. Gugkaeva+5 more
semanticscholar +1 more source
Synthetic Communications, 2023
Synthesis of spirooxindole derivatives was achieved by combining Knoevenagel condensation and Michael addition between isatin, malononitrile, and dimedone or cyclohexan-1,3-dione in presence of ammonium acetate by simple stirring in ethanol at room ...
Barkha K. Raheja, D. Dalal
semanticscholar +1 more source
Synthesis of spirooxindole derivatives was achieved by combining Knoevenagel condensation and Michael addition between isatin, malononitrile, and dimedone or cyclohexan-1,3-dione in presence of ammonium acetate by simple stirring in ethanol at room ...
Barkha K. Raheja, D. Dalal
semanticscholar +1 more source
Synthesis, 2023
A higly functionalized spirooxindole pyrrolizidine/pyrrolothiazole derivatives has been synthesised by the three-component 1,3-dipolar cycloaddition reaction of benzothiazolyl amides with isatin-based azomethine ylides.
Narayanasamy Nivetha+4 more
semanticscholar +1 more source
A higly functionalized spirooxindole pyrrolizidine/pyrrolothiazole derivatives has been synthesised by the three-component 1,3-dipolar cycloaddition reaction of benzothiazolyl amides with isatin-based azomethine ylides.
Narayanasamy Nivetha+4 more
semanticscholar +1 more source
ChemInform Abstract: A New Route to Spirooxindoles.
ChemInform, 2000AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Tim C. T. Ho+3 more
openaire +4 more sources
ChemInform Abstract: Strategies for the Enantioselective Synthesis of Spirooxindoles.
ChemInform, 2012AbstractReview: 85 refs.
Nicolas R. Ball-Jones+2 more
openaire +4 more sources
Journal of Organic Chemistry, 2022
The additive-free [3 + 2] annulation from isatins, amino acids with 2-styrylbenzoxazoles, was described, providing a series of functional and structurally complex 3,3'-pyrrolidinyl-spirooxindole derivatives containing four contiguous and two quaternary ...
Kaikai Wang+6 more
semanticscholar +1 more source
The additive-free [3 + 2] annulation from isatins, amino acids with 2-styrylbenzoxazoles, was described, providing a series of functional and structurally complex 3,3'-pyrrolidinyl-spirooxindole derivatives containing four contiguous and two quaternary ...
Kaikai Wang+6 more
semanticscholar +1 more source