Articles with "cycloaddition azomethine" as a keyword



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CuII-catalysed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with a chiral ferrocene-derived P,N-ligand

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Published in 2017 at "Tetrahedron Letters"

DOI: 10.1016/j.tetlet.2017.05.044

Abstract: A ferrocene-derived P,N-heterodonor ligand was effectively used in a Cu(OAc)2·H2O-catalysed asymmetric 1,3-dipolar cycloaddition of azomethine ylides with maleate derivatives, affording cycloadducts with high yields (up to 96%), diastereoselectivities (>99 dr), and enantioselectivities (up to 99%… read more here.

Keywords: asymmetric dipolar; azomethine ylides; catalysed asymmetric; ferrocene derived ... See more keywords
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Asymmetric Formal [3 + 2]-Cycloaddition of Azomethine Imines with Azlactones To Synthesize Bicyclic Pyrazolidinones.

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Published in 2017 at "Organic letters"

DOI: 10.1021/acs.orglett.7b02772

Abstract: An efficient enantioselective formal [3 + 2]-cycloaddition of azomethine imines with azlactones has been realized by using a chiral bifunctional bisguanidinium hemisalt as the catalyst. Optically active bicyclic pyrazolidinone compounds were generated under mild reaction… read more here.

Keywords: formal cycloaddition; imines azlactones; azomethine imines; cycloaddition azomethine ... See more keywords
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DABCO-mediated [3+3] cycloaddition of azomethine imines with in situ generated nitrile oxides from hydroximoyl chlorides.

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Published in 2019 at "Chemical communications"

DOI: 10.1039/c9cc05367k

Abstract: A novel cross 1,3-dipolar cycloaddition between azomethine imines with in situ generated nitrile oxides has been developed. This is the first example of employing a reaction partner containing two heteroatoms in the [3+3] cycloaddition involving… read more here.

Keywords: nitrile oxides; azomethine imines; cycloaddition azomethine; imines situ ... See more keywords

Regio- and stereoselective synthesis of spiropyrrolidine-oxindole and bis-spiropyrrolizidine-oxindole grafted macrocycles through [3 + 2] cycloaddition of azomethine ylides

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Published in 2020 at "RSC Advances"

DOI: 10.1039/c9ra10463a

Abstract: A convenient and efficient method for the regioselective macrocyclization of triazole bridged spiropyrrolidine-oxindole, and bis-spiropyrrolizidine-oxindole derivatives was accomplished through intra and self-intermolecular [3 + 2] cycloaddition of azomethine ylides. The chalcone isatin precursors 9a–i required… read more here.

Keywords: oxindole; spiropyrrolidine oxindole; spiropyrrolizidine oxindole; cycloaddition azomethine ... See more keywords

Synthesis of bioactive fluoropyrrolidines via copper(i)-catalysed asymmetric 1,3-dipolar cycloaddition of azomethine ylides

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Published in 2022 at "Chemical Science"

DOI: 10.1039/d1sc04595d

Abstract: Chiral pyrrolidinyl units are important building blocks in biologically active natural products and drugs, and the development of efficient methods for the synthesis of diverse structured pyrrolidine derivatives is of great importance. Meanwhile, incorporating fluorine… read more here.

Keywords: azomethine ylides; cycloaddition azomethine; dipolar cycloaddition; synthesis bioactive ... See more keywords

Catalytic enantioselective intramolecular 1,3-dipolar cycloaddition of azomethine ylides with fluorinated dipolarophiles.

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Published in 2022 at "Chemical communications"

DOI: 10.1039/d2cc02902b

Abstract: An enantioselective synthesis of polycyclic fluorinated pyrrolidines has been achieved by Cu-catalyzed intramolecular 1,3-dipolar cycloaddition of azomethine ylides with fluorinated dipolarophiles. The method displays a wide scope and afforded the desired cycloadducts in high yields… read more here.

Keywords: dipolar cycloaddition; intramolecular dipolar; cycloaddition azomethine; ylides fluorinated ... See more keywords
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Recent advances on (3+2) cycloaddition of Azomethine Ylide.

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Published in 2023 at "New Journal of Chemistry"

DOI: 10.1039/d3nj01018j

Abstract: Nitrogen-containing heterocyclic compounds are some of the most significant that are produced artificially or naturally. These heterocyclic rings are virtually always present in biological systems, from the smallest eukaryotes to... read more here.

Keywords: cycloaddition azomethine; azomethine ylide; chemistry; recent advances ... See more keywords

[3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones

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Published in 2022 at "Royal Society Open Science"

DOI: 10.1098/rsos.211967

Abstract: A synthesis of dispiro derivatives from 5-methylidene-2-chalcogenimidazolones and azomethine ylides generated from isatins and N-substituted α-amino acids has been developed. read more here.

Keywords: ylides methylidene; cycloaddition azomethine; methylidene aryl; halcogen imidazolones ... See more keywords