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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%…
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Keywords:
asymmetric dipolar;
azomethine ylides;
catalysed asymmetric;
ferrocene derived ... See more keywords
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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…
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Keywords:
formal cycloaddition;
imines azlactones;
azomethine imines;
cycloaddition azomethine ... See more keywords
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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…
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Keywords:
nitrile oxides;
azomethine imines;
cycloaddition azomethine;
imines situ ... See more keywords
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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…
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Keywords:
oxindole;
spiropyrrolidine oxindole;
spiropyrrolizidine oxindole;
cycloaddition azomethine ... See more keywords
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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…
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Keywords:
azomethine ylides;
cycloaddition azomethine;
dipolar cycloaddition;
synthesis bioactive ... See more keywords
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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…
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Keywords:
dipolar cycloaddition;
intramolecular dipolar;
cycloaddition azomethine;
ylides fluorinated ... See more keywords
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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...
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Keywords:
cycloaddition azomethine;
azomethine ylide;
chemistry;
recent advances ... See more keywords
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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.
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Keywords:
ylides methylidene;
cycloaddition azomethine;
methylidene aryl;
halcogen imidazolones ... See more keywords