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Published in 2020 at "Organic letters"
DOI: 10.1021/acs.orglett.0c01821
Abstract: A metal-free electrochemical intramolecular C(sp2)-H amination using iodine as a mediator was developed. This method enables a switchable synthesis of indoline and indole derivatives, respectively, from easily available 2-vinyl anilines.
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Keywords:
switchable synthesis;
iodine mediated;
sp2 amination;
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Published in 2024 at "Organic letters"
DOI: 10.1021/acs.orglett.4c01437
Abstract: Here, we present a versatile, silver-catalyzed multi-auto-tandem reaction involving enamines, alkynals, and nucleophiles, utilizing the highly reactive intermediate azafulvenium. This method allows for flexible and switchable regiodivergent reactions through either intermolecular or intramolecular nucleophilic attacks,…
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Keywords:
site specifically;
synthesis site;
site;
azafulvenium ... See more keywords
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Published in 2018 at "ACS Catalysis"
DOI: 10.1021/acscatal.8b02530
Abstract: The use of earth-abundant transition metals as a noble metal replacement in catalysis is especially interesting if different catalytic reactivity is observed. We report, here, on the selective manganese-catalyzed base-switchable synthesis of N-alkylated amines or…
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Keywords:
hydrogen;
manganese catalyzed;
base switchable;
base ... See more keywords
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Published in 2023 at "Molecules"
DOI: 10.3390/molecules28114347
Abstract: Regio- and stereoselective switchable synthesis of (E)- and (Z)-N-carbonylvinylated pyrazoles is first developed by using the Michael addition reaction of pyrazoles and conjugated carbonyl alkynes. Ag2CO3 plays a key role in the switchable synthesis of…
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Keywords:
synthesis carbonylvinylated;
carbonylvinylated pyrazoles;
regio stereoselective;
stereoselective switchable ... See more keywords