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Organic Chemistry Portal

@organic_portal

The Organic Chemistry Portal offers an overview of recent topics, interesting reactions, and information on important chemicals for organic chemists

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linkhttps://www.organic-chemistry.org calendar_today08-10-2018 22:58:58

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organic-chemistry.org/abstracts/lit8… A phosphazene base-catalyzed intramolecular hydroamidation of amide alkenes provides cyclic amides.

organic-chemistry.org/abstracts/lit8…
A phosphazene base-catalyzed intramolecular hydroamidation of amide alkenes provides cyclic amides.
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organic-chemistry.org/abstracts/lit9… Hydrogen-bonded aggregates of B(C6F5)3 catalyze a reaction of aromatic amines with sulfoxonium ylides

organic-chemistry.org/abstracts/lit9…
Hydrogen-bonded aggregates of B(C6F5)3 catalyze a reaction of aromatic amines with sulfoxonium ylides
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organic-chemistry.org/abstracts/lit4… A photochemically catalyzed isomerization of the thermodynamic E-alkene to the less stable Z-isomer

organic-chemistry.org/abstracts/lit4…
A photochemically catalyzed isomerization of the thermodynamic E-alkene to the less stable Z-isomer
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organic-chemistry.org/abstracts/lit7… Cross-coupling reactions of iodoarenes with trifluoromethylsilanes smoothly provide trifluoromethylated aromatics in good yields.

organic-chemistry.org/abstracts/lit7…
Cross-coupling reactions of iodoarenes with trifluoromethylsilanes smoothly provide trifluoromethylated aromatics in good yields.
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organic-chemistry.org/abstracts/lit9… Copper-catalyzed amination of aryl chlorides proceeds at low temperatures and with a broad scope

organic-chemistry.org/abstracts/lit9…
Copper-catalyzed amination of aryl chlorides proceeds at low temperatures and with a broad scope
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organic-chemistry.org/abstracts/lit7… A practical electrochemical desulfurative cyclization of isothiocyanates and α-amino ketones provides diverse oxazol-2-amine derivatives

organic-chemistry.org/abstracts/lit7…
A practical electrochemical desulfurative cyclization of isothiocyanates and α-amino ketones provides diverse oxazol-2-amine derivatives
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organic-chemistry.org/abstracts/lit8… A photochemically induced nickel-catalyzed radical cross-coupling of phthalimido trifluoroethanol with aryl bromides

organic-chemistry.org/abstracts/lit8…
A photochemically induced nickel-catalyzed radical cross-coupling of phthalimido trifluoroethanol with aryl bromides
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organic-chemistry.org/abstracts/lit4… Ni(ClO4)2·6H2O can be used as a Lewis acid catalyst for nucleophilic amine ring-opening cyclizations of donor-acceptor (D-A) cyclopropanes

organic-chemistry.org/abstracts/lit4…
Ni(ClO4)2·6H2O can be used as a Lewis acid catalyst for nucleophilic amine ring-opening cyclizations of donor-acceptor (D-A) cyclopropanes
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organic-chemistry.org/abstracts/lit4… An alkenylation of alkyl electrophiles using nearly stoichiometric amounts of air- and moisture-stable potassium organotrifluoroborates

organic-chemistry.org/abstracts/lit4…
An alkenylation of alkyl electrophiles using nearly stoichiometric amounts of air- and moisture-stable potassium organotrifluoroborates
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organic-chemistry.org/abstracts/lit9… A copper(0)-catalyzed reductive coupling of disulfurating reagents with (hetero)aryl/alkyl halides provides disulfides.

organic-chemistry.org/abstracts/lit9…
A copper(0)-catalyzed reductive coupling of disulfurating reagents with (hetero)aryl/alkyl halides provides disulfides.
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organic-chemistry.org/abstracts/lit4… Treatment of pyridine N-oxides with 4-toluene sulfonyl chloride and sodium azide in toluene at elevated temperature

organic-chemistry.org/abstracts/lit4…
Treatment of pyridine N-oxides with 4-toluene sulfonyl chloride and sodium azide in toluene at elevated temperature
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organic-chemistry.org/abstracts/lit4… A thiazolium precatalyst facilitates electrochemical oxidation of thiolate anions, leading to deleterious formation of disulfide byproducts.

organic-chemistry.org/abstracts/lit4…
A thiazolium precatalyst facilitates electrochemical oxidation of thiolate anions, leading to deleterious formation of disulfide byproducts.