Organic Chemistry Portal
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The Organic Chemistry Portal - For daily updates please visit https://www.organic-chemistry.org/abstracts/ and check out https://www.organic-chemistry.org/info/linking/
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A β-boron effect accounts for high regioselectivity in electrophilic addition reactions to allylic MIDA (N-methyliminodiacetic acid) boronates.
A β-boron effect accounts for high regioselectivity in electrophilic addition reactions to allylic MIDA (N-methyliminodiacetic acid) boronates.
November 14, 2025 at 12:14 PM
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A β-boron effect accounts for high regioselectivity in electrophilic addition reactions to allylic MIDA (N-methyliminodiacetic acid) boronates.
A β-boron effect accounts for high regioselectivity in electrophilic addition reactions to allylic MIDA (N-methyliminodiacetic acid) boronates.
www.organic-chemistry.org/abstracts/li...
A highly enantioselective silicon-directed Nazarov reaction is cooperatively catalyzed by a Lewis acid and a chiral Brønsted acid.
A highly enantioselective silicon-directed Nazarov reaction is cooperatively catalyzed by a Lewis acid and a chiral Brønsted acid.
November 14, 2025 at 12:12 PM
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A highly enantioselective silicon-directed Nazarov reaction is cooperatively catalyzed by a Lewis acid and a chiral Brønsted acid.
A highly enantioselective silicon-directed Nazarov reaction is cooperatively catalyzed by a Lewis acid and a chiral Brønsted acid.
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Quantitative oxidative conversion of thiols to disulfides was effected by aqueous 30% H2O2 in trifluoroethanol
Quantitative oxidative conversion of thiols to disulfides was effected by aqueous 30% H2O2 in trifluoroethanol
November 14, 2025 at 12:09 PM
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Quantitative oxidative conversion of thiols to disulfides was effected by aqueous 30% H2O2 in trifluoroethanol
Quantitative oxidative conversion of thiols to disulfides was effected by aqueous 30% H2O2 in trifluoroethanol
www.organic-chemistry.org/abstracts/li...
An operationally simple and efficient strategy for the synthesis of substituted tetrahydrofurans from readily available cis-butene-1,4-diol
An operationally simple and efficient strategy for the synthesis of substituted tetrahydrofurans from readily available cis-butene-1,4-diol
November 14, 2025 at 12:06 PM
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An operationally simple and efficient strategy for the synthesis of substituted tetrahydrofurans from readily available cis-butene-1,4-diol
An operationally simple and efficient strategy for the synthesis of substituted tetrahydrofurans from readily available cis-butene-1,4-diol
www.organic-chemistry.org/abstracts/li...
A Julia-Kocienski reaction of 2,2-dimethoxyethyl 1-phenyl-1H-tetrazol-5-yl (PT) sulfone with various aldehydes
A Julia-Kocienski reaction of 2,2-dimethoxyethyl 1-phenyl-1H-tetrazol-5-yl (PT) sulfone with various aldehydes
November 14, 2025 at 12:03 PM
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A Julia-Kocienski reaction of 2,2-dimethoxyethyl 1-phenyl-1H-tetrazol-5-yl (PT) sulfone with various aldehydes
A Julia-Kocienski reaction of 2,2-dimethoxyethyl 1-phenyl-1H-tetrazol-5-yl (PT) sulfone with various aldehydes
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A microwave-promoted, solvent-free Biginelli three-component cyclocondensation
A microwave-promoted, solvent-free Biginelli three-component cyclocondensation
November 14, 2025 at 11:56 AM
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A microwave-promoted, solvent-free Biginelli three-component cyclocondensation
A microwave-promoted, solvent-free Biginelli three-component cyclocondensation
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Excited-state palladium-catalyzed alkylations of quinoxalinones
Excited-state palladium-catalyzed alkylations of quinoxalinones
November 14, 2025 at 11:54 AM
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Excited-state palladium-catalyzed alkylations of quinoxalinones
Excited-state palladium-catalyzed alkylations of quinoxalinones
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A metal-free CH [5 + 1] carbonylative annulation of 2-alkenyl/pyrrolylanilines with dioxazolones
A metal-free CH [5 + 1] carbonylative annulation of 2-alkenyl/pyrrolylanilines with dioxazolones
November 14, 2025 at 11:52 AM
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A metal-free CH [5 + 1] carbonylative annulation of 2-alkenyl/pyrrolylanilines with dioxazolones
A metal-free CH [5 + 1] carbonylative annulation of 2-alkenyl/pyrrolylanilines with dioxazolones
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Several alcohols were smoothly and practically sulfonylated.
Several alcohols were smoothly and practically sulfonylated.
November 13, 2025 at 11:46 AM
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Several alcohols were smoothly and practically sulfonylated.
Several alcohols were smoothly and practically sulfonylated.
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An organo-photocatalytic sulfonylimination of alkenes using readily available N-sulfonyl ketimines
An organo-photocatalytic sulfonylimination of alkenes using readily available N-sulfonyl ketimines
November 13, 2025 at 11:43 AM
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An organo-photocatalytic sulfonylimination of alkenes using readily available N-sulfonyl ketimines
An organo-photocatalytic sulfonylimination of alkenes using readily available N-sulfonyl ketimines
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Eu(OTf)3 catalyzes a transsulfinamidation of primary sulfinamides with alkyl, aryl, and heterocyclic amines
Eu(OTf)3 catalyzes a transsulfinamidation of primary sulfinamides with alkyl, aryl, and heterocyclic amines
November 13, 2025 at 11:41 AM
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Eu(OTf)3 catalyzes a transsulfinamidation of primary sulfinamides with alkyl, aryl, and heterocyclic amines
Eu(OTf)3 catalyzes a transsulfinamidation of primary sulfinamides with alkyl, aryl, and heterocyclic amines
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Various aromatic and aliphatic nitriles were prepared in high yields in a direct one-pot process
Various aromatic and aliphatic nitriles were prepared in high yields in a direct one-pot process
November 13, 2025 at 11:37 AM
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Various aromatic and aliphatic nitriles were prepared in high yields in a direct one-pot process
Various aromatic and aliphatic nitriles were prepared in high yields in a direct one-pot process
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Low loadings of commercially available lithium triethylborohydride catalyze the hydroamination of various carbodiimides.
Low loadings of commercially available lithium triethylborohydride catalyze the hydroamination of various carbodiimides.
November 13, 2025 at 11:35 AM
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Low loadings of commercially available lithium triethylborohydride catalyze the hydroamination of various carbodiimides.
Low loadings of commercially available lithium triethylborohydride catalyze the hydroamination of various carbodiimides.
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An iridium complex catalyzes an environmentally friendly, efficient, and facile one-pot transfer hydrogenation of C=C bond of enones and reductive amination
An iridium complex catalyzes an environmentally friendly, efficient, and facile one-pot transfer hydrogenation of C=C bond of enones and reductive amination
November 13, 2025 at 11:33 AM
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An iridium complex catalyzes an environmentally friendly, efficient, and facile one-pot transfer hydrogenation of C=C bond of enones and reductive amination
An iridium complex catalyzes an environmentally friendly, efficient, and facile one-pot transfer hydrogenation of C=C bond of enones and reductive amination
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More Info: www.organic-chemistry.org/info/present...
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More Info: www.organic-chemistry.org/info/present...
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November 12, 2025 at 10:50 AM
Ad: Vapourtec - Peptide-Builder
More Info: www.organic-chemistry.org/info/present...
Peptide-Builder is a compact, fully automated, lab-scale synthesizer that transforms solid-phase peptide synthesis (SPPS) through advanced flow chemistry technology
More Info: www.organic-chemistry.org/info/present...
Peptide-Builder is a compact, fully automated, lab-scale synthesizer that transforms solid-phase peptide synthesis (SPPS) through advanced flow chemistry technology
www.organic-chemistry.org/namedreactio...
Pinacol Coupling Reaction - An overview and some recently published methods
Pinacol Coupling Reaction - An overview and some recently published methods
November 12, 2025 at 10:49 AM
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Pinacol Coupling Reaction - An overview and some recently published methods
Pinacol Coupling Reaction - An overview and some recently published methods
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Primary and secondary trimethylsilyl and tetrahydropyranyl (THP) ethers are converted to their carbonyl compounds efficiently
Primary and secondary trimethylsilyl and tetrahydropyranyl (THP) ethers are converted to their carbonyl compounds efficiently
November 12, 2025 at 10:38 AM
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Primary and secondary trimethylsilyl and tetrahydropyranyl (THP) ethers are converted to their carbonyl compounds efficiently
Primary and secondary trimethylsilyl and tetrahydropyranyl (THP) ethers are converted to their carbonyl compounds efficiently
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Pd/Cu-catalyzed coupling and boration of acyl chlorides with alkynes and B2pin2
Pd/Cu-catalyzed coupling and boration of acyl chlorides with alkynes and B2pin2
November 12, 2025 at 10:33 AM
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Pd/Cu-catalyzed coupling and boration of acyl chlorides with alkynes and B2pin2
Pd/Cu-catalyzed coupling and boration of acyl chlorides with alkynes and B2pin2
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Using a cinchona squaramide-based organocatalyst for an enantioselective intramolecular oxa-Michael reaction of enones as well as α,β-unsaturated esters
Using a cinchona squaramide-based organocatalyst for an enantioselective intramolecular oxa-Michael reaction of enones as well as α,β-unsaturated esters
November 12, 2025 at 10:30 AM
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Using a cinchona squaramide-based organocatalyst for an enantioselective intramolecular oxa-Michael reaction of enones as well as α,β-unsaturated esters
Using a cinchona squaramide-based organocatalyst for an enantioselective intramolecular oxa-Michael reaction of enones as well as α,β-unsaturated esters
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Chemoselective dithioacetalization of aromatic- and α,β-unsaturated aldehydes
Chemoselective dithioacetalization of aromatic- and α,β-unsaturated aldehydes
November 11, 2025 at 10:32 AM
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Chemoselective dithioacetalization of aromatic- and α,β-unsaturated aldehydes
Chemoselective dithioacetalization of aromatic- and α,β-unsaturated aldehydes
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Visible light mediates a P-H insertion reaction between acylsilanes and H-phosphorus oxides
Visible light mediates a P-H insertion reaction between acylsilanes and H-phosphorus oxides
November 11, 2025 at 10:29 AM
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Visible light mediates a P-H insertion reaction between acylsilanes and H-phosphorus oxides
Visible light mediates a P-H insertion reaction between acylsilanes and H-phosphorus oxides
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A diaminocyclopentadienone ruthenium tricarbonyl complex catalyzes the synthesis of mono- or dialkylated acyl hydrazide compounds
A diaminocyclopentadienone ruthenium tricarbonyl complex catalyzes the synthesis of mono- or dialkylated acyl hydrazide compounds
November 11, 2025 at 10:26 AM
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A diaminocyclopentadienone ruthenium tricarbonyl complex catalyzes the synthesis of mono- or dialkylated acyl hydrazide compounds
A diaminocyclopentadienone ruthenium tricarbonyl complex catalyzes the synthesis of mono- or dialkylated acyl hydrazide compounds
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The combination of Fe(III)/NaI catalyzes a very simple and mild oxidative coupling of thiols
The combination of Fe(III)/NaI catalyzes a very simple and mild oxidative coupling of thiols
November 11, 2025 at 10:23 AM
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The combination of Fe(III)/NaI catalyzes a very simple and mild oxidative coupling of thiols
The combination of Fe(III)/NaI catalyzes a very simple and mild oxidative coupling of thiols
www.organic-chemistry.org/abstracts/li...
A palladium(0)-catalyzed defluorosilylation of β,β-difluoroacrylates provides tetrasubstituted vinylsilanes
A palladium(0)-catalyzed defluorosilylation of β,β-difluoroacrylates provides tetrasubstituted vinylsilanes
November 11, 2025 at 10:21 AM
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A palladium(0)-catalyzed defluorosilylation of β,β-difluoroacrylates provides tetrasubstituted vinylsilanes
A palladium(0)-catalyzed defluorosilylation of β,β-difluoroacrylates provides tetrasubstituted vinylsilanes
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The use of secondary amines and NXS (X = Cl, Br, I) enables an unprecedented copper-catalyzed oxidative aminohalogenation of electron-deficient maleimides.
The use of secondary amines and NXS (X = Cl, Br, I) enables an unprecedented copper-catalyzed oxidative aminohalogenation of electron-deficient maleimides.
November 11, 2025 at 10:19 AM
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The use of secondary amines and NXS (X = Cl, Br, I) enables an unprecedented copper-catalyzed oxidative aminohalogenation of electron-deficient maleimides.
The use of secondary amines and NXS (X = Cl, Br, I) enables an unprecedented copper-catalyzed oxidative aminohalogenation of electron-deficient maleimides.