Results 81 to 90 of about 16,757 (133)
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Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1973
1. The chloromethyl methyl sulfoxide complex of Pd catalyzes the hydrogenation of the C=C bond of allyl alcohol (AA) and 3-cyclohexenol, and also their rearrangement respectively to propionaldehyde and cyclohexanone. 2. The chloromethyl methyl sulfoxide complex of Rh accelerates the hydrogenation of AA and also its rearrangement, either ...
N M Nazarova +2 more
exaly +3 more sources
1. The chloromethyl methyl sulfoxide complex of Pd catalyzes the hydrogenation of the C=C bond of allyl alcohol (AA) and 3-cyclohexenol, and also their rearrangement respectively to propionaldehyde and cyclohexanone. 2. The chloromethyl methyl sulfoxide complex of Rh accelerates the hydrogenation of AA and also its rearrangement, either ...
N M Nazarova +2 more
exaly +3 more sources
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1973
N M Nazarova +2 more
exaly +2 more sources
N M Nazarova +2 more
exaly +2 more sources
Journal of Organic Chemistry, 2022
Methylene and methyl tricyclic isoquinolinones were selectively prepared using a palladium(II)-catalyzed aerobic aza-Wacker reaction, followed by a base- and temperature-controlled Heck reaction catalyzed by palladium(0).
Li-Yuan Chen +4 more
semanticscholar +1 more source
Methylene and methyl tricyclic isoquinolinones were selectively prepared using a palladium(II)-catalyzed aerobic aza-Wacker reaction, followed by a base- and temperature-controlled Heck reaction catalyzed by palladium(0).
Li-Yuan Chen +4 more
semanticscholar +1 more source
Organic Letters, 2023
In this paper, a convenient synthesis of 2,5-diacylthiophenes and β-acyl allylic methylsulfones from aryl methyl ketones with dimethyl sulfoxide (DMSO) through Selectfluor-promoted cascade cyclization and cross-coupling reactions by simple solvent modification is described. This method enables the formation of new C-C and C-S bonds via the selection of
Hao Lu +6 more
openaire +2 more sources
In this paper, a convenient synthesis of 2,5-diacylthiophenes and β-acyl allylic methylsulfones from aryl methyl ketones with dimethyl sulfoxide (DMSO) through Selectfluor-promoted cascade cyclization and cross-coupling reactions by simple solvent modification is described. This method enables the formation of new C-C and C-S bonds via the selection of
Hao Lu +6 more
openaire +2 more sources
Australian Journal of Chemistry, 1989
The lithium enolates arising by aprotic conjugate addition of lithiated but-2-enyl sulfoxides and a phosphine oxide to cyclopent-2-enone react efficiently with methyl cyanoformate to give the corresponding methyl 5-oxocyclopentanecarboxylates in good yields.
RK Haynes, AG Katsifis
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The lithium enolates arising by aprotic conjugate addition of lithiated but-2-enyl sulfoxides and a phosphine oxide to cyclopent-2-enone react efficiently with methyl cyanoformate to give the corresponding methyl 5-oxocyclopentanecarboxylates in good yields.
RK Haynes, AG Katsifis
openaire +1 more source
Chemischer Informationsdienst, 1986
AbstractThe allyl methyl sulfoxides (Ic)‐(If) are synthesized from the sulfenylchlorides (IV) and allyl alcohol (V).
J. HOLOCH, W. SUNDERMEYER
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AbstractThe allyl methyl sulfoxides (Ic)‐(If) are synthesized from the sulfenylchlorides (IV) and allyl alcohol (V).
J. HOLOCH, W. SUNDERMEYER
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Chemische Berichte, 1986
AbstractDie Allyl‐methyl‐sulfoxide R1R2R3CS(O)CH2CHCH2 1a–7a (R1, R2, R3 = H, F, Cl, CF3) sowie die entsprechenden Sulfone 1b–7b wurden dargestellt. Die an der Methylgruppe substituierten Sulfoxide stehen im Gleichgewicht mit Sulfensäure‐allylestern R1R2R3CSOCH2CHCH2 in Abhängigkeit von der Temperatur und der Art der Substitution.
Jan Holoch, Wolfgang Sundermeyer
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AbstractDie Allyl‐methyl‐sulfoxide R1R2R3CS(O)CH2CHCH2 1a–7a (R1, R2, R3 = H, F, Cl, CF3) sowie die entsprechenden Sulfone 1b–7b wurden dargestellt. Die an der Methylgruppe substituierten Sulfoxide stehen im Gleichgewicht mit Sulfensäure‐allylestern R1R2R3CSOCH2CHCH2 in Abhängigkeit von der Temperatur und der Art der Substitution.
Jan Holoch, Wolfgang Sundermeyer
openaire +1 more source

