Murphy, Jaclyn M.’s team published research in Organic Letters in 9 | CAS: 929626-18-6

Organic Letters published new progress about 929626-18-6. 929626-18-6 belongs to ethers-buliding-blocks, auxiliary class Boronic acid and ester,Benzene,Ester,Boronic Acids,Boronic Acids,Boronic acid and ester, name is (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, and the molecular formula is C9H11BO4, Application In Synthesis of 929626-18-6.

Murphy, Jaclyn M. published the artcileOne-Pot Synthesis of Arylboronic Acids and Aryl Trifluoroborates by Ir-Catalyzed Borylation of Arenes, Application In Synthesis of 929626-18-6, the publication is Organic Letters (2007), 9(5), 757-760, database is CAplus and MEDLINE.

The synthesis of arylboronic acids and aryl trifluoroborates in a one-pot sequence by Ir-catalyzed borylation of arenes is reported. To prepare the arylboronic acids, the Ir-catalyzed borylation is followed by oxidative cleavage of the boronic ester with NaIO4 and to prepare the aryltrifluoroborate, the Ir-catalyzed borylation is followed by displacement of pinacol by KHF2. These two-step sequences give products that are more reactive toward subsequent chem. than the initially formed pinacol boronates.

Organic Letters published new progress about 929626-18-6. 929626-18-6 belongs to ethers-buliding-blocks, auxiliary class Boronic acid and ester,Benzene,Ester,Boronic Acids,Boronic Acids,Boronic acid and ester, name is (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, and the molecular formula is C9H11BO4, Application In Synthesis of 929626-18-6.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Furuya, Takeru’s team published research in Organic Letters in 11 | CAS: 929626-18-6

Organic Letters published new progress about 929626-18-6. 929626-18-6 belongs to ethers-buliding-blocks, auxiliary class Boronic acid and ester,Benzene,Ester,Boronic Acids,Boronic Acids,Boronic acid and ester, name is (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, and the molecular formula is C9H11BO4, Computed Properties of 929626-18-6.

Furuya, Takeru published the artcileFluorination of Boronic Acids Mediated by Silver(I) Triflate, Computed Properties of 929626-18-6, the publication is Organic Letters (2009), 11(13), 2860-2863, database is CAplus and MEDLINE.

A regiospecific Ag-mediated fluorination reaction of aryl- and alkenylboronic acids and esters is reported. The fluorination reaction uses com. available reagents, does not require the addition of exogenous ligands, and can be performed on a multigram scale. This report discloses the first practical reaction sequence from arylboronic acid to aryl fluorides.

Organic Letters published new progress about 929626-18-6. 929626-18-6 belongs to ethers-buliding-blocks, auxiliary class Boronic acid and ester,Benzene,Ester,Boronic Acids,Boronic Acids,Boronic acid and ester, name is (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, and the molecular formula is C9H11BO4, Computed Properties of 929626-18-6.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Tzschucke, C. Christoph’s team published research in Organic Letters in 9 | CAS: 929626-18-6

Organic Letters published new progress about 929626-18-6. 929626-18-6 belongs to ethers-buliding-blocks, auxiliary class Boronic acid and ester,Benzene,Ester,Boronic Acids,Boronic Acids,Boronic acid and ester, name is (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, and the molecular formula is C6H3BF4O2, HPLC of Formula: 929626-18-6.

Tzschucke, C. Christoph published the artcileArenes to anilines and aryl ethers by sequential iridium-catalyzed borylation and copper-catalyzed coupling, HPLC of Formula: 929626-18-6, the publication is Organic Letters (2007), 9(5), 761-764, database is CAplus and MEDLINE.

N-Alkyl- and N-arylanilines were synthesized from arenes by a two-step sequence of iridium-catalyzed borylation and copper-catalyzed coupling with amines. Diaryl ethers were obtained by a related sequence of arene borylation, followed by coupling with phenols. In particular, 3,5-disubstituted arylamines and aryl ethers were prepared by initiating this sequence with meta-substituted arenes.

Organic Letters published new progress about 929626-18-6. 929626-18-6 belongs to ethers-buliding-blocks, auxiliary class Boronic acid and ester,Benzene,Ester,Boronic Acids,Boronic Acids,Boronic acid and ester, name is (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, and the molecular formula is C6H3BF4O2, HPLC of Formula: 929626-18-6.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Huang, Chenghong’s team published research in Journal of the American Chemical Society in 133 | CAS: 929626-18-6

Journal of the American Chemical Society published new progress about 929626-18-6. 929626-18-6 belongs to ethers-buliding-blocks, auxiliary class Boronic acid and ester,Benzene,Ester,Boronic Acids,Boronic Acids,Boronic acid and ester, name is (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, and the molecular formula is C9H11BO4, Recommanded Product: (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid.

Huang, Chenghong published the artcileSilver-Mediated Trifluoromethoxylation of Aryl Stannanes and Arylboronic Acids, Recommanded Product: (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, the publication is Journal of the American Chemical Society (2011), 133(34), 13308-13310, database is CAplus and MEDLINE.

A silver-mediated cross-coupling of trifluoromethoxide with aryl stannanes and arylboronic acids to give aryl trifluoromethyl ethers, e.g., I, is reported. This is the first report of a transition-metal-mediated Caryl-OCF3 bond formation.

Journal of the American Chemical Society published new progress about 929626-18-6. 929626-18-6 belongs to ethers-buliding-blocks, auxiliary class Boronic acid and ester,Benzene,Ester,Boronic Acids,Boronic Acids,Boronic acid and ester, name is (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid, and the molecular formula is C9H11BO4, Recommanded Product: (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem