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4-BROMOPHENYLBORONIC ACID, >=95.0%
Кат. №: B75956-5G
Производитель: Sigma-Aldrich
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Товар оформляется под заказ
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4-BROMOPHENYLBORONIC ACID, >=95.0%
Main image
Кат. №: B75956-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
4-BROMOPHENYLBORONIC ACID, >=95.0%
Кат. №: B75956-5G
Производитель: Sigma-Aldrich
Кол-во:
Цена по запросу
Товар оформляется под заказ
Description Application Reagent used for • Palladium catalyzed Suzuki-Miyaura cross-couplings • Pd(II)-catalyzed diastereoselective conjugate additions • Palladium-catalyzed stereoselective Heck-type reaction of allylic esters with arylboronic acids • Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence • Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides • Pd-catalyzed arylative cyclization of alkyne-tethered enals or enones via carbopalladation of alkynes • Copper-catalyzed cross-couplings Reagent used in Preparation of • Gallate-based obovatol analogs with potential anti-tumor activity • Protein modulators and enzymatic and kinase inhibitors Packaging 5 g in glass bottle Other Notes Contains varying amounts of anhydride
Related Categories
Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids, Organometallic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.
Description Application Reagent used for • Palladium catalyzed Suzuki-Miyaura cross-couplings • Pd(II)-catalyzed diastereoselective conjugate additions • Palladium-catalyzed stereoselective Heck-type reaction of allylic esters with arylboronic acids • Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence • Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides • Pd-catalyzed arylative cyclization of alkyne-tethered enals or enones via carbopalladation of alkynes • Copper-catalyzed cross-couplings Reagent used in Preparation of • Gallate-based obovatol analogs with potential anti-tumor activity • Protein modulators and enzymatic and kinase inhibitors Packaging 5 g in glass bottle Other Notes Contains varying amounts of anhydride
Related Categories
Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids, Organometallic Reagents More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.