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技术文章
推荐:QPhos Pd G3@2024技术文献价格已更新
推荐:QPhos Pd G3@2024技术文献价格已更新
别名:QPhos G3 Palladacycle, QPhos Palladacycle
Empirical Formula (Hill Notation):C61H60FeNO3PPdS
CAS号:2021255-91-2
分子量:1080.44
MDL编号:MFCD12911997
形式
powder
特点
generation 3
reaction suitability
core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
reaction type: Cross Couplings
官能团
phosphine
推荐:QPhos Pd G3@2024技术文献价格已更新
说明
一般描述
QPhos Pd G3 is a third generation (G3) Buchwald precatalyst. It is air, moisture and thermally-stable and is highly soluble in a wide range of common organic solvents. It has long life in solutions. Qphos Pd G3 is an excellent reagent for palladium catalyzed cross-coupling reactions. Some of its unique features include lower catalyst loadings, shorter reaction time, efficient formation of the active catalytic species and accurate control of ligand: palladium ratio.
应用
QPhos Pd G3 has been used as a precatalyst for the arylboration of isoprene with regioselectivity . It may also be used for a variety of aminination and etherifications of aryl halides.
其他说明
Technology Spotlight: G3 and G4 Buchwald Precatalysts
Regioselective Arylboration of Isoprene and Its Derivatives by Pd/Cu Cooperative Catalysis
Synthesis of Complex Drug like Molecules by the Use of Highly Functionalized Bench-Stable Organozinc Reagents
Regioselective Arylboration of Isoprene and Its Derivatives by Pd/Cu Cooperative Catalysis
Synthesis of Complex Drug like Molecules by the Use of Highly Functionalized Bench-Stable Organozinc Reagents

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原创作者:上海笃玛生物科技有限公司