Tetrakis[(S)-()-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)

98%

Reagent Code: #244876
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CAS Number 909389-99-7

science Other reagents with same CAS 909389-99-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1559.32 g/mol
Formula C₈₀H₈₀N₄O₁₆Rh₂
badge Registry Numbers
MDL Number MFCD09839140
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a highly efficient chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H functionalization reactions. It enables the selective insertion of carbenoids into C–H bonds with excellent stereocontrol, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products. Its adamantyl and phthalimido groups enhance steric bulk and electronic properties, contributing to high enantioselectivity and catalyst stability under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿28,250.00
inventory 250mg
10-20 days ฿70,650.00
inventory 100mg
10-20 days ฿38,650.00

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Tetrakis[(S)-()-(1-adamantyl)-(N-phthalimido)acetato]dirhodium(II)
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Used as a highly efficient chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H functionalization reactions. It enables the selective insertion of carbenoids into C–H bonds with excellent stereocontrol, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products. Its adamantyl and phthalimido groups enhance steric bulk and electronic properties, contributing to high enantioselectivity and catalyst stability under various reacti

Used as a highly efficient chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H functionalization reactions. It enables the selective insertion of carbenoids into C–H bonds with excellent stereocontrol, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products. Its adamantyl and phthalimido groups enhance steric bulk and electronic properties, contributing to high enantioselectivity and catalyst stability under various reaction conditions.

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