(S)-1,1′-Binaphthyl-2,2′-diyl bis((1S)-1-phenylethyl)phosphoramidite copper(I) triflate

≥95%

Reagent Code: #234200
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CAS Number 1393481-66-7

science Other reagents with same CAS 1393481-66-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 752.22 g/mol
Formula C₃₇H₃₀CuF₃NO₅PS
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective coupling reactions. It facilitates the formation of carbon–carbon and carbon–heteroatom bonds with high enantioselectivity. Commonly applied in copper-catalyzed conjugate additions, allylic substitutions, and cyclopropanations where precise stereochemical control is required. The ligand environment enhances reactivity and selectivity, making it valuable in pharmaceutical and fine chemical synthesis for producing single-enantiomer compounds. Stable under inert conditions and effective at low catalyst loadings, it supports efficient and scalable transformations.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,170.00
(S)-1,1′-Binaphthyl-2,2′-diyl bis((1S)-1-phenylethyl)phosphoramidite copper(I) triflate
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Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective coupling reactions. It facilitates the formation of carbon–carbon and carbon–heteroatom bonds with high enantioselectivity. Commonly applied in copper-catalyzed conjugate additions, allylic substitutions, and cyclopropanations where precise stereochemical control is required. The ligand environment enhances reactivity and selectivity, making it valuable in pharmaceutical and fine chemical synthesis for producing single-en

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective coupling reactions. It facilitates the formation of carbon–carbon and carbon–heteroatom bonds with high enantioselectivity. Commonly applied in copper-catalyzed conjugate additions, allylic substitutions, and cyclopropanations where precise stereochemical control is required. The ligand environment enhances reactivity and selectivity, making it valuable in pharmaceutical and fine chemical synthesis for producing single-enantiomer compounds. Stable under inert conditions and effective at low catalyst loadings, it supports efficient and scalable transformations.

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