(11bS)-2,6-Bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin

97%

Reagent Code: #232658
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CAS Number 2757287-50-4

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Weight 784.96 g/mol
Formula C₅₀H₅₇O₆P
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation and C–C bond-forming reactions. Its sterically bulky tert-butyl and methoxy substituents enhance stereocontrol, making it effective in promoting high enantioselectivity with transition metal catalysts. Commonly employed in pharmaceutical synthesis where precise chirality is critical. Also utilized in research for developing new asymmetric methodologies due to its stable phosphorus center and rigid dinaphthyl backbone.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,170.00
inventory 250mg
10-20 days ฿23,440.00
inventory 1g
10-20 days ฿72,630.00

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(11bS)-2,6-Bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation and C–C bond-forming reactions. Its sterically bulky tert-butyl and methoxy substituents enhance stereocontrol, making it effective in promoting high enantioselectivity with transition metal catalysts. Commonly employed in pharmaceutical synthesis where precise chirality is critical. Also utilized in research for developing new asymmetric methodologies due to its stable phosphorus cente

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation and C–C bond-forming reactions. Its sterically bulky tert-butyl and methoxy substituents enhance stereocontrol, making it effective in promoting high enantioselectivity with transition metal catalysts. Commonly employed in pharmaceutical synthesis where precise chirality is critical. Also utilized in research for developing new asymmetric methodologies due to its stable phosphorus center and rigid dinaphthyl backbone.

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