(3AS,3'aS,7aS,7'aS)-2,2'-[[(1R,3R)-1,3-Dimethyl-1,3-propanediyl]bis(oxy)]bis[octahydro-1,3-diphenyl-1H-1,3,2-benzodiazaphosphole]
98%
Reagent
Code: #138272
CAS Number
1384535-76-5
blur_circular Chemical Specifications
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Molecular Information
Weight
692.81 g/mol
Formula
C₄₁H₅₀N₄O₂P₂
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Registry Numbers
MDL Number
MFCD32173534
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Storage & Handling
Storage
Room temperature, inert gas
description Product Description
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereoselectivity in carbon-carbon bond-forming reactions such as hydrogenation, allylic alkylation, and cross-coupling processes. Its rigid, bidentate structure enhances metal-ligand coordination, improving catalytic efficiency and enantiomeric excess in the synthesis of pharmaceuticals and fine chemicals. Commonly employed with palladium, rhodium, or ruthenium complexes, it enables the production of single-enantiomer compounds important in drug development and agrochemicals.
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(3AS,3'aS,7aS,7'aS)-2,2'-[[(1R,3R)-1,3-Dimethyl-1,3-propanediyl]bis(oxy)]bis[octahydro-1,3-diphenyl-1H-1,3,2-benzodiazaphosphole]
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereoselectivity in carbon-carbon bond-forming reactions such as hydrogenation, allylic alkylation, and cross-coupling processes. Its rigid, bidentate structure enhances metal-ligand coordination, improving catalytic efficiency and enantiomeric excess in the synthesis of pharmaceuticals and fine chemicals. Commonly employed with palladium, rhodium, or ruthenium complexes, it enables the production of single-enantiomer compounds important in drug development and agrochemicals.
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