Home Chemistry Organic Building Blocks Aryls 3,3'-Diphenyl-5,5',6,6',7,7',8,8'-Octahydro-1,1'-Binaphthalene
Transition Metal Catalysis: BINAP is widely used as a chiral ligand in transition metal-catalyzed reactions, such as asymmetric hydrogenation, asymmetric Heck reactions, asymmetric Suzuki-Miyaura coupling, and asymmetric allylation. In these reactions, BINAP helps control the stereochemistry of the products.
Asymmetric Hydrogenation: BINAP is particularly famous for its role in asymmetric hydrogenation reactions, where it helps convert prochiral substrates into chiral products with high enantiomeric purity.
Palladium-Catalyzed Cross-Coupling: BINAP can be used in palladium-catalyzed cross-coupling reactions, leading to the formation of various aryl and heteroaryl compounds with high enantioselectivity.
Rhodium-Catalyzed Asymmetric Hydroformylation: BINAP can be employed in rhodium-catalyzed asymmetric hydroformylation reactions to produce chiral aldehydes.
Lewis Acid Catalysis: BINAP can also be used in Lewis acid-catalyzed reactions, especially for the activation of carbonyl compounds.
Suzuki-Miyaura Coupling: BINAP can be applied in Suzuki-Miyaura coupling reactions for the synthesis of biaryl compounds with high enantiomeric excess.
Metal-Catalyzed Cycloisomerizations: BINAP can be used in metal-catalyzed cycloisomerization reactions, leading to the formation of complex, chiral cyclic compounds.
Cyclopalladation: BINAP can coordinate to palladium in such a way that it can undergo cyclopalladation reactions, which are important in the synthesis of certain organic compounds.
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(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis(2,4,6-trimethylphenyl)-[1,1'-binaphthalene]-2,2'-diol
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(R)-3,3'-Bis(4-(trifluoromethyl)phenyl)-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
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(R)-3,3'-Bis(4-methoxyphenyl)-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
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(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis(4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol
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(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-diphenyl-[1,1'-binaphthalene]-2,2'-diol
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(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-diphenyl-[1,1'-binaphthalene]-2,2'-diol
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(R)-3,3'-Dimesityl-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
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(S)-3,3'-Bis3,5-bis(trifluoromethyl)phenyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
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(R)-3,3'-Bis3,5-bis(trifluoromethyl)phenyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
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(S)-3,3'-Bis(3,5-dimethylphenyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
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(R)-3,3'-Bis(3,5-dimethylphenyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
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(S)-3,3'-Bis(4-nitrophenyl)-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
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(S)-3,3'-Bis(4-(trifluoromethyl)phenyl)-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
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