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544461-38-3

544461-38-3 Structure

544461-38-3 Structure
IdentificationBack Directory
[Name]

(S,S)-F-BINAPHANE
[CAS]

544461-38-3
[Synonyms]

(S,S)-F-BINAPHANE
1,1'-Bis[(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino]ferrocene
1,1'-Bis{(S)-4,5-dihydro-3H-binaphtho[1,2-c:2',1'-e]phosphino}ferrocene, Min. 98% (S,S)-f-Binaphane
1,1μ-Bis[(S)-4,5-dihydro-3H-binaphtho[2,1-c:1μ,2μ-e]phosphepino]ferrocene, 1,1μ-Bis[(11bs)-3,5-dihydro-4H-dinaphtho[2,1-c:1μ,2μ-e]phosphenpin-4yl]ferrocene
[Molecular Formula]

2C27H20P.Fe
[MDL Number]

MFCD09842757
[MOL File]

544461-38-3.mol
[Molecular Weight]

806.703
Chemical PropertiesBack Directory
[form ]

Powder
[color ]

yellow-brown
[Sensitive ]

air sensitive, light sensitive
Questions And AnswerBack Directory
[Reaction]

  1. Ligand for enantioselective Pd-catalyzed hydrogenation of enesulfonamides [5] and cyclic Nsulfonylimines.
  2. Enantioselective, asymmetric organocatalyst for cycloaddition of allenoates to C60 fullerene (conversion >90%, ee up to 90%)
  3. Ligand for Iridium-mediated direct asymmetric reductive amination of acetophenone with phenylhydrazide (conversion >99%; yield >94%; ee >94%)
  4. Ligand used for the palladium-catalyzed, asymmetric, decarboxylative generation and asymmetric allylation of α-imino anions.
  5. Ligand used in iridium-catalyzed, asymmetric hydrogenation of 6-substituted 3-hydroxypyridinium salts to trans 6-substituted piperidin-3-ols with high enantioselectivities(up to 95% ee).
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