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Home  > 1,2-Bis((2S,5S)-2,5-diisopropylphospholano)benzene(cyclooctadiene)rhodium(I) tetrafluoroborate

AA00616

1000393-36-1 | 1,2-Bis((2S,5S)-2,5-diisopropylphospholano)benzene(cyclooctadiene)rhodium(I) tetrafluoroborate

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Description
Catalog Number: AA00616
Chemical Name: 1,2-Bis((2S,5S)-2,5-diisopropylphospholano)benzene(cyclooctadiene)rhodium(I) tetrafluoroborate
CAS Number: 1000393-36-1
Molecular Formula: C34H56BF4P2Rh
Molecular Weight: 716.4661
MDL Number: MFCD07369040
SMILES: [F-][B+3]([F-])([F-])[F-].CC([C@@H]1CC[C@H](P21c1ccccc1P1([Rh+]3452[CH]2=[CH]5CC[CH]3=[CH]4CC2)[C@@H](CC[C@H]1C(C)C)C(C)C)C(C)C)C

 

Upstream Synthesis Route
  • 1,2-Bis[(2S,5S)-2,5-diisopropylphospholano]benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, commonly known as Rh-Diene, is a versatile catalyst frequently employed in chemical synthesis. This catalyst plays a crucial role in promoting various types of organic transformations, particularly in the realm of asymmetric hydrogenation reactions. In chemical synthesis, Rh-Diene is widely utilized for its exceptional ability to catalyze the hydrogenation of a range of unsaturated substrates with high efficiency and selectivity. This catalyst is especially valued for enabling enantioselective hydrogenation reactions, providing access to chiral molecules that are vital in the pharmaceutical, agrochemical, and material science industries.Moreover, Rh-Diene exhibits excellent reactivity towards a diverse array of functional groups, allowing chemists to carry out complex transformations with exquisite control over stereochemistry. Its unique structural features, including the chiral ligands and the rhodium center, contribute to its remarkable catalytic performance and make it a prized tool in the synthetic chemist's arsenal.Overall, the application of 1,2-Bis[(2S,5S)-2,5-diisopropylphospholano]benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate in chemical synthesis underscores its pivotal role in facilitating the creation of valuable organic molecules with high levels of selectivity and efficiency.
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