Catalysts Ligands Chiral Phosphine Ligands BIDIME-BIBOP 2,2',3,3'-Tetrahydro-4,4'-Bibenzo[D][1,3]Oxaphosphole

2,2',3,3'-Tetrahydro-4,4'-Bibenzo[D][1,3]Oxaphosphole

Aromatic Substitution: The compound has aromatic rings in its structure. Aromatic compounds can undergo electrophilic aromatic substitution reactions, where an electrophile replaces a hydrogen atom on the aromatic ring. Common electrophiles include halogens (e.g., chlorine or bromine) or other electron-deficient species. Nucleophilic Substitution: Depending on the functional groups present in the molecule, it might be susceptible to nucleophilic substitution reactions. For instance, if it has halogen substituents (e.g., chloro or bromo groups), these can be replaced by nucleophiles like hydroxide ions or amines. Hydrolysis: If the compound contains ester groups, it can undergo hydrolysis reactions in the presence of water or acidic or basic conditions, breaking the ester bonds. Ring Opening/Closure: The compound's unique structure suggests the possibility of ring-opening or ring-closing reactions. These reactions can involve breaking or forming bonds within the molecule. Photochemical Reactions: Some organic compounds are sensitive to light and can undergo photochemical reactions when exposed to UV or visible light. Metal-Catalyzed Reactions: Transition metals can catalyze various reactions, including cross-coupling reactions or hydrogenation reactions, depending on the functional groups present. Polymerization: If the compound has reactive groups, it might participate in polymerization reactions, forming larger, chain-like molecules. Lewis Acid/Base Reactions: The phosphorus atom in the compound might act as a Lewis acid, accepting electron pairs from Lewis bases, leading to various reactions.

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2,2',3,3'-Tetrahydro-4,4'-Bibenzo[D][1,3]Oxaphosphole
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(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-diisopropyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

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A11751252207601-12-397% 99%ee

(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-diisopropyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

$171.00/50mg

Detail
(2R,2'R,3R,3'R)-3,3'-Di-tert-butyl-2,2'-diethyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

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A12076492634687-61-797+%

(2R,2'R,3R,3'R)-3,3'-Di-tert-butyl-2,2'-diethyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

$191.00/50mg

Detail
(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-diethyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

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A12076212415751-83-497% 99%ee

(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-diethyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

$349.00/25mg

Detail
(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-dimethyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

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A11751242207601-10-195% 99%ee

(2S,2'S,3S,3'S)-3,3'-Di-tert-butyl-2,2'-dimethyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

$183.00/50mg

Detail
(3S,3'S)-3,3'-Di-tert-butyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

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A11751222207601-04-397%

(3S,3'S)-3,3'-Di-tert-butyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

$629.00/250mg

Detail
(2R,2'R,3R,3'R)-3,3'-Di-tert-butyl-2,2'-diisopropyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

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A11751272214207-75-597%

(2R,2'R,3R,3'R)-3,3'-Di-tert-butyl-2,2'-diisopropyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

$280.00/100mg

Detail
(3R,3'R)-3,3'-Di-tert-butyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

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A11751232214207-73-397%

(3R,3'R)-3,3'-Di-tert-butyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

$220.00/50mg

Detail
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