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| (S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHEPTA[2,1-A:3,4-A']DINAPHTHALEN-4-YL)BIS[(1R)-1-PHENYLETHYL]AMINE,DICHLOROMETHANE ADDUCT Basic information | Reactions |
Product Name: | (S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHEPTA[2,1-A:3,4-A']DINAPHTHALEN-4-YL)BIS[(1R)-1-PHENYLETHYL]AMINE,DICHLOROMETHANE ADDUCT | Synonyms: | (S,R,R)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHE;3,4-a']dinaphthalen-4-yl)bis[(1R)-1-phenylethyl]amine,dichloromethaneadduct,min.95%;(+)-N,N-Bis[(1R)-1-phenylethyl]-dinaphtho[2,1-d:1μ,2μ-f][1,3,2]dioxaphosphepin-4-amine, (11bS);(S)-(+)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a:3,4-a']dinaphthalen-4-yl)bis[(1R)-1-phenylethyl]amine, dichloromethane adduct, min. 95%;(S)-(+)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a3,4-a']dinaphthalen-4-yl)bis[(1R)-1-phenylethyl]amine, dichloromethane adduct;(S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHEPTA[2,1-A:3,4-A']DINAPHTHALEN-4-YL)BIS[(1R)-1-PHENYLETHYL]AMINE,DICHLOROMETHANE ADDUCT;(R)-2,2-Binaphthoyl-(S,S)-di(1-phenylethyl)aminoylphosphine;(S,R,R)-(+)-(3,5-Dioxa-4-phosphacyclohepta[2,1-a | CAS: | 415918-91-1 | MF: | C36H30NO2P | MW: | 539.61 | EINECS: | | Product Categories: | Chiral Phosphine;CPN | Mol File: | 415918-91-1.mol | |
| (S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHEPTA[2,1-A:3,4-A']DINAPHTHALEN-4-YL)BIS[(1R)-1-PHENYLETHYL]AMINE,DICHLOROMETHANE ADDUCT Chemical Properties |
Melting point | 102-103 °C | Boiling point | 710.7±63.0 °C(Predicted) | alpha | +427° (c 0.83, CHCl3) | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | pka | -0.57±0.20(Predicted) | form | Powder | color | white | Sensitive | moisture sensitive | CAS DataBase Reference | 415918-91-1 |
| (S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHEPTA[2,1-A:3,4-A']DINAPHTHALEN-4-YL)BIS[(1R)-1-PHENYLETHYL]AMINE,DICHLOROMETHANE ADDUCT Usage And Synthesis |
Reactions |
- A ligand for asymmetric conjugate addition of dialkyl zinc reagents to activated olefins.
- Ligand used in the iridium-catalyzed, enantioselective addition of nucleophiles to achiral
- allylic esters.
- Asymmetric hydrogenation.
- Ir-catalyzed regio- and enantioselective Friedel-Crafts allylic alkylation of indoles.
- Asymmetric hydrovinylation.
- Used in 1,3-dipolar cycloaddition reactions of azomethine ylides and alkenes,9a and
- Rh-catalyzed [5+2] cycloaddition of alkyne-vinyl-cyclopropanes.9b
- Palladium-catalyzed enantioselective de-epimerization in catalytic asymmetric allylic alkylation.
- Palladium-catalyzed enantioselective diamination of alkyl dienes.
| Uses | (R,R,R)-(3,5-Dioxa-4-phosphacyclohepta[2,1-a:3,4-a'']dinaphthalen-4-yl)bis(1-phenylethyl)amine (CAS# 415918-91-1) is an organic catalyst used in the stereoselective preparation of homoallylic nitriles. |
| (S)-(+)-(3,5-DIOXA-4-PHOSPHA-CYCLOHEPTA[2,1-A:3,4-A']DINAPHTHALEN-4-YL)BIS[(1R)-1-PHENYLETHYL]AMINE,DICHLOROMETHANE ADDUCT Preparation Products And Raw materials |
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