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| (R)-(-)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BINAPHTHYL-2,2'-DIYL HYDROGENPHOSPHATE, 95% Basic information | Reaction |
Product Name: | (R)-(-)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BINAPHTHYL-2,2'-DIYL HYDROGENPHOSPHATE, 95% | Synonyms: | (R)-(-)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BINAPHTHYL-2,2'-DIYL HYDROGENPHOSPHATE, 95%;MacMillan TiPSY catalyst, (11bR)-4-Hydroxy-2,6-bis(triphenylsilyl)dinaphtho-[2,1-d:1μ,2μf]-1,3,2-dioxaphosphepin 4-oxide;(S)-3,3μ-Bis(triphenylsilyl)-1,1μ-binaphthyl-2,2μ-diyl hydrogenphosphate;MacMillan TiPSY catalyst, (11bS)-4-Hydroxy-2,6-bis(triphenylsilyl)dinaphtho-[2,1-d1μ,2μf]-[1,3,2]-dioxaphosphepin 4-oxide;(R)-(-)-3,3'Bis(triphenylsilyl)-1,1'binaphthyl-2,2'diyl hydrogenphosphaste;(R)-(-)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BINAPHTHYL-2,2'-DIYLHYDROGENPHOSPHATE,95%;(R)-(-)-3,3'-Bis(triphenylsilyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate 96%;Carreira SALDIPAC Ligand | CAS: | 791616-55-2 | MF: | C56H41O4PSi2 | MW: | 865.07 | EINECS: | | Product Categories: | | Mol File: | 791616-55-2.mol | |
| (R)-(-)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BINAPHTHYL-2,2'-DIYL HYDROGENPHOSPHATE, 95% Chemical Properties |
Melting point | 329-335 °C | alpha | -197° (c=1, CHCl3) | density | 1.32±0.1 g/cm3(Predicted) | storage temp. | Sealed in dry,Room Temperature | pka | 1.17±0.20(Predicted) | form | Powder | color | white to light-yellow | optical activity | [α]22/D -197°, c = 1 in chloroform |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36/37 | WGK Germany | 3 | HS Code | 29319090 |
| (R)-(-)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BINAPHTHYL-2,2'-DIYL HYDROGENPHOSPHATE, 95% Usage And Synthesis |
Reaction |
- A chiral phosphoric acid catalyst providing a convenient strategy for the enantioselective construction of protected primary amines and a highly stereoselective method for the reductive amination of heterocyclic amines.
- Chiral phosphoric acid used for the enantioselective Biginelli and Biginelli-like reactions.
- Chiral phosphoric acid organocatalyst used in the asymmetric, three-component Povarov reaction involving 2-hydroxystyrenes. An efficient method to access structurally diverse cis-disubstituted tetrahydroquinolines in high stereoselectivities of up to >99:1 dr and 97% ee.
- A gold/chiral phosphoric acid catalyst used for the highly stereoselective, three-component reaction of salicylaldehydes, anilines, and alkynols to give aromatic spiroacetals in high yields and stereoselectivities.
- The first highly enantioselective catalytic protocol for the reductive coupling of ketones and hydrozones.
- Reagent-controlled regioselectivity enabled by dual activation.
| Chemical Properties | Solid | Uses | Organocatalyst for the first enatioselective organocatalytic reductive amination reaction. |
| (R)-(-)-3,3'-BIS(TRIPHENYLSILYL)-1,1'-BINAPHTHYL-2,2'-DIYL HYDROGENPHOSPHATE, 95% Preparation Products And Raw materials |
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