(S,S,S)-(+)-(3,5-Dioxa-4-phosphacyclohepta[2,1-a:3,4-a’]dinaphthalen-4-yl)bis(1-phenylethyl)amine
ALDRICH/665290 - 97%
Synonym: (+)-N,N-Bis[(1S)-1-phenylethyl]- dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin- 4-amine, (11bR)
CAS Number: 380230-02-4
Empirical Formula (Hill Notation): C36H30NO2P
Molecular Weight: 539.60
MDL Number: MFCD04117688
Linear Formula: C36H30NO2P
Product Type: Chemical
assay | 97% |
form | solid |
InChI | 1S/C36H30NO2P/c1-25(27-13 |
InChI key | LKZPDRCMCSBQFN-UIOOFZCWSA |
mp | 88-89 °C |
SMILES string | C[C@H](N([C@@H](C)c1ccccc |
Application: | DSM MonoPhos Family of Highly Efficient Privileged Ligands |
Application: | Chiral phosphoramidite ligand used in a highly enantioselective copper-catalyzed conjugate addition of diakylzincs to a variety of Michael acceptors. Also used in a palladium-catalyzed diethylzinc mediated umpolung allylation. |
Application: | The product may be used as a ligand in: • Iridium-catalyzed allylic etherification of acyclic, achiral allylic carbonates with potassium silanolates to form chiral allylic alcohols. • Palladium-catalyzed asymmetric allylic cyclisation of N-tosyl and N-benzyl carbonates to form the corresponding pyrrolidine and piperidine derivatives, respectively. • Intramolecular iridium-catalyzed allylic cyclizationof (E)-allylic methyl carbonates to form 2,5-trans/cis pyrrolidine derivatives. |
Features and Benefits: | Advantages of the MonoPhos® ligands: • Superior enantiocontrol in numerous transformations • High activities at low catalyst loadings • Hydrogenations under low-pressure conditions |
Legal Information: | MonoPhos is a registered trademark of DSM IP Assets B.V. |
Legal Information: | Sold under license from DSM for research purposes only. |
Packaging: | 100, 500 mg in glass insert |
Packaging: | 2 g in glass bottle |
RIDADR | NONH for all modes of transport |
WGK Germany | WGK 3 |
Flash Point(F) | Not applicable |
Flash Point(C) | Not applicable |
Purity | 97% |
mp | 88-89 °C |
UNSPSC | 12352005 |