| Identification | Back Directory | [Name]
(R)-(6,6'-Dimethoxybiphenyl-2,2'-diyl)bis[bis(3,5-di-tert-butyl-4-methoxypheny | [CAS]
352655-61-9 | [Synonyms]
SL-A109-1
(R)-3,5-t-Bu-4-MeO-MeOBIPHEP
(R)-(6,6'-Dimethoxybiphenyl-2,2'-diyl)bis[bis(3,5-di-tert-butyl-4-methoxypheny
(R)-(6,6μ-Dimethoxybiphenyl-2,2μ-diyl)bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine]
(S)-(6,6μ-Dimethoxybiphenyl-2,2μ-diyl)bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphine]
(R)-(-)-2,2'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl
(R)-(-)-2,2'-Bis[di(3,5-di-t-butyl-4-methoxyphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl,min.97%
(R)-(-)-2,2''-BIS[DI(3,5-DI-T-BUTYL-4-METHOXYPHENYL)PHOSPHINO]-6,6''-DIMETHOXY-1,1''-BIPHENYL, MIN. 97%
(R)-(-)-2,2'-Bis[di-(3,5-di-t-butyl-4-methoxy- phenyl)phosphino]-(diphenylphosphino)-6,6'- dimethoxy-1,1'-biphenyl
(R)-(-)-2,2'-Bis[di-(3,5-di-tert-butyl-4-methoxy-phenyl)phosphino]-(diphenylphosphino)-6,6'-dimethoxy-1,1'-biphenyl
(R)-(6,6'-DiMethoxybiphenyl-2,2'-diyl)bis[bis(3,5-di-tert-butyl-4-Methoxyphenyl)phosphine] >=97%, optical purity ee: >=99%
(S)-3,5-t-Bu-4-MeO-MeOBIPHEP, SL-A109-2, (S)-[6,6μ-Dimethoxy(1,1μ-biphenyl)-2,2μ-diyl]bis{bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]phosphine}
(R)-3,5-t-Bu-4-MeO-MeOBIPHEP, SL-A109-1, (R)-[6,6μ-Dimethoxy(1,1μ-biphenyl)-2,2μ-diyl]bis{bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]phosphine} | [Molecular Formula]
C74H104O6P2 | [MDL Number]
MFCD09265029 | [MOL File]
352655-61-9.mol | [Molecular Weight]
1151.58 |
| Hazard Information | Back Directory | [Chemical Properties]
Off-white powder | [Uses]
Atropisomeric MeOBIPHEP ligands
- Asymmetrical conjugate addition of arylboronic acids to maleimides and enones catalyzed by rhodium complexes
- Intramolecular ketone hydroacylation
- Desymmetrization through enantioselective C-C bond activation and ring expansion of allenyl cyclobutanols
- Hydroamination of bicyclic alkenes and dienes with anilines
- 1,4-addition/asymmetric protonation of amino acrylates
| [General Description]
sold in collaboration with Solvias AG |
| Questions And Answer | Back Directory | [Reaction]
- Rh-catalyzed reductive coupling of acetylene to aldehydes and ketones.
- Pt-catalyzed intramolecular hydroarylation of unactivated alkenes with indoles.
- Enantioselective C-C bond activation of allenyl cyclobutanes.
- Enantioselective ring-opening of rac-ethynyl epoxides.
- Enantioselective Au-catalyzed allylic alkylation of indoles with alcohols.
- Enantioselective Rh-catalyzed conjugate alkynylation with TMS-acetylene.
- Enantioselective Rh-catalyzed [3+2] annulation of aromatic ketimines.
- Asymmetric Rh-catalyzed Pausan-Khand reaction.
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Energy Chemical
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Sigma-Aldrich
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