675792
(S)-(−)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine
97%
Synonym(s):
(S)-P-Phos
About This Item
Recommended Products
Assay
97%
optical activity
[α]20/D -98°, c = 1 in chloroform
mp
261-265 °C
functional group
phosphine
SMILES string
COc1cc(P(c2ccccc2)c3ccccc3)c(c(OC)n1)-c4c(OC)nc(OC)cc4P(c5ccccc5)c6ccccc6
InChI
1S/C38H34N2O4P2/c1-41-33-25-31(45(27-17-9-5-10-18-27)28-19-11-6-12-20-28)35(37(39-33)43-3)36-32(26-34(42-2)40-38(36)44-4)46(29-21-13-7-14-22-29)30-23-15-8-16-24-30/h5-26H,1-4H3
InChI key
JZOSBBLJKXSBBN-UHFFFAOYSA-N
Application
- In the asymmetic hydrogenation reactions.
- For the preparation of chiral ketone functionalized polymers by copolymerization reaction.
- To synthesize chiral alkynes by asymmetric hydroalkynylation of nonpolar alkenes or norbornadienes using iridium catalyst.
- In the selective allylic alkylation of indoles using palladium catalyst.
Legal Information
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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Articles
P-Phos ligand family enhances catalysis, featuring atropisomeric biaryl bisphosphine with unique structural elements.
P-Phos ligand family enhances catalysis, featuring atropisomeric biaryl bisphosphine with unique structural elements.
P-Phos ligand family enhances catalysis, featuring atropisomeric biaryl bisphosphine with unique structural elements.
P-Phos ligand family enhances catalysis, featuring atropisomeric biaryl bisphosphine with unique structural elements.
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