Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C28H28P2 |
| Molecular Weight | 426.4694 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H]([C@H](C)P(C1=CC=CC=C1)C2=CC=CC=C2)P(C3=CC=CC=C3)C4=CC=CC=C4
InChI
InChIKey=FWXAUDSWDBGCMN-ZEQRLZLVSA-N
InChI=1S/C28H28P2/c1-23(29(25-15-7-3-8-16-25)26-17-9-4-10-18-26)24(2)30(27-19-11-5-12-20-27)28-21-13-6-14-22-28/h3-24H,1-2H3/t23-,24-/m0/s1
| Molecular Formula | C28H28P2 |
| Molecular Weight | 426.4694 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Enantioselective synthesis of chiral sulfones by Rh-catalyzed asymmetric addition of boronic acids to alpha,beta-unsaturated 2-pyridyl sulfones. | 2007-12-21 |
|
| Stereoselective Rh-catalyzed hydrogenation of cyclobutyl chiral enamides: double stereodifferentiation vs catalyst-controlled diastereoselection. | 2004-11-12 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:01:32 GMT 2025
by
admin
on
Mon Mar 31 22:01:32 GMT 2025
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| Record UNII |
6QR78GZL9B
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| Record Status |
Validated (UNII)
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| Record Version |
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64896-28-2
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6QR78GZL9B
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m3333
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DTXSID60435814
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10113249
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