Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C20H27P |
| Molecular Weight | 298.4021 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(C)P(C1=C(C=CC=C1)C2=CC=CC=C2)C(C)(C)C
InChI
InChIKey=CNXMDTWQWLGCPE-UHFFFAOYSA-N
InChI=1S/C20H27P/c1-19(2,3)21(20(4,5)6)18-15-11-10-14-17(18)16-12-8-7-9-13-16/h7-15H,1-6H3
| Molecular Formula | C20H27P |
| Molecular Weight | 298.4021 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Influence of biaryl phosphine structure on C-N and C-C bond formation. | 2009-09-02 |
|
| FeCl3-catalyzed 1,2-addition reactions of aryl aldehydes with arylboronic acids. | 2009-01-15 |
|
| Addition of alkynes to aldehydes and activated ketones catalyzed by rhodium-phosphine complexes. | 2007-12-07 |
|
| Synthesis of gerfelin and related analogous compounds. | 2006-10 |
|
| Rhodium-catalyzed addition of alkynes to activated ketones and aldehydes. | 2006-01-05 |
|
| Stereoselective palladium-catalyzed O-glycosylation using glycals. | 2004-02-11 |
|
| Synthesis of substituted oxindoles from alpha-chloroacetanilides via palladium-catalyzed C[bond]H functionalization. | 2003-10-08 |
|
| A mild and efficient method for the stereoselective formation of C-O bonds: palladium-catalyzed allylic etherification using zinc(II) alkoxides. | 2002-11-28 |
|
| Improved synthesis of aryltriethoxysilanes via palladium(0)-catalyzed silylation of aryl iodides and bromides with triethoxysilane. | 2001-11-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:42:21 GMT 2025
by
admin
on
Mon Mar 31 22:42:21 GMT 2025
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| Record UNII |
5Y743P380H
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| Record Status |
Validated (UNII)
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| Record Version |
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5Y743P380H
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2734215
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m2739
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224311-51-7
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