N-Phenyl-2-(di-t-butylphosphino)indol, min. 98% [cataCXium? PIntB]|15-3550|740815-37-6

N-Phenyl-2-(di-t-butylphosphino)indol, min. 98% [cataCXium? PIntB]

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Sku SC15-3550_2_G
US-Strem
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Product Information

Product Name
N-Phenyl-2-(di-t-butylphosphino)indol, min. 98% cataCXium? PIntB
Brand Name
US-Strem
Product Number
15-3550
CAS
740815-37-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11175133
IUPAC Name
ditert-butyl-(1-phenylindol-2-yl)phosphane
InChI Key
HDZRDZCQFYUOHE-UHFFFAOYSA-N
SMILES
CC(C)(C)P(C1=CC2=CC=CC=C2N1C3=CC=CC=C3)C(C)(C)C

Application

Technical Notes:
1. Useful ligand for the Pd-catalyzed amination reaction.
2.Ligand used for the F d-catalyzed arylation of phenols.
3.UsefuI ligand for the Suzuki-Miyaura coupling.
4.L igand used for the Sonagashira reaction of aryl bromides.
References:
1.Chem. EurJ. 2004, 10, 2983
2.Tetrahedron L ett., 2005, 46, 3237.
3.J.Org. Chem., 2009, 74, 3948.
4.Chem. Sus. Chem., 2008, 1, 91.

References

Palladium-Mediated Coupling of Halobenzo[b]thiophenes
Publication Name: Science of Synthesis
Publication Date: 2020

Iron-Catalyzed Carbonylation as a Key Step in the Short and Efficient Syntheses of Himanimide A and B
Publication Name: Chemistry – An Asian Journal
Publication Date: 2010-07-23
DOI: 10.1002/asia.201000384

A Rapid and Efficient Sonogashira Protocol and Improved Synthesis of Free Fatty Acid 1 (FFA1) Receptor Agonists
Publication Name: The Journal of Organic Chemistry
Publication Date: 2010-01-25
DOI: 10.1021/jo902533p

Palladium-Promoted Cross-Coupling Reactions
Publication Name: Science of Synthesis
Publication Date: 2009

Amination of Aryl and Hetaryl Halides or Trifluoromethanesulfonates
Publication Name: Science of Synthesis
Publication Date: 2009