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Sku SC07-0307_1_G
US-Strem
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Product Information

Product Name
(-)-2,6-Bis(4S)-4-(i-propyl)-2-oxazolin-2-ylpyridine, 98+% (S)-(i-Pr)-pybox
Brand Name
US-Strem
Product Number
07-0307
CAS
118949-61-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
688211
IUPAC Name
(4S)-4-propan-2-yl-2-6-(4S)-4-propan-2-yl-4,5-dihydro-1,3-oxazol-2-yl-2-pyridinyl-4,5-dihydro-1,3-oxazole
InChI Key
CSGQGLBCAHGJDR-HUUCEWRRSA-N
SMILES
CC(C)C@H1COC(=N1)C2=NC(=CC=C2)C3=NC@H(CO3)C(C)C

Description

Technical Notes:
1. Ligand used in the dual-catalyst system for highly enantioselective conjugate cyanation of unsaturated imides.
2.Ligand for cross-coupling reactions of iodoalkanes with alkyI zinc halides.
3.L igand for asymmetric 1 , 4-addition reactions of 1,3-dicarbonyl compounds to nitroalkenes .
4.L igand for asymmetric allylation of alde hydes with b-carbonyl allylstannanes.
5.L igand used in the enantioselective Negishi reaction of racemic secondary benzylic halides. L igand for osmium catalyzed enantioselective transfer hydrogenation.
References:
1. J. Am. Chem. Soc., 2004, 126, 9928.
2.Angew. Chem. Int. Ed., 2007, 46, 87 90.
3.Angew. Chem. Int. Ed., 2009, 48, 91 1 7. 4.J. Organomet. Chem, 2010, 695, 128.
5. J. Am. Chem. Soc. 2005, 127, 10482. Inorg. Chem.2013, 52, 6193.

References Data Source From Pubchem

Difluoroalkylation of Alkyl Nucleophiles with Difluoroalkyl Electrophiles

Publication Name: Science of Synthesis
Publication Date: 2024

C–H Bond Functionalization of Amines: A Graphical Overview of Diverse Methods

Publication Name: SynOpen (2017)
Publication Date: 2021-07
DOI: 10.1055/s-0040-1706051

Enantioselective Cycloaddition Reactions

Publication Name: Science of Synthesis
Publication Date: 2021

Enantioselective Michael Reactions

Publication Name: Science of Synthesis
Publication Date: 2021

Amination and Related Processes

Publication Name: Science of Synthesis
Publication Date: 2021