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(4S,4'S,5R,5'R)-2,2'-Cyclopropylidenebis[4,5-dihydro-4,5-diphenyloxazole], 95%, (99% ee)|07-1412|229184-97-8

(4S,4'S,5R,5'R)-2,2'-Cyclopropylidenebis[4,5-dihydro-4,5-diphenyloxazole], 95%, (99% ee)

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Sku SC07-1412_50_MG
US-Strem
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Product Information

Product Name
(4S,4'S,5R,5'R)-2,2'-Cyclopropylidenebis4,5-dihydro-4,5-diphenyloxazole, 95%, (99% ee)
Brand Name
US-Strem
Product Number
07-1412
CAS
229184-97-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
58489047
IUPAC Name
(4S,5R)-2-1-(4S,5R)-4,5-diphenyl-4,5-dihydro-1,3-oxazol-2-ylcyclopropyl-4,5-diphenyl-4,5-dihydro-1,3-oxazole
InChI Key
UAXGHJCFHMQPBJ-VZNYXHRGSA-N
SMILES
C1CC1(C2=NC@H(C@H(O2)C3=CC=CC=C3)C4=CC=CC=C4)C5=NC@H(C@H(O5)C6=CC=CC=C6)C7=CC=CC=C7

Safety Information

Storage Condition
Store at 2-8℃

Description

Technical Notes：
1.Ligand for the catalytic enantioselective conjugate addition of 1 ,3-dicarbonyl compounds to nitroalkenes.
2.L igand for the Cu-catalyzed asymmetric annulation reactions of carbenes with 2-iminyl- or 2-acyl-substituted phenols .
References:
1.J. Am. Chem. Soc. 1999, 121, 10215.
2.J. Am. Chem. Soc. 2002, 124, 13097.
3.Angew. Chem. Int. Ed. 2019, 58, 13885.

References Data Source From Pubchem

Recent Advances in Synthetic Strategies to 2,3-Dihydrobenzofurans
Publication Name: Synthesis
Publication Date: 2020-03-16
DOI: 10.1055/s-0039-1690820