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(4S,4'S)-2,2'-(1,3-Bis[4-(t-butyl)phenyl)propane-2,2-diyl]bis(4-phenyl-4,5-dihydrooxazole) (S)-BTBBPh-SaBOX|07-1235|1428328-51-1

(4S,4'S)-2,2'-(1,3-Bis[4-(t-butyl)phenyl)propane-2,2-diyl]bis(4-phenyl-4,5-dihydrooxazole) (S)-BTBBPh-SaBOX

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Sku SC07-1235_250_MG
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Product Information

Product Name
(4S,4'S)-2,2'-(1,3-Bis4-(t-butyl)phenyl)propane-2,2-diylbis(4-phenyl-4,5-dihydrooxazole) (S)-BTBBPh-SaBOX
Brand Name
US-Strem
Product Number
07-1235
CAS
1428328-51-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
71608540
IUPAC Name
(4S)-2-1,3-bis(4-tert-butylphenyl)-2-(4S)-4-phenyl-4,5-dihydro-1,3-oxazol-2-ylpropan-2-yl-4-phenyl-4,5-dihydro-1,3-oxazole
InChI Key
CONTYZSPSXHNNJ-LQFQNGICSA-N
SMILES
CC(C)(C)C1=CC=C(C=C1)CC(CC2=CC=C(C=C2)C(C)(C)C)(C3=NC@H(CO3)C4=CC=CC=C4)C5=NC@H(CO5)C6=CC=CC=C6

Description

Technical Note:
1. A chiral cage like copper (I) catalyst for the highly enantioselective synthesis of 1.1- cyclopropane diesters. 2.Direct catalytic asymmetric synthesis of ß-hydroxy acids from malonic acid.
3. Asymmetric intramolecular desymmetrization of meso-a,a -diazido alcohols with aryldiazoacetates.
4. Catalytic asymmetric 3+ 1-cycloaddition re action of ylides with electrophilic metallo-enolcarbene
intermediates.
References:
1.Angew. Chem. Int. Ed., 2012, 51, 11620. 2. 2.Org. Lett., 2015, 17, 5962.
3.Org. L ett., 2016, 18, 1984.
4. Angew. Chem. int. Ed., 2017, 56, 7479.

References Data Source From Pubchem

Regio- and Enantioselective Hydrofluorination
Publication Name: Science of Synthesis
Publication Date: 2025

High Stereocontrol in the Preparation of Silyl-Protected γ-Substituted Enoldiazoacetates
Publication Name: Synlett
Publication Date: 2019-06-26
DOI: 10.1055/s-0037-1611865

Copper-Catalyzed Enantioselective [3+1] Cycloaddition Reaction
Publication Name: Synfacts
Publication Date: 2017-07-18
DOI: 10.1055/s-0036-1590658

Catalytic Asymmetric Synthesis of β-Hydroxy Acids from Malonic Acid
Publication Name: Synfacts
Publication Date: 2016-01-19
DOI: 10.1055/s-0035-1561195