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901417

Sigma-Aldrich

N-((1S,2S)-1-((R)-4-Isobutyl-4,5-dihydrooxazol-2-yl)-2-methylbutyl)acetamide

Synonym(s):

Chiral APAO ligand

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About This Item

Empirical Formula (Hill Notation):
C14H26N2O2
CAS Number:
2083655-63-2
Molecular Weight:
254.37
UNSPSC Code:
12352202

form

powder or crystals

reaction suitability

reagent type: catalyst
reagent type: ligand
reaction type: C-H Activation

storage temp.

−20°C

Application

Chiral bidentate ligand developed by Jin-Quan Yu.′s lab for enantioselective borylation of C(sp3)–H bonds. This acetyl-protected aminomethyl oxazoline (APAO) ligand was demonstrated to be compatible with carbocyclic substrates with both α-tertiary and α-quaternary carbon centres.

Other Notes

Pd(II)-Catalyzed Enantioselective C(sp3)–H Borylation.

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Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Jian He et al.
Journal of the American Chemical Society, 139(9), 3344-3347 (2017-02-18)
Pd(II)-catalyzed enantioselective borylation of C(sp

Related Content

Yu Group – Professor Product Portal

The Yu program centers around the discovery of catalytic carbon–carbon and carbon–heteroatom bond forming reactions based on C–H activation. Target transformations are selected to enable 1) the use of simple and abundant starting materials such as aliphatic acids, amines and alcohols, and 2) disconnections that drastically shorten the synthesis of a drug molecule or a major class of biologically active compounds.

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