Brief introduction of 132098-59-0

From this literature《Enantiotopic Differentiation of pro-R or pro-S Chlorides in (Dichloromethyl)borates by Chiral Lewis Acids: Enantioselective Synthesis of (α-Chloroalkyl)boronates》,we know some information about this compound(132098-59-0)Computed Properties of C19H18N2O2, but this is not all information, there are many literatures related to this compound(132098-59-0).

Computed Properties of C19H18N2O2. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)methane, is researched, Molecular C19H18N2O2, CAS is 132098-59-0, about Enantiotopic Differentiation of pro-R or pro-S Chlorides in (Dichloromethyl)borates by Chiral Lewis Acids: Enantioselective Synthesis of (α-Chloroalkyl)boronates. Author is Jadhav, Prabhakar K.; Man, Hon-Wah.

The 1,2-migration reaction of an alkyl group in borate complexes, I (e.g. R = Bu), derived from dichloromethyl pinacol boronates and alkyllithium was catalyzed by chiral Lewis acids capable of enantiotopic differentiation of Pro (R) or Pro (S) chloride groups on an sp3 C center. It takes place with an enantiomeric ratio of 94:6 to provide α-chloroalkylboronates, II, in 70-75% chem. yields. Chiral Lewis acids examined in this study were prepared in situ from ZnEt2, Yb(OTf)3, Cu(OTf)2, Zn(OTf)2 or Lu(OTf)3 and chiral ligands including amino alcs. and bisoxazolines. Highest enantioselectivity (88% ee) was observed with the chiral Lewis acid derived from Yb(OTf)3 and bisoxazoline III. This is the 1st example of a chiral Lewis acid catalyzed enantioselective 1,2-migration reaction of dichloromethylborate complexes.

From this literature《Enantiotopic Differentiation of pro-R or pro-S Chlorides in (Dichloromethyl)borates by Chiral Lewis Acids: Enantioselective Synthesis of (α-Chloroalkyl)boronates》,we know some information about this compound(132098-59-0)Computed Properties of C19H18N2O2, but this is not all information, there are many literatures related to this compound(132098-59-0).

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles