Nomenclature
CAS number: 159752-39-3
[2-[(1
R)-1-Methoxyethyl]phenyl]boronic acid.
C
9H
13BO
3; mol wt 180.01.
C 60.05%, H 7.28%, B 6.01%, O 26.66%.
Description and references
Synthesis of (+)-form and use: K. Burgess,
A. M. Porte, Angew. Chem. Int. Ed. 33, 1182 (1994). Chemoenzymatic stereosynthesis of both
enantiomers and use: S. M. Resnick et al., J. Org. Chem. 60, 3546 (1995).
Properties
White solid from n-hexane, mp 72-74°. [Ga]D25 +27 (c = 0.5 in CH2Cl2) (Burgess); [α]D +27.2° (c = 4.6 in CH2Cl2) (Resnick).Derivative
()-S-Form.
Nomenclature
CAS number: 166191-23-7
Properties
[α]D 28.7° (c = 2.3 in CH2Cl2).Use
NMR shift reagent for enantiomeric assay of diols.