
TY  - JOUR
A1  - Gable, RW 
A1  - Martin, RL 
A1  - Rizzacasa, MA 
T1  - A Synthetic Approach to (+)-Dioncophylline C
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1995
VL  - 48
IS  - 12
SP  - 2013
EP  - 2021
KW  - 
UR  - https://doi.org/10.1071/CH9952013 
N2  - In a synthetic approach to (+)-dioncophylline C (1), a coupling between the chiral oxazoline (3) and the Grignard reagent obtained from bromide (4) gave the major biaryl (5) and the minor biaryl (12) in good yield and high diastereoselectivity (yield 70%; ratio 91:9). The stereochemistry of the major biaryl (5) was confirmed by X-ray structure analysis of the derived crystalline iodide salt (13). 
ER  -

