
TY  - JOUR
A1  - Black, DS 
A1  - Keller, PA 
A1  - Kumar, N 
T1  - Nitrones and Oxaziridines. XLVI. Formation of Pyrrolo[3,2,1-<I>ij</I>]Quinolines by Intramolecular Nitrone Cycloaddition
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1993
VL  - 46
IS  - 6
SP  - 843
EP  - 862
KW  - 
UR  - https://doi.org/10.1071/CH9930843 
N2  - Intramolecular  1,3-dipolar cycloaddition occurs between nitrones derived from indole-7-carbaldehydes and adjacent allylic  substituents on the indole nitrogen atoms. The resulting pyrroloquinoline derivatives (4a-i) have been characterized fully. A range of other potential precursors to cycloaddition reactions have been synthesized, but cyclization sequences have not been completed. 
ER  -

