
TY  - JOUR
A1  - Black, DSC 
A1  - Rothnie, NE 
A1  - Wong, LCH 
T1  - Metal template reactions. XX. Macrocyclic metal complexes derived from 4,6-Dimethoxy-3-methylindole-2,7-dicarbaldehyde and some primary diamines with additional nitrogen donor atoms
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1983
VL  - 36
IS  - 12
SP  - 2407
EP  - 2412
KW  - 
UR  - https://doi.org/10.1071/CH9832407 
N2  - 4,6-Dimethoxy-3-methylindole-2,7-dicarbaldehyde (6) has been prepared by the formylation of 4,6-dimethoxy-3-methylindole (5)itself prepared by the hydride reduction of the oxoindole (4). Macrocyclic nickel(II) and copper(II) complexes (8), (10) and (12) have been prepared from the dialdehyde (6), the appropriate metal(II) acetate and the primary diamines 2,2'-iminobisaniline (7), 2-amino-N-(2'-aminophenyl)benzamide (9) and 2-amino-N-(2'-aminobenzoyl)benzamide (11) respectively. 
ER  -

