One pot synthesis of pyridophenanthroline and pyrrolophenanthroline derivatives by regioselective reaction between 1,7-phenanthroline and dialkyl acetylenedicarboxylate: new fused heterocyclic compounds

Authors

MALEK TAHER MAGHSOODLOU
REZA HEYDARI
SAYYED MOSTAFA HABIBI KHORASSANI
BATOOL TAHAMI POUR
GHASEM MARANDI
FARHAD MAGHFURI

Abstract

1,7-Phenanthroline reacts with dialkyl acetylenedicarboxylate in a regioselective manner to give new macromolecules such as tetramethyl- 6aH-pyrido[1,2-i][1,7]phenanthroline-7,8,9,10-tetracarboxylate and trialkyl pyrrolo[1,2-i][1,7]phenanthroline-7,8,9-tricarboxylate derivatives.

DOI

10.3906/kim-0912-405

Keywords

1, 7-Phenanthroline, tetramethyl-6aH-pyrido[1, 2-i][1, 7] phenanthroline-7, 8, 9, 10-tetracarboxylate, trialkyl pyrrolo[1, 2-i] [1, 7]phenanthroline-7, 8, 9-tricarboxylate derivatives, regioselective cycloaddition reaction

First Page

405

Last Page

412

Recommended Citation

MAGHSOODLOU, M. T, HEYDARI, R, KHORASSANI, S. M, POUR, B. T, MARANDI, G, & MAGHFURI, F (2011). One pot synthesis of pyridophenanthroline and pyrrolophenanthroline derivatives by regioselective reaction between 1,7-phenanthroline and dialkyl acetylenedicarboxylate: new fused heterocyclic compounds. Turkish Journal of Chemistry 35 (3): 405-412. https://doi.org/10.3906/kim-0912-405