Unknown

Dataset Information

0

Nitropyridines as 2π-Partners in 1,3-Dipolar Cycloadditions with N-Methyl Azomethine Ylide: An Easy Access to Condensed Pyrrolines.


ABSTRACT: 1,3-Dipolar cycloaddition reactions of 2-substituted 5-R-3-nitropyridines and isomeric 3-R-5-nitropyridines with N-methyl azomethine ylide were studied. The effect of the substituent at positions 2 and 5 of the pyridine ring on the possibility of the [3+2]-cycloaddition process was revealed. A number of new derivatives of pyrroline and pyrrolidine condensed with a pyridine ring were synthesized.

SUBMITTER: Bastrakov MA 

PROVIDER: S-EPMC8471275 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC4004623 | biostudies-other
| S-EPMC8456807 | biostudies-literature
| S-EPMC7540365 | biostudies-literature
| S-EPMC4142980 | biostudies-literature
| S-EPMC7075354 | biostudies-literature
| S-EPMC3943969 | biostudies-literature
| S-EPMC4113408 | biostudies-literature
| S-EPMC5141247 | biostudies-literature
| S-EPMC3876797 | biostudies-literature
| S-EPMC10809861 | biostudies-literature