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- A multicomponent pathway-inspired regioselective synthesis of 2,3,4-trisubstituted 1H-pyrroles via [3+2] cycloaddition reaction. Hanuman P. Kalmode, Kamlesh S. Vadagaonkar, Kaliyappan Murugan, Atul C. Chaskar
, New J. Chem.
, 2015
, 39
, 4631
- An isoxazole strategy for the synthesis of alkyl 5-amino-4-cyano-1H-pyrrole-2-carboxylates – versatile building blocks for assembling pyrrolo-fused heterocycles. Anastasiya V. Agafonova, Liya D. Funt, Mikhail S. Novikov, Alexander F. Khlebnikov
, Org. Biomol. Chem.
, 2021
, 19
, 1976
- Deep eutectic solvent: a simple, environmentally benign reaction media for regioselective synthesis of 2,3,4-trisubstituted 1H-pyrroles. Hanuman P. Kalmode, Kamlesh S. Vadagaonkar, Kaliyappan Murugan, Sattey Prakash, Atul C. Chaskar
, RSC Adv.
, 2015
, 5
, 35166
- Metal/organo relay catalysis in a one-pot synthesis of methyl 4-aminopyrrole-2-carboxylates from 5-methoxyisoxazoles and pyridinium ylides. Ekaterina E. Galenko, Olesya A. Tomashenko, Alexander F. Khlebnikov, Mikhail S. Novikov
, Org. Biomol. Chem.
, 2015
, 13
, 9825
- Stereochemical studies on porphyrin a: assignment of the absolute configuration of a model porphyrin by degradation. Alan R. Battersby, Kevin S. Cardwell, Finian J. Leeper
, J. Chem. Soc., Perkin Trans. 1
, 1986
, 1565
- Synthesis of a gable bis-porphyrin linked with a bicyclo[2.2.2]octadiene ring and its conversion into a conjugated planar bis-porphyrin. Satoshi Ito, Ken-ichi Nakamoto, Hidemitsu Uno, Takashi Murashima, Noboru Ono
, Chem. Commun.
, 2001
, 2696