Coumarin heterocyclic derivatives: chemical synthesis and biological activity
FG Medina, JG Marrero, M Macías-Alonso… - Natural product …, 2015 - pubs.rsc.org
Coumarin heterocyclic derivatives: chemical synthesis and biological activity - Natural Product
Reports (RSC Publishing) DOI:10.1039/C4NP00162A Royal Society of Chemistry View PDF …
Reports (RSC Publishing) DOI:10.1039/C4NP00162A Royal Society of Chemistry View PDF …
Allenes and computational chemistry: from bonding situations to reaction mechanisms
E Soriano, I Fernández - Chemical Society Reviews, 2014 - pubs.rsc.org
The present review is focused on the application of computational/theoretical methods to the
wide and rich chemistry of allenes. Special emphasis is made on the interplay and synergy …
wide and rich chemistry of allenes. Special emphasis is made on the interplay and synergy …
Intramolecular Heterocyclization of O-Propargylated Aromatic Hydroxyaldehydes as an Expedient Route to Substituted Chromenopyridines under Metal-Free …
A concise and regioselective approach to the synthesis of chromenopyridine and
chromenopyridinone derivatives was developed. The synthetic strategy relies on the O …
chromenopyridinone derivatives was developed. The synthetic strategy relies on the O …
Synthesis of polysubstituted pyridines via a one-pot metal-free strategy
H Wei, Y Li, K Xiao, B Cheng, H Wang, L Hu… - Organic letters, 2015 - ACS Publications
An efficient strategy for the one-pot synthesis of polysubstituted pyridines via a cascade
reaction from aldehydes, phosphorus ylides, and propargyl azide is reported. The reaction …
reaction from aldehydes, phosphorus ylides, and propargyl azide is reported. The reaction …
N-Acyl pyrroles: chemoselective pyrrole dance vs. C–H functionalization/aroylation of toluenes
H Wang, J Mao, SJ Shuai, S Chen, D Zou… - Organic Chemistry …, 2021 - pubs.rsc.org
Chemoselectivity is one of the most challenging issues facing the chemical sciences. In this
study, the first highly chemoselective reactions of N-acylpyrroles via either an anionic Fries …
study, the first highly chemoselective reactions of N-acylpyrroles via either an anionic Fries …
Intramolecular Gold-Catalyzed and NaH-Supported Cyclization Reactions of N-Propargyl Indole Derivatives with Pyrazole and Pyrrole Rings: Synthesis of …
Gold-catalyzed and NaH-supported intramolecular cyclization of N-propargyl indole
derivatives with pyrazole and pyrrole units attached to indole is described. An efficient route …
derivatives with pyrazole and pyrrole units attached to indole is described. An efficient route …
Design of Pyrazolo-pyrrolo-pyrazines and Pyrazolo-pyrrolo-diazepines via AuCl3-Catalyzed and NaH-Supported Cyclization of N-Propargyl Pyrazoles
S Basceken, M Balci - The Journal of Organic Chemistry, 2015 - ACS Publications
A concise synthetic methodology for new heterocyclic scaffolds, such as pyrazolo-pyrrolo-
pyrazine and pyrazolo-pyrrolo-diazepine skeletons, was developed. The key features of this …
pyrazine and pyrazolo-pyrrolo-diazepine skeletons, was developed. The key features of this …
Gold-catalyzed oxime–oxime rearrangement
The gold-catalyzed reaction of pyrrole and indole oximes having a propargyl group attached
to the nitrogen atom was studied. The selective 6-endo-dig mode of cyclization was …
to the nitrogen atom was studied. The selective 6-endo-dig mode of cyclization was …
Cascade synthesis of indolizines and pyrrolo [1, 2-a] pyrazines from 2-formyl-1-propargylpyrroles
CH Escalante, FA Carmona-Hernández… - Organic & …, 2022 - pubs.rsc.org
A straightforward synthesis of indolizines and pyrrolo [1, 2-a] pyrazines was performed
through a cascade condensation/cyclization/aromatization reaction of substituted 2-formyl-N …
through a cascade condensation/cyclization/aromatization reaction of substituted 2-formyl-N …