Transition Metal-Mediated Synthesis of Monocyclic Aromatic Heterocycles | Chemical Reviews ACS ACS Publications C&EN CAS Find my institution Log In Chemical Reviews ACS …
X Cui, X Xu, L Wojtas, MM Kim… - Journal of the American …, 2012 - ACS Publications
Co (III)–carbene radicals generated from activation of α-diazocarbonyls by Co (II)–porphyrin complexes have been shown to undergo a new type of tandem radical addition reaction with …
RL Yan, H Yan, C Ma, ZY Ren, XA Gao… - The Journal of …, 2012 - ACS Publications
A copper-catalyzed method for the synthesis of imidazo [1, 2-a] pyridines with aminopyridines and nitroolefins using air as oxidation agent in a one-pot procedure has …
RL Yan, J Luo, CX Wang, CW Ma… - The Journal of …, 2010 - ACS Publications
Cu (I)-Catalyzed Synthesis of Polysubstituted Pyrroles from Dialkyl Ethylenedicarboxylates and β-Enamino Ketones or Esters in t Page 1 DOI: 10.1021/jo101022k Published on Web 06/30/2010 …
R Yan, X Liu, C Pan, X Zhou, X Li, X Kang… - Organic letters, 2013 - ACS Publications
An efficient method for the direct synthesis of substituted quinolines from anilines and aldehydes through C–H functionalization, C–C/C–N bond formation, and C–C bond …
A Deepthi, BP Babu… - Organic Preparations and …, 2019 - Taylor & Francis
Furans constitute an important class of aromatic heterocycles displaying a wide range of pharmacological activities. 1–6 In addition, furans are the chief motifs of many natural …
S Manna, AP Antonchick - Organic letters, 2015 - ACS Publications
A synthesis of multisubstituted furans from readily available acetophenones and electron- deficient alkynes via direct C (sp3)–H bond functionalization under radical reaction …
M Feng, H Jiang, L Huang - Organic Chemistry Frontiers, 2022 - pubs.rsc.org
An efficient synthesis of polysubstituted furans by Ag (I)-mediated annulation between 5-H-1, 2, 3-thiadiazoles and 1, 3-dicarbonyl compounds is reported. The methodology was …
L Xiang, Y Yang, X Zhou, X Liu, X Li… - The Journal of …, 2014 - ACS Publications
A direct method for the synthesis of substituted indolizines by means of I2-mediated oxidative tandem cyclization via C–N/C–C bond formation was developed. Various …