scholarly article | Q13442814 |
P356 | DOI | 10.1002/EJOC.201400033 |
P50 | author | Xavi Ribas | Q43419656 |
Imma Güell | Q63982972 | ||
P2860 | cites work | Rational Development of Practical Catalysts for Aromatic Carbon−Nitrogen Bond Formation | Q29544934 |
Computational explorations of mechanisms and ligand-directed selectivities of copper-catalyzed Ullmann-type reactions | Q34013661 | ||
Cu-catalyzed arylation of phenols: synthesis of sterically hindered and heteroaryl diaryl ethers | Q35124625 | ||
Diamine Ligands in Copper-Catalyzed Reactions | Q35786838 | ||
Copper-mediated coupling reactions and their applications in natural products and designed biomolecules synthesis | Q37242587 | ||
Copper/amino acid catalyzed cross-couplings of aryl and vinyl halides with nucleophiles | Q46432534 | ||
Highly functional group tolerance in copper-catalyzed N-arylation of nitrogen-containing heterocycles under mild conditions. | Q50603910 | ||
Carbon−Heteroatom Bond-Forming Reductive Eliminations of Amines, Ethers, and Sulfides | Q55951775 | ||
Catalytic CC, CN, and CO Ullmann-Type Coupling Reactions | Q56433059 | ||
Ueber Synthesen in der Biphenylreihe | Q56434485 | ||
Copper in cross-coupling reactions | Q56827849 | ||
Dimethyl Sulfoxide/Potassium Hydroxide: A Superbase for the Transition Metal-Free Preparation of Cross-Coupling Products | Q57404834 | ||
Ligand-Free Copper-CatalyzedN-Arylation of Nitrogen Nucleophiles | Q57404894 | ||
Caesium fluoride-promoted Stille coupling reaction: an efficient synthesis of 9Z-retinoic acid and its analogues using a practical building block | Q58007680 | ||
Investigating Spectrum of Biological Activity of 4- and 5-Chloro-2-hydroxy-N-[2-(arylamino)-1-alkyl-2-oxoethyl]benzamides | Q58260478 | ||
The role of organometallic copper(iii) complexes in homogeneous catalysis | Q59287892 | ||
Efficient iron/copper co-catalyzed arylation of nitrogen nucleophiles | Q79449000 | ||
A beta-keto ester as a novel, efficient, and versatile ligand for copper(I)-catalyzed C-N, C-O, and C-S coupling reactions | Q80155587 | ||
An Ullmann coupling of aryl iodides and amines using an air-stable diazaphospholane ligand | Q81438315 | ||
Transition-metal-free O-, S-, and N-arylation of alcohols, thiols, amides, amines, and related heterocycles | Q82979373 | ||
CuI/DMPAO-catalyzed N-arylation of acyclic secondary amines | Q84287237 | ||
Recyclable heterogeneous copper oxide on alumina catalyzed coupling of phenols and alcohols with aryl halides under ligand-free conditions | Q84416990 | ||
Photoinduced Ullmann C-N coupling: demonstrating the viability of a radical pathway | Q85336312 | ||
P433 | issue | 15 | |
P304 | page(s) | 3188-3195 | |
P577 | publication date | 2014-04-14 | |
P1433 | published in | European Journal of Organic Chemistry | Q899286 |
P1476 | title | Ligand-Free Ullmann-Type C-Heteroatom Couplings Under Practical Conditions | |
P478 | volume | 2014 |
Q41839368 | Synthesis, characterisation and reactivity of copper(I) amide complexes and studies on their role in the modified Ullmann amination reaction. | cites work | P2860 |
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