WebA tertiary amine-catalyzed formal (3+n) annulation of 2-(acetoxymethyl)buta-2,3-dienoate with 1,n-binucleophiles has been developed, which provides a facile entry to heterocyclic compounds. The mechanism, involving tandem SN2′–SN2′ substitution and Michael addition, has also been established. WebMar 22, 2013 · Cobalt-Catalyzed Oxidative Isocyanide Insertion to Amine-Based Bisnucleophiles: Diverse Synthesis of Substituted 2-Aminobenzimidazoles, 2 …
(PDF) On the reactivity of 6-acetyl-7-(2 ... - ResearchGate
WebAug 5, 2024 · The introduction of a methyl group and its 13 C and 2 H labeled analogs on Csp 2-centers remains a challenging issue in synthetic chemistry.While the photoredox/Ni dual catalysis has proven to constitute a valuable methodology for the forging of Csp 2 −Csp 3 bonds, the high difficulty to generate the methyl radical and to control its reactivity has … WebLiu, Jiaqi, "Cobalt-Catalyzed Aerobic Oxidative Cyclization Reactions of Bisnucleophiles: New Methodologies and the Role of Bisnucleophiles in O2 Activation" (2024). Graduate … irvine harvey counselling
On the Reactivity of N-Substituted Imidates Towards 1,4 …
WebA titanacarborane monoamide catalyzed, one-step synthesis of mono/bicyclic guanidines from commercially available di/triamines and carbodiimides is reported. The reaction mechanism is also proposed. WebOct 26, 2024 · A simple and efficient strategy has been established for the synthesis of δ-lactam fused oxindoles via the Michael/N-hemiketalization cascade reaction of 3-carboxamide oxindoles and α,β-unsaturated trifluoromethyl ketones.A wide range of structurally novel CF 3-containing spiro-δ-lactam oxindoles featuring acyl at the ortho … WebCobalt-Catalyzed Oxidative Isocyanide Insertion to Amine-Based Bisnucleophiles: Diverse Synthesis of Substituted 2-Aminobenzimidazoles, 2-Aminobenzothiazoles, and 2-Aminobenzoxazoles. Tong-Hao Zhu, Tong-Hao Zhu. portbase foutcode 92