نتایج جستجو برای: organocopper compounds

تعداد نتایج: 226683  

Journal: :Journal of Synthetic Organic Chemistry, Japan 1991

Journal: :Journal of Synthetic Organic Chemistry, Japan 1996

2002
Ben L. Feringa Robert Naasz Rosalinde Imbos Leggy A. Arnold

Conjugate addition (1,4-addition) of carbon nucleophiles to a; b-unsaturated compounds is one of the most important carbon–carbon bond-forming strategies in synthetic organic chemistry [1]. The versatility of the conjugate addition is mainly due to the large variety of nucleophiles (organometallic reagents, Michael donors, other carbanions) and acceptors (a; b-unsaturated aldehydes, ketones, ni...

2011
Michael Stollenz Henrike Gehring Vera Konstanzer Stefan Fischer Sebastian Dechert Christian Grosse Franc Meyer

Organocopper chemistry has attracted considerable interest over the last few decades, which is attributed to its high and versatile potential in synthetic chemistry. This is, for instance, reflected by the unique role of copper in the activation of dioxygen, as demonstrated by important transformations such as the catalytic oxidation of ethylene to ethylene glycol, the Wacker process, and the o...

Journal: :Chemical communications 2003
James D White Chang-Sun Lee Qing Xu

The neurotoxic lipopeptide (+)-kalkitoxin was synthesized by a route which employed asymmetric organocopper conjugate addition followed by in situ enolate alkylation to install the anti,anti-1,2,4-trimethyl relationship of the toxin; the synthesis of kalkitoxin required sixteen steps and proceeded in 3% overall yield.

Journal: :Chemical communications 2015
Bijay Bhattarai Jia-Hui Tay Pavel Nagorny

A thiophosphoramide-based co-catalyst was found to significantly accelerate copper(II) trifluoromethanesulfonate-catalyzed arylation of potassium carboxylates with diaryliodonium salts. This effect could be attributed to counterion activation of diaryliodonium salts or organocopper intermediates by thiophosphoramides. Inclusion of thiophosphoramides permits achieving significantly milder reacti...

2016
Admilton G. de Oliveira Flavia R. Spago Ane S. Simionato Miguel O. P. Navarro Caroline S. da Silva André R. Barazetti Martha V. T. Cely Cesar A. Tischer Juca A. B. San Martin Célia G. T. de Jesus Andrade Cláudio R. Novello João C. P. Mello Galdino Andrade

Citrus canker is a very destructive disease of citrus species. The challenge is to find new compounds that show strong antibiotic activity and low toxicity to plants and the environment. The objectives of the present study were (1) to extract, purify and evaluate the secondary metabolites with antibiotic activity produced by Pseudomonas aeruginosa LV strain in vitro against Xanthomonas citri su...

Journal: :Journal of the American Chemical Society 2004
Douglas B Grotjahn DeWayne T Halfen Lucy M Ziurys Andrew L Cooksy

The most-studied organocopper, methylcopper (CH(3)Cu), has been synthesized for the first time as a monomer, free of other ligands or coordinated solvent, and detected using millimeter-wave rotational spectroscopy. The molecule was created in the gas phase by the reaction of copper vapor and several different precursors, including CH(4) and tetramethylsilane. An obvious symmetric top pattern wa...

Journal: :Organic letters 2016
Guillaume Guignard Núria Llor Elies Molins Joan Bosch Mercedes Amat

A convergent synthesis of fluvirucinin B1 from acid ent-6a and nitrile ent-9, involving an organocopper coupling, a stereoselective allylation, a ring-closing metathesis reaction, and a stereoselective hydrogenation as the key steps, is reported. The starting building blocks have been prepared in a straightforward manner from a common phenylglycinol-derived lactam 1. An unprecedented regioselec...

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