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Les trépieds à cuve clouée
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Year: 1977 Volume: 3 Publisher: Paris : De Boccard,

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Tripods


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I tripodi a verghette in Etruria e in Italia centrale : origini, tipologia e caratteristiche
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ISBN: 9783884673195 9783795435165 Year: 2019 Publisher: Mainz : Verlag des Römisch-Germanischen Zentralmuseums,

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Dreifusskessel von Olympia : alte und neue Funde
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Year: 1957 Publisher: Berlin : De Gruyter,

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Bronze tripods and related stands in the Eastern Mediterranean from the twelfth through the seventh centuries B.C.
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Year: 1977 Publisher: Ann Arbor, Mich. : University Microfilms International,

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Dreifusskessel von Olympia : alte und neue Funde
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Year: 1957 Volume: 3 Publisher: Berlin : W. de Gruyter,

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Darstellungen von Dreifußkesseln in der griechischen Kunst bis zum Beginn der Klassischen Zeit.
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ISBN: 3631318227 Year: 1997 Publisher: Frankfurt am Main Lang

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A Note on Rubens's Letter on Tripods

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Les trépieds du Ptoion
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Year: 1943 Volume: fasc. 153 Publisher: Paris : E. de Boccard,

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Die geometrischen Dreifüsse von Olympia
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ISBN: 311006703X 9783110067033 Year: 1978 Volume: 10 Publisher: Berlin ; New York, NY : Walter de Gruyter,


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Advances in Cross-Coupling Reactions
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Year: 2020 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

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In this Special Issue, recent advances in cross-coupling reactions are presented in the form of original research articles, reviews, and short communications. These contributions cover different topics in this area, including novel coupling reactions, reaction conditions, synthetic alternatives, metal ligands, and applications for new pharmaceutical compounds and organic materials. In particular, the reviews deal with methodologies such as the synthesis of diarylketones through palladium catalysis and the most relevant examples of Suzuki–Miyaura and Buchwald–Hartwig coupling reactions in the synthesis of bioactive compounds. The synthetic utility of cross-coupling reactions for the synthesis of medium-size rings and the utility of Stille and Suzuki coupling reactions for the synthesis of new molecular machines based on sterically hindered anthracenyl trypticenyl units are also summarized. The original research articles present the synthesis of 2-alkynylpyrrols by inverse Sonogashira coupling and the synthesis of indoles under oxidative dearomative cross-dehydrogenative conditions. The efficient combination of iridium-catalyzed C–H borylation of aryl halides with the Sonogashira coupling and a sequential iridium-catalyzed borylation of NH-free pyrroles followed by a Suzuki–Miyaura reaction are included. The synthesis of aryl propionic acids, a common structural motif in medicinal chemistry, and the synthesis of new organic dyes are also covered.

Keywords

Research & information: general --- cross coupling --- dearomatization --- C-H functionalization --- indolin-3-ones --- dimerization and trimerization of indoles --- C-H borylation --- Sonogashira cross-coupling --- borylated aryl alkynes --- one-pot reaction --- restricted rotations --- M(CO)3 tripods --- molecular brakes and gears --- X-ray --- V-T NMR --- borylation --- Suzuki coupling --- NH-Free --- 5-aryl pyrrole-2-carboxylates --- iridium-catalyzed --- heteroaryl substituted pyrroles --- 2,3'-bipyrrole --- electrophilic haloacetylenes --- pyrroles --- ethynylpyrroles --- furans --- thiophenes --- pyrazoles --- Al2O3 --- transition-metal catalysis --- intramolecular cyclization --- medium-sized heterocycles --- C-H activation --- acylation --- palladium --- arenes --- heteroarenes --- indigo dyes --- DSSC --- synthesis --- spectroscopy --- Heck reaction --- styrene --- methoxycarbonylation --- profene --- cross-coupling reactions --- C-C bond forming reactions --- C-Heteroatom bond forming reactions --- clinical candidate --- DNA-encoded libraries --- cyclopeptides --- allosteric modulators --- PROTAC --- catalysis in water --- C-C cross-coupling --- Suzuki-Miyaura reaction --- sulfonated salan --- cross coupling --- dearomatization --- C-H functionalization --- indolin-3-ones --- dimerization and trimerization of indoles --- C-H borylation --- Sonogashira cross-coupling --- borylated aryl alkynes --- one-pot reaction --- restricted rotations --- M(CO)3 tripods --- molecular brakes and gears --- X-ray --- V-T NMR --- borylation --- Suzuki coupling --- NH-Free --- 5-aryl pyrrole-2-carboxylates --- iridium-catalyzed --- heteroaryl substituted pyrroles --- 2,3'-bipyrrole --- electrophilic haloacetylenes --- pyrroles --- ethynylpyrroles --- furans --- thiophenes --- pyrazoles --- Al2O3 --- transition-metal catalysis --- intramolecular cyclization --- medium-sized heterocycles --- C-H activation --- acylation --- palladium --- arenes --- heteroarenes --- indigo dyes --- DSSC --- synthesis --- spectroscopy --- Heck reaction --- styrene --- methoxycarbonylation --- profene --- cross-coupling reactions --- C-C bond forming reactions --- C-Heteroatom bond forming reactions --- clinical candidate --- DNA-encoded libraries --- cyclopeptides --- allosteric modulators --- PROTAC --- catalysis in water --- C-C cross-coupling --- Suzuki-Miyaura reaction --- sulfonated salan

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