00968nam a22002291i 450099100272214970753620040604160747.0040624s1964 rm a||||||||||||||||rum b12967750-39ule_instARCHE-092543ExLDip.to Beni CulturaliitaA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l.Aricescu, Andrei487229Noi monumente epigrafice din Scythia Minor /A. Aricescu ... [et al.] ; cuvint inainte C. DaicoviciuConstanta :Muzeul regional de arheologie Dobrogea,1964188 p. :ill. ;21 cmDaicoviciu, Constantin.b1296775002-04-1412-07-04991002722149707536LE001 D Ad. 2312001000088096le001C. 1-E0.00-l- 00000.i1356982x12-07-04Noi monumente epigrafice din Scythia Minor279134UNISALENTOle00112-07-04ma -rumrm 0104506nam 2201045z- 450 991055731670332120210501(CKB)5400000000042688(oapen)https://directory.doabooks.org/handle/20.500.12854/69364(oapen)doab69364(EXLCZ)99540000000004268820202105d2020 |y 0engurmn|---annantxtrdacontentcrdamediacrrdacarrierAdvances in Cross-Coupling ReactionsBasel, SwitzerlandMDPI - Multidisciplinary Digital Publishing Institute20201 online resource (234 p.)3-03943-567-1 3-03943-568-X 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.Research and information: generalbicssc2,3'-bipyrrole5-aryl pyrrole-2-carboxylatesacylationAl2O3allosteric modulatorsarenesborylated aryl alkynesborylationC-C bond forming reactionsC-C cross-couplingC-H activationC-H borylationC-H functionalizationC-Heteroatom bond forming reactionscatalysis in waterclinical candidatecross couplingcross-coupling reactionscyclopeptidesdearomatizationdimerization and trimerization of indolesDNA-encoded librariesDSSCelectrophilic haloacetylenesethynylpyrrolesfuransHeck reactionheteroarenesheteroaryl substituted pyrrolesindigo dyesindolin-3-onesintramolecular cyclizationiridium-catalyzedM(CO)3 tripodsmedium-sized heterocyclesmethoxycarbonylationmolecular brakes and gearsn/aNH-Freeone-pot reactionpalladiumprofenePROTACpyrazolespyrrolesrestricted rotationsSonogashira cross-couplingspectroscopystyrenesulfonated salanSuzuki couplingSuzuki-Miyaura reactionsynthesisthiophenestransition-metal catalysisV-T NMRX-rayResearch and information: generalPérez Sestelo Joséedt1326443Sarandeses Luis AedtPérez Sestelo JoséothSarandeses Luis AothBOOK9910557316703321Advances in Cross-Coupling Reactions3037438UNINA