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作 者:Wei Fu Valentina Pelliccioli Raquel Casares-López Juan M.Cuerva Martin Simon Christopher Golz Manuel Alcarazo
机构地区:[1]Institut für Organische und Biomolekulare Chemie,Georg-August-Universität Göttingen,37077 Göttingen [2]Departamento de Química Orgánica,Universidad de Granada,Unidad de Excelencia Química Aplicada a Biomedicina y Medioambiente,E-18071 Granada
出 处:《CCS Chemistry》2024年第10期2439-2451,共13页中国化学会会刊(英文)
基 金:the Deutsche Forschungsgemeinschaft(INST 186/1352-1 and INST 186/1237-1)is gratefully acknowledged.W.F;thanks the China Scholarship Council for PhD fellowship support.R.C.-L.gratefully acknowledges grant PID2021-127964NB-C22 funded by the MCIN/AEI/10.13039/501100011033.
摘 要:An expedient synthesis of a series of configurationally stable oxa[5]helicenes,oxa[6]helicenes,and dioxa[6]helicenes has been developed using an intramolecular,highly enantioselective,Au-catalyzed,alkyne hydroarylation reaction.The absolute configuration of the newly prepared structures has been established by crystallography,their inversion barriers have been determined theoretically and experimentally,and their chiroptical properties have been investigated.Comparison of these data with those reported for thia-or carbohelicenes sharing an otherwise identical helical framework enables the establishment of comprehensive correlations between the nature of the embedded(hetero)atom(s)and the magnitude of these properties.Preliminary studies on the postsynthetic functionalization of the oxahelicenes obtained are also described.Specifically,siteselective bromination at the 15-position in oxa[5]helicene 5d allows its subsequent manipulation into pyridine-containing aza-oxa[7]helicene 13d;while the two termini of oxa[6]helicene 7d have been intramolecularly cyclised into the pleiadeno[1,12,11-bcde]benzofuran derivative 15d by acidic treatment.Both transformations take place without erosion of the enantiopurity.
关 键 词:Au-catalysis enantioselective synthesis oxa[n]helicenes racemization dynamics postsynthetic functionalization
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