Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Yasunori Minami"'
Publikováno v:
Organic Letters. 21:9019-9023
A synthetic method for diverse γ-aryl-β-ketoesters through γ-aryl-β-ketoester-type arynes triggered by C-C bond cleavage has been developed. The Mukaiyama aldol reaction of 6-(triflyloxy)benzocyclobutenones with ketene silyl acetals and subsequen
Autor:
Tamejiro Hiyama, Yasunori Minami
Publikováno v:
Chemistry – A European Journal. 25:391-399
Organo(trialkyl)silanes have several advantages, including high stability, low toxicity, good solubility, easy handling, and ready availability compared with heteroatom-substituted silanes. However, methods for the cross-coupling of organo(trialkyl)s
Publikováno v:
Chemistry Letters. 47:1288-1291
Synthesis of 1-substituted 1-siloxy-3-aryloxybuta-1,3-dienes is achieved starting with readily available methyl ketones by a reaction sequence involving a palladium-catalyzed addition of the ketone...
Autor:
Yasunori Minami, Albert Poater, Giovanni Talarico, Martí Gimferrer, Tamejiro Hiyama, Massimo Christian D'Alterio
The mechanism for the synthesis of 2,3-bismethylenechromanes obtained by the reaction between silylethynyloxyarenes and allylic pivalates and catalyzed by a palladium complex has been investigated using computational methods rooted in density functio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eedeee07a348e03fc8d4f443e2cd820
http://hdl.handle.net/11588/832443
http://hdl.handle.net/11588/832443
Publikováno v:
Asian Journal of Organic Chemistry. 7:1343-1346
Publikováno v:
Organometallics. 37:1456-1461
Understanding the formation of benzosiloles by the intramolecular palladium-catalyzed annulation of alkynyl(aryl)silanes is crucial for achieving synthetic diversity toward the enhancement of the chemistry of siloles. By a combination of density func
Publikováno v:
Chemistry Letters. 48:361-363
Aryl(triethyl)silanes were found to cross-couple with aryl chlorides by palladium/copper dual catalysis and XPhos as a crucial ligand. The catalyst system is applicable to a facile oligothiophene s...
Publikováno v:
Chemistry Letters. 46:899-902
Stable benzopyrylium tetrafluoroborates, prepared by palladium-catalyzed annulation of aryl triisopropylsilylethynyl ethers with internal alkynes followed by BF3·OEt2 treatment, exhibited solid-state luminescence upon UV irradiation.
Autor:
Tamejiro Hiyama, Takeshi Komiyama, Osamu Goto, Shu-ichi Uno, Hideyuki Ikehira, Yasunori Minami, Kenta Shimizu
Publikováno v:
Synlett. 28:2407-2410
Nickel-catalyzed N-arylation reaction of N-trimethylsilyl-carbazole using aryl bromides is found to proceed in the presence of sodium acetate, giving N-aryl-carbazoles in high yields. Under these conditions, N-trimethylsilyl-carbazole could react wit
Publikováno v:
Synlett. 28:1873-1884
The silicon-based cross-coupling reaction has attracted much attention over recent decades because there are many advantages in using organosilicon compounds. However, the use of reagents with a triorganosilyl group as a key function remains to be es