Zobrazeno 1 - 10
of 896
pro vyhledávání: '"TAMEJIRO HIYAMA"'
Publikováno v:
ARKIVOC, Vol 2007, Iss 10, Pp 29-48 (2006)
Externí odkaz:
https://doaj.org/article/0564702223b043bc943091bc6ed00f70
Autor:
Yasunori Minami, Tamejiro Hiyama
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 79:642-651
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87471cbfddf396fc81ca3b7c71f42c1d
https://doi.org/10.5059/yukigoseikyokaishi.79.642
https://doi.org/10.5059/yukigoseikyokaishi.79.642
Publikováno v:
Organosilicon Chemistry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3b1582d283655288e7f5033072009fd
https://doi.org/10.1002/9783527814787.ch9
https://doi.org/10.1002/9783527814787.ch9
Facile Construction of Furanoacenes by a Three-Step Sequence Going through Disilyl-exo-cyclic Dienes
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 26(43)
Facile synthesis of various benzonaphthofurans was achieved by intramolecular hydroarylation of 1,4-disilyl-2-aryloxy-1,3-enynes followed by cycloaddition with arynes or alkenes and finally desilylaromatization. The three-step transformation can be o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dfb90128dadce3e43f8d4152c3bc8bf
https://pubmed.ncbi.nlm.nih.gov/32181527
https://pubmed.ncbi.nlm.nih.gov/32181527
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb63af880c6055efba0e5fa1e7607983
https://doi.org/10.1002/chem.201803213
https://doi.org/10.1002/chem.201803213
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...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5481d69fc5e97a4c5a184691f6679fcf
https://doi.org/10.1246/cl.180582
https://doi.org/10.1246/cl.180582
Publikováno v:
Asian Journal of Organic Chemistry. 7:1343-1346
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bb3502a38b6763a01ab44e21f236ce0
https://doi.org/10.1002/ajoc.201800234
https://doi.org/10.1002/ajoc.201800234
Autor:
Yuichiro Tokoro, Takashi Mitsui, Shin-ichi Fukuzawa, Ryosuke Haraguchi, Kengo Sugita, Tamejiro Hiyama, Masato Harada, Yasunori Minami
Publikováno v:
Bulletin of the Chemical Society of Japan. 91:839-845
We have developed palladium-catalyzed C–H activation and cyclization of alkynyl ferrocenyl ethers with various alkynes, providing ferrocene-fused pyran derivatives. As a preliminary result, we also achieved the asymmetric version of this reaction w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d56b960921a3ecacc5640a799952b217
https://doi.org/10.1246/bcsj.20170415
https://doi.org/10.1246/bcsj.20170415
Publikováno v:
Chemistry Letters. 47:674-677
Palladium/carboxylic acid-catalyzed alkenylation of heteroarenes and electron-deficient arenes using alkynes underwent C(sp2)–H bond activation in arene substrates to give the corresponding alkenylarenes straightforwardly. The versatility of this t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d22baac00e148021f724e05238b27e0
https://doi.org/10.1246/cl.180143
https://doi.org/10.1246/cl.180143
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6dc2c523ca8dd12b42953c04587c190
https://doi.org/10.1021/acs.organomet.8b00102
https://doi.org/10.1021/acs.organomet.8b00102