Zobrazeno 1 - 10
of 327
pro vyhledávání: '"Kozo Shishido"'
Autor:
Tomoyuki Yoshimura, Hidetoshi Kisyuku, Tomoyo Kamei, Kenya Takabatake, Mitsuru Shindo, Kozo Shishido
Publikováno v:
ARKIVOC, Vol 2003, Iss 8, Pp 247-255 (2003)
Externí odkaz:
https://doaj.org/article/64389fea9f5d4ec8ba760ac639b6907a
Publikováno v:
The Journal of Organic Chemistry. 79:7512-7519
The first enantioselective total synthesis of penostatin E has been accomplished. Two highly efficient and diastereoselective reactions, a Hosomi-Sakurai allylation and an intramolecular Pauson-Khand reaction, were utilized for the construction of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::073b62f4e3c15140e38ec56fc5dcdb6b
https://doi.org/10.1021/jo501225y
https://doi.org/10.1021/jo501225y
Publikováno v:
Tetrahedron. 69:5273-5280
Oxidative radical cyclization of cyclic β-keto esters with alkenes is described. Substituted hydroxyhexahydrocyclopenta[b]furancarboxylates having substituents at the 2-position were produced in a diastereoselective manner when the reactions were ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ed2470939198eebff1236761a5b4638
https://doi.org/10.1016/j.tet.2013.05.005
https://doi.org/10.1016/j.tet.2013.05.005
Publikováno v:
The Journal of Organic Chemistry. 78:1687-1692
The reaction of propargylic carbonates with 4-hydroxy-2-pyrones in the presence of a palladium catalyst is described. By the choice of the reaction temperature, two types of the substituted furo[3,2-c]pyran-4-one derivatives were regioselectively syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be2128ad2777a81c0be8d717183b6cf7
https://doi.org/10.1021/jo3027092
https://doi.org/10.1021/jo3027092
Autor:
Hiromasa Yokoe, Makoto Kanematsu, Takaaki Araki, Kozo Shishido, Tsukasa Ozawa, Masahiro Yoshida
Publikováno v:
Organic Letters. 15:200-203
A novel and highly diastereoselective intramolecular carbamoylketene/alkene [2 + 2] cycloaddition has been developed, and the methodology was successfully applied to the enantioselective syntheses of (-)-esermethole and Takayama's intermediate for (+
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85483b937316bde740d275df9d136909
https://doi.org/10.1021/ol303204v
https://doi.org/10.1021/ol303204v
Publikováno v:
Synlett. 24:61-64
The second generation synthesis of (+)-aspermytin A and the first total synthesis of (–)-oblongolide C have been accomplished employing an intramolecular nitrile oxide–alkene [3+2] cycloaddition as the key step.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c662ac83387e3e0e0bce29bcf79e8cdd
https://doi.org/10.1055/s-0032-1317693
https://doi.org/10.1055/s-0032-1317693
Publikováno v:
Tetrahedron. 68:9962-9972
A palladium-catalyzed cyclization of 2-amidophenylmalonates with allylic bisacetates is described. Tetrahydroquinolines having a vinyl group at the 3- or 2-position were produced, in which the regioselectivity of the resulting products was altered de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac66442c80e880e407e77a1eb484e9f6
https://doi.org/10.1016/j.tet.2012.09.075
https://doi.org/10.1016/j.tet.2012.09.075
Publikováno v:
Chemistry - A European Journal. 18:15578-15581
This'll fix it: efficient fixation of atmospheric CO(2) has been achieved by the reaction of propargylic amines with a silver/DBU dual-catalyst system. Various oxazolidinones were synthesized in moderate to good yields by using substituted propargyli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32413f44dd2f3ace7d66ad10f4d326c6
https://doi.org/10.1002/chem.201203366
https://doi.org/10.1002/chem.201203366
Autor:
Yuki Manabe, Hiromasa Yokoe, Masahiro Yoshida, Makoto Kanematsu, Akari Miyawaki, Daisuke Kikuchi, Kozo Shishido, Masu Niki
Publikováno v:
The Journal of Organic Chemistry. 77:8231-8243
A full account of the development of a novel type of the intramolecular Hosomi-Sakurai reactions of the substrates with a p-benzoquinone and an allylsilane moieties connected by an ether linkage is described. This transformation proceeds via an addit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d2307e393081f71173243ddb407117
https://doi.org/10.1021/jo3016055
https://doi.org/10.1021/jo3016055
Publikováno v:
Tetrahedron Letters. 53:1236-1239
The first enantiocontrolled total synthesis of heliespirone B has been accomplished employing a biomimetic intramolecular oxy-Michael reaction followed by the regio- and diastereoselective reduction of the carbonyl function as key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93e00589ed6c2b4bb5943e2558ee92ca
https://doi.org/10.1016/j.tetlet.2011.12.115
https://doi.org/10.1016/j.tetlet.2011.12.115