Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Yoshiaki Tanabe"'
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Construction of stereogenic carbon centers of propargylic alcohols with free radicals could mark a simple route to molecular complexity from easily obtained starting materials. Here the authors present a strategy to control enantioselective propargyl
Externí odkaz:
https://doaj.org/article/1079e0cca84445d4a28170c1a4bebc7e
Publikováno v:
Asian Journal of Endoscopic Surgery.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a4417ba1a956b80423b046385cd4db4
https://doi.org/10.1111/ases.13200
https://doi.org/10.1111/ases.13200
Publikováno v:
Methods in Molecular Biology ISBN: 9781071630631
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db6db3cf8aa1627f3f2aadd2c508bc3e
https://doi.org/10.1007/978-1-0716-3064-8_7
https://doi.org/10.1007/978-1-0716-3064-8_7
Publikováno v:
The Journal of Organic Chemistry. 86:12577-12590
Cooperative photoredox- and nickel-catalyzed alkylative cyclization reactions of iodoalkynes with 4-alkyl-1,4-dihydropyridines as alkylation reagents under visible light irradiation have been achieved to afford the corresponding alkylated cyclopentyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e981802525066612f1d8ffc7ac5c0b4
https://doi.org/10.1021/acs.joc.1c01018
https://doi.org/10.1021/acs.joc.1c01018
Publikováno v:
Chemistry – A European Journal. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26debfd76368f645ac5784723d6feb6e
https://doi.org/10.1002/chem.202201546
https://doi.org/10.1002/chem.202201546
Publikováno v:
Angewandte Chemie. 133:11331-11336
The development of transition metal-catalyzed enantioselective propargylic substitution reactions has gained much progress in recent years, however, no successful example with phosphorus-centered nucleophiles has yet been reported until now. Herein,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d918497c4e8230fb7091fde07beeff7
https://doi.org/10.1002/ange.202102779
https://doi.org/10.1002/ange.202102779
Autor:
Yoshiaki Nishibayashi, Yoshiaki Tanabe
Publikováno v:
Chemical Society Reviews. 50:5201-5242
N2 is fixed as NH3 industrially by the Haber-Bosch process under harsh conditions, whereas biological nitrogen fixation is achieved under ambient conditions, which has prompted development of alternative methods to fix N2 catalyzed by transition meta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::474da7d81bae08f57e5676f15059a9f5
https://doi.org/10.1039/d0cs01341b
https://doi.org/10.1039/d0cs01341b
Autor:
Yoshiaki Tanabe, Yoshiaki Nishibayashi
Publikováno v:
Coordination Chemistry Reviews. 472:214783
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf2bd842dba298279773522e8865119b
https://doi.org/10.1016/j.ccr.2022.214783
https://doi.org/10.1016/j.ccr.2022.214783
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 27(63)
Ruthenium- and copper-catalyzed propargylic substitution reactions of propargylic alcohol derivatives with N-monosubstituted hydrazones as ambident nucleophiles are achieved in which N-monosubstituted hydrazones exhibit impressive different reactivit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f92417e06b16069d4c524c6f7a6614d3
https://pubmed.ncbi.nlm.nih.gov/34606139
https://pubmed.ncbi.nlm.nih.gov/34606139
Autor:
Yoshiaki Tanabe, Yoshiaki Nishibayashi
Publikováno v:
Coordination Chemistry Reviews. 389:73-93
Development of catalytic silylation of dinitrogen into silylamines using transition metal complexes under ambient reaction conditions precedes the development of catalytic transformation of dinitrogen into ammonia under ambient reaction conditions. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49698ca5139d03f12779b03962c83813
https://doi.org/10.1016/j.ccr.2019.03.004
https://doi.org/10.1016/j.ccr.2019.03.004