Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Saki Maejima"'
Publikováno v:
ACS Omega, Vol 4, Iss 3, Pp 4856-4870 (2019)
Externí odkaz:
https://doaj.org/article/e29ec744eb8c441fad5929c7b641561d
Publikováno v:
Bulletin of the Chemical Society of Japan; Apr2024, Vol. 97 Issue 4, p1-5, 5p
Publikováno v:
Organic Letters. 25:1856-1861
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::376dc2982b45c35304bb62c7f926285f
https://doi.org/10.1021/acs.orglett.3c00335
https://doi.org/10.1021/acs.orglett.3c00335
Publikováno v:
Angewandte Chemie. 134
Neaumycin B is a femtomolar inhibitor of U87 human glioblastoma. Using a newly developed anti-diastereoselective ruthenium-catalyzed butadiene-mediated crotylation of primary alcohol proelectrophiles via hydrogen auto-transfer, as well as a novel var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eaae110d87eaefb315a6d0275413ea7
https://doi.org/10.1002/ange.202214786
https://doi.org/10.1002/ange.202214786
A method for the catalytic regioselective synthesis of C3-substituted dihydrobenzofurans (DHBs) via [2+2] photocycloaddition of alkene and p-benzoquinone is developed. This method realizes the rapid synthesis of DHBs with readily available substrates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46d363eeebdf96a4b9050b9c8787a4b9
https://doi.org/10.26434/chemrxiv-2022-rx5pd
https://doi.org/10.26434/chemrxiv-2022-rx5pd
Publikováno v:
Asian Journal of Organic Chemistry. 9:571-574
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a3f0807a967e3f436f1544e022406e6
https://doi.org/10.1002/ajoc.202000041
https://doi.org/10.1002/ajoc.202000041
Publikováno v:
Asian Journal of Organic Chemistry. 9:210-213
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a0b92d5f62c175ee871165f163c880c
https://doi.org/10.1002/ajoc.202000022
https://doi.org/10.1002/ajoc.202000022
Publikováno v:
ACS Omega
ACS Omega, Vol 4, Iss 3, Pp 4856-4870 (2019)
ACS Omega, Vol 4, Iss 3, Pp 4856-4870 (2019)
This study aims to develop an intermolecular lactonization reaction of alkenes with carbonyls mediated by visible light and molecular iodine. The one-step reaction involved the carboesterification of alkenes to produce the corresponding lactones in m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::869469faec18d9dd0e5400bf699d156e
http://europepmc.org/articles/PMC6648839
http://europepmc.org/articles/PMC6648839
Publikováno v:
The Journal of organic chemistry. 85(16)
A novel three-component γ-iminolactonization reaction was developed, which relied on the C-C/C-O bond-forming bifunctionalization of olefins using molecular iodine and visible light. This strategy did not require any (heavy) metal reagents for doubl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::025f8bb1a8fd84766da676da25a3089e
https://pubmed.ncbi.nlm.nih.gov/32806099
https://pubmed.ncbi.nlm.nih.gov/32806099
Publikováno v:
Tetrahedron. 74:2985-2990
The iodine/DMAP-mediated intramolecular tandem C–C/C–O bond forming reaction of malonate bearing alkene moiety proceeded to give bicyclic lactones with good diastereoselectivity in good yield. The mechanistic investigation was also discussed on t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9707c7ed9c7c9e137bf80aa2d58ac92b
https://doi.org/10.1016/j.tet.2018.04.081
https://doi.org/10.1016/j.tet.2018.04.081