Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ken Okuno"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 1794-1799 (2024)
Enantioselective halolactonizations of sterically less hindered alkenoic acid substrates without substituents on the carbon–carbon double bond have remained a formidable challenge. To address this limitation, we report herein the asymmetric bromola
Externí odkaz:
https://doaj.org/article/0d7d1923cde544ed88840e116616e919
Publikováno v:
Tetrahedron Chem, Vol 6, Iss , Pp 100037- (2023)
The synthetic utility of onium salts is widely recognized in organic chemistry. Among the wide variety of onium salt compounds, quaternary ammonium and phosphonium salts are known as representative organocatalysts. Although the catalytic abilities of
Externí odkaz:
https://doaj.org/article/884d3194156b4a7ab0243cc354162638
Publikováno v:
Advanced Synthesis & Catalysis. 365:1496-1504
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c8ce66bf8742e1ccd6d0a2ca6383531
https://doi.org/10.1002/adsc.202300145
https://doi.org/10.1002/adsc.202300145
Publikováno v:
Organic & Biomolecular Chemistry. 21:3263-3275
Recent advances in chiral sulfide-catalyzed asymmetric halocyclizations are summarized.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d2b2268db3093a1f30fc08f4311a317
https://doi.org/10.1039/d3ob00292f
https://doi.org/10.1039/d3ob00292f
Publikováno v:
Chemical and Pharmaceutical Bulletin. 70:599-604
1,1′-Bi-2-naphthol (BINOL)-derived chiral bifunctional sulfide and selenide catalysts that possess a hydroxy group are known to be effective catalysts for enantioselective bromolactonizations. When applied to asymmetric iodolactonizations of 4-pent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::560a8e389c1ae020afeec09b34a25cc4
https://doi.org/10.1248/cpb.c22-00049
https://doi.org/10.1248/cpb.c22-00049
Publikováno v:
Chirality. 34:915-924
Although the wide variety of heterocyclic compounds is common knowledge, chiral 2-oxazolidinones are recognized as some of the most important heterocycles in medicinal chemistry. Many important pharmaceutical molecules have been constructed based on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::222cfca02f79ca895834712b96d676f2
https://doi.org/10.1002/chir.23452
https://doi.org/10.1002/chir.23452
Publikováno v:
Bulletin of the Chemical Society of Japan. 95:52-58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f38da8e559af898037844da2b5275132
https://doi.org/10.1246/bcsj.20210347
https://doi.org/10.1246/bcsj.20210347
Publikováno v:
Asian Journal of Organic Chemistry. 10:655-659
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f181740283c7aebc3fe67f9c176b29c
https://doi.org/10.1002/ajoc.202100001
https://doi.org/10.1002/ajoc.202100001
Publikováno v:
Chemical Communications. 57:10907-10910
Asymmetric halolactonizations are powerful methods for the syntheses of chiral lactones. Catalytic and highly enantioselective halolactonizations of α-allyl carboxylic acids, however, continue to present a formidable challenge. Herein, we report the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ac3a693baf792e01d6f4c7b6d6baf6a
https://doi.org/10.1039/d1cc03874e
https://doi.org/10.1039/d1cc03874e
Publikováno v:
Chemistry – An Asian Journal. 15:463-472
The synthetic utility of alkyl-onium salt compounds is widely recognized in the field of organic chemistry. Among the wide variety of onium salts, quaternary ammonium, phosphonium, and tertiary sulfonium salts have been the most useful compounds in o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c39abd39a99953324a66a555f212fa6
https://doi.org/10.1002/asia.201901652
https://doi.org/10.1002/asia.201901652