Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Kyosuke Kaneda"'
Publikováno v:
Journal of Natural Medicines. 77:276-283
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::404c00fc079bda2e045a49fef54b844f
https://doi.org/10.1007/s11418-022-01667-6
https://doi.org/10.1007/s11418-022-01667-6
Publikováno v:
Chemistry Letters; Jan2024, Vol. 53 Issue 1, p1-4, 4p
Autor:
Kyosuke Kaneda
Publikováno v:
YAKUGAKU ZASSHI. 140:1087-1094
This review, based on my research work, introduces and summarizes the synthesis and characterization of novel cyclic compounds containing aminobenzenesulfonamide. The review discusses the (1) development of sequential Nicholas and Pauson-Khand reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2ba894a2b0ca9b1b8f8315750697200
https://doi.org/10.1248/yakushi.20-00139
https://doi.org/10.1248/yakushi.20-00139
Publikováno v:
Asian Journal of Organic Chemistry. 7:793-801
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433bb7b9d4fe8f573039600e910cd837
https://doi.org/10.1002/ajoc.201700687
https://doi.org/10.1002/ajoc.201700687
Publikováno v:
Synthetic Communications. 47:1622-1629
The intramolecular Pauson-Khand cyclization in the presence of both aniline and nitrobenzene was used to improve the construction of N-nitrobenzenesulfonyl (Ns)-protected 3-azabicyclo[4.3.0]nonane skeletons. We found that aniline enhanced the cycliza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ae75daee77fe355a7695840c3ae1ad9
https://doi.org/10.1080/00397911.2017.1337151
https://doi.org/10.1080/00397911.2017.1337151
Publikováno v:
Organic Letters. 19:1096-1099
The synthesis of 2-aminobenzenesulfonamide-containing cyclononyne (ABSACN), starting from 2-nitrobenzenesulfonamide and but-2-yne-1,4-diol via Mitsunobu and Nicholas reactions, is described for the development of an adjustable alkyne reagent in click
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2561d2f1be540a160fac4c56ad4ab068
https://doi.org/10.1021/acs.orglett.7b00123
https://doi.org/10.1021/acs.orglett.7b00123
Universal HPLC Detector for Hydrophilic Organic Compounds by Means of Total Organic Carbon Detection
Publikováno v:
Analytical chemistry. 90(11)
Most quantifications are achieved by comparison of the signals obtained with the sample to those from a standard. Thus, the purity and stability of the standard are key in chemical analysis. Furthermore, if an analyte standard cannot be obtained, qua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc907d06c7df611ab55b36fd97e3ac6f
https://pubmed.ncbi.nlm.nih.gov/29733193
https://pubmed.ncbi.nlm.nih.gov/29733193
Publikováno v:
Tetrahedron Letters. 56:4674-4677
We have developed an exceptional one-pot domino cyclization process, in which a nitroarene reduction step initiates an endocyclic Nicholas reaction followed by an intramolecular Pauson–Khand cyclization. Remarkably, all reactions in this process ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d93402b02f0aaa0933d199ea167eac39
https://doi.org/10.1016/j.tetlet.2015.06.038
https://doi.org/10.1016/j.tetlet.2015.06.038
Publikováno v:
ACS Combinatorial Science. 15:379-386
A strategy involving a Mannich-type multicomponent assembly process followed by a 1,3-dipolar cycloaddition has been developed for the rapid and efficient construction of parent heterocyclic scaffolds bearing indole and isoxazolidine rings. These key
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79f4ad5ae3f49d5a027984d6900cf93f
https://doi.org/10.1021/co400055b
https://doi.org/10.1021/co400055b
Publikováno v:
ACS Combinatorial Science. 14:75-79
A Mannich-type multicomponent assembly process/1,3-dipolar cycloaddition strategy has been developed for the rapid and efficient construction of a parent tetrahydroisoquinoline fused isoxazolidine scaffold, which was subsequently functionalized using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::539f1a7e81cee43968c97eeddf21b8e9
https://doi.org/10.1021/co2001636
https://doi.org/10.1021/co2001636