Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Kyosuke, Kaneda"'
Publikováno v:
Journal of Natural Medicines. 77:276-283
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
Publikováno v:
Asian Journal of Organic Chemistry. 7:793-801
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
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
Autor:
Teppei Sato, Kyosuke Kaneda, Ayaka Fujii, Syuji Ishikawa, Tatsuya Okazaki, Fuma Kamada, Ryoki Nogiwa, Nozomi Akimura, Syota Yamamoto
Publikováno v:
Synthesis. 48:3931-3940
Unique tetracyclic molecules containing heteroatom-embedded, medium-sized rings were synthesized by employing cascade Nicholas and Pauson–Khand cyclization reactions. We successfully established a divergent synthetic route for quick access to unpre
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
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
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