Zobrazeno 1 - 10
of 178
pro vyhledávání: '"Jun-ichi Matsuo"'
Publikováno v:
ARKIVOC, Vol 2004, Iss 3, Pp 42-65 (2003)
Externí odkaz:
https://doaj.org/article/ead0695bccec47be8bc63bb867f8882b
Publikováno v:
ARKIVOC, Vol 2001, Iss 10, Pp 58-65 (2001)
Externí odkaz:
https://doaj.org/article/65d0f14ecfa345dea426359c4a1b5d36
Publikováno v:
Synlett. 33:1519-1522
A synthesis of 3-alkyl-2-arylindoles was performed by sequential oxidation and reduction of 2-(2-nitrophenyl)ethanols that were prepared by base-catalyzed three-component reactions of vinylarenes, aldehydes, and various pronucleophiles, including nit
Publikováno v:
Organic Chemistry Frontiers. 9:3786-3793
Regio-, stereo- and enantioselective cascade intramolecular aldol cyclization/acetalizations of symmetrical 1,2,7,8-tetraones were developed. The total synthesis of (±)-nesteretal A was accomplished in seven steps by this synthetic strategy.
Publikováno v:
European Journal of Organic Chemistry. 2021:850-853
Publikováno v:
Green Chemistry. 23:1160-1164
Three-component reactions of nitroalkanes, acrylamides, and aldehydes by using a catalytic amount of KOH in DMSO gave β′-hydroxy-γ-nitro amides. Mechanistic studies suggested that the reactions proceeded by domino Michael/aldol reactions. The hig
Publikováno v:
Chemical and Pharmaceutical Bulletin. 68:1201-1209
Regioselectivity for intramolecular Diels-Alder (IMDA) reactions of 6-acetoxy-6-alkenylcyclohexa-2,4-dien-1-ones that were formed by oxidation of 2-alkenylphenols with lead tetraacetate in acetic acid were studied. Bridged regioselectivity was observ
Publikováno v:
European Journal of Organic Chemistry. 2020:6649-6652
Autor:
Takahiro Ishimoto, Yukio Kato, Noritaka Nakamichi, Misa Nishiyama, Jun-ichi Matsuo, Tomoyuki Yoshimura, Tomoe Komori, Yusuke Masuo
Publikováno v:
Neurochemical Research. 45:2664-2678
Understanding of the underlying mechanism of epilepsy is desired since some patients fail to control their seizures. The carnitine/organic cation transporter OCTN1/SLC22A4 is expressed in brain neurons and transports food-derived antioxidant ergothio
Publikováno v:
Synthesis. 52:3667-3674
The enantioselective synthesis of a bicyclo[4.3.0]nonene derivative bearing a quaternary carbon stereocenter is achieved by employing a desymmetrization strategy involving an intramolecular addition. The intramolecular nucleophilic addition of a high