Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Hiroto, Kaku"'
Publikováno v:
New Journal of Chemistry. 46:16256-16259
A base-induced isomerization of red uroleuconaphin A1 to yellow uroleuconaphin A2 having polycyclic acetal is described here.
Autor:
Chiharu Ozakai, Kei Kitamura, Mitsuyo Horikawa, To-sho Hoshiyama, Akari Imamura, Tatsuro Yoneyama, Akemi Umeyama, Masaaki Noji, Tetsuto Tsunoda, Hiroto Kaku
Publikováno v:
New Journal of Chemistry. 46:2600-2604
A strong acid-promoted single-step transformation of red uroleuconaphin A1 to green viridaphins A1 and A2 is described here.
Silica gel-mediated chemical degradation of dimeric pyranonaphthoquinones into their monomeric units
Publikováno v:
New Journal of Chemistry.
A chemical degradation of dimeric pyranonaphthoquinones mediated by silica gel into their monomeric units is described here.
Autor:
Kei Kitamura, Tetsuto Tsunoda, Hiroto Kaku, Taichi Nishimura, Hinano Kanagawa, Hayato Tokuda, Chiharu Ozakai
Publikováno v:
Synthesis. 53:1629-1635
A stereoselective synthesis of a pyranonaphthoquinone derivative found in aromatic polyketide-derived aphid pigments is reported herein. This approach features the anionic [4+2]-annulation of phthalides with a carbohydrate-derived optically active en
Autor:
Hiroto Kaku, Shinya Suzuki, Kei Kitamura, Makoto Inai, Mitsuyo Horikawa, Yuki Oguri, Tetsuto Tsunoda
Publikováno v:
Chemical and Pharmaceutical Bulletin. 68:380-383
The cryptolactones A1, A2, B1, and B2 isolated from a Cryptomyzus sp. aphid were synthesized via the Mukaiyama aldol reaction and olefin metathesis. Their antipodes and derivatives were also synthesized by the same strategy to investigate structure-a
Autor:
Makoto, Inai, Yuki, Oguri, Mitsuyo, Horikawa, Hiroto, Kaku, Shinya, Suzuki, Kei, Kitamura, Tetsuto, Tsunoda
Publikováno v:
Chemicalpharmaceutical bulletin. 68(4)
The cryptolactones A
Autor:
Takeshi Nishii, Yuki Takeuchi, Hiroto Kaku, Yuta Kawada, Mitsuyo Horikawa, Izumi Sakamoto, Takanori Naito, Kazuyoshi Makida, Tetsuto Tsunoda, Kazuya Iwaoka
Publikováno v:
Tetrahedron. 74:3052-3060
3,3-Dimethoxypropylsulfonyl (Dimps) chloride was prepared and used as a new versatile sulfonating agent for ammonia, primary and secondary amines to afford corresponding Dimps-amides in excellent yields. The resulting N-nonsubstituted and N-monosubst
Publikováno v:
Tetrahedron. 74:124-129
Racemic α-monosubstituted cyclopentanones were converted to optically active forms by a thermodynamically controlled deracemization using TADDOL-type host molecule 1 in alkaline aqueous MeOH. The efficiency of this conversion was strongly influenced
Publikováno v:
The Journal of antibiotics. 71(12)
Four red polyketide pigments, uroleuconaphins A1 (1) and B1 (2) and their glucosides 3 and 4, were isolated from the red goldenrod aphid Uroleucon nigrotuberculatum. Although these red pigments exist only as glucosides 3 and 4 in the intact insect bo
Autor:
Hiroto Kaku, Yuhei Sonoda, Mitsuyo Horikawa, Hideyuki Hishida, Yuri Taniguchi, Kei Kitamura, Takumi Hamaguchi, Akiko Kubo, Makoto Inai, Tetsuto Tsunoda
Publikováno v:
HETEROCYCLES. 98:1525