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書誌情報ファイル
Synthetic Approaches to Spiro-oxindoles and Iminoindolines Based on Formation of C2–C3 Bond
  Takemoto, Yoshiji; Tsukano, Chihiro (2014-09-25)
  HETEROCYCLES, 89(10): 2271-2302
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Electrophilic iodine(I) compounds induced semipinacol rearrangement via C-X bond cleavage.
  Tsuji, Nobuya; Kobayashi, Yusuke; Takemoto, Yoshiji (2014-09-16)
  Chemical communications, 50(89): 13691-13694
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Catalytic asymmetric synthesis of the pentacyclic core of (-)-nakadomarin A via oxazolidine as an iminium cation equivalent.
  Tsuji, Nobuya; Stadler, Michael; Kazumi, Naoya; Inokuma, Tsubasa; Kobayashi, Yusuke; Takemoto, Yoshiji (2014-08-27)
  Organic & biomolecular chemistry, 12(40): 7919-7922
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Synthesis of 3,3-Disubstituted 2-Aminoindolenines by Palladium-Catalyzed Allylic Amidination with Isocyanide
  Nanjo, Takeshi; Tsukano, Chihiro; Takemoto, Yoshiji (2014-06-04)
  Synlett, 25(10): 1473-1477
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Synthetic Study of Matrine-Type Alkaloids: Stereoselective Construction of the AB Rings of the Quinolizidine Skeleton
  Tsukano, Chihiro; Oimura, Atsuko; Enkhtaivan, Iderbat; Takemoto, Yoshiji (2014-03-05)
  Synlett, 25(5): 653-656
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Palladium(0)-Catalyzed Carbon[BOND]Hydrogen Bond Functionalization for the Synthesis of Indoloquinazolinones
  Tsukano, Chihiro; Okuno, Masataka; Nishiguchi, Hiromi; Takemoto, Yoshiji (2014-05-05)
  Advanced Synthesis & Catalysis, 356(7): 1533-1538
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Oxidant-Resistant Hydrogen-Bond-Donating Organocatalyst for Enantioselective Nucleophilic Epoxidation of α,β-Unsaturated Amides
  Kobayashi, Yusuke; Li, Shanji; Takemoto, Yoshiji (2014-04)
  Asian Journal of Organic Chemistry, 3(4): 403-407
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Synthesis of pyrrolophenanthridine alkaloids based on C(sp³)[BOND]H and C(sp²)[BOND]H functionalization reactions.
  Tsukano, Chihiro; Muto, Nobusuke; Enkhtaivan, Iderbat; Takemoto, Yoshiji (2014-09)
  Chemistry, an Asian journal, 9(9): 2628-2634
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Synthesis of 3,3-disubstituted indoline-2-thiones catalysed by an N-heterocyclic carbene.
  Ikota, Hideo; Ishida, Takayuki; Tsukano, Chihiro; Takemoto, Yoshiji (2014-06-16)
  Chemical communications, 50(64): 8871-8874
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