スポンサーリンク
Department of Applied Chemistry, Faculty of Engineering, Tohoko University | 論文
- Lymphadenopathy of sinus histiocytosis mimicking metastatic bladder cancer : a case report
- The asymmetric Ullmann coupling reaction of chiral diol diesters of 1-bromo-2-naphthoic acid and 2-halo-3-nitrobenzoic acids: Highly diastereoselective synthesis of atropisomeric 6,6'-dinitrodiphenic acids.
- Carbon-carbon bond formation by use of chloroiodomethane as a C1 unit. I. Formation of chloromethyltriphenylphosphonium iodide, and its application for the Wittig chloromethylenation of aldehydes and ketones.
- Asymmetric synthesis of axially chiral, unsymmetrical diphenic acids via intramolecular Ullmann coupling reaction.
- The Ullmann coupling reaction of axially chiral (S)-2,2'-bis(1-iodo-2-naphthyloxycarbonyl)-1,1'-binaphthyl.
- Ultrasounds in synthetic reactions. II. Convenient methylenation of carbonyl compounds with zinc-diiodomethane.
- Base-catalyzed autoxidation of fluorene in the presence of phase transfer catalysts.
- The Reductive Coupling Reactions of Some Chloromethylbenzene Derivatives with Iron(II) and Copper(I) Complexes
- Ultrasounds in synthetic reactions. III. Reduction of organic halides with nickel(II) chloride-zinc-water.
- Palladium-catalyzed reaction of isoprene with water in presence of carbon dioxide and base.
- Axially dissymmetric bis(aminophosphine)s derived from 2,2'-diamino-1,1'-binaphthyl. Synthesis and application to rhodium(I)-catalyzed asymmetric hydrogenations.
- 2-Allylisourea as a starting material for palladium-catalyzed wittig-type allylidenation of aldehydes.
- The asymmetric Ullmann coupling reaction of (S)-2,2'-bis(1-bromo-2-naphthoyloxy)-1,1'-binaphthyl revisited. Formation of 24-membered optically pure cyclic dimer as well as 12-membered cyclic monomer.
- Reaction of dialkyl-substituted alkynes with carbon dioxide catalyzed by nickel(0) complexes. Incorporation of carbon dioxide in alkyne dimers and novel cyclotrimerization of the alkynes.
- Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. IV. The Mannich reaction of ketones by means of dihalomethane and secondary amine.
- Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. III. A convenient synthesis of the Mannich base from enol silyl ether by a combination of chloroiodomethane and N,N,N',N'-tetramethylmethanediamine.
- Direct N-allylation of amides with 2-allylisourea catalyzed by palladium(0).
- Selective oxidation of 2-bromo-m-xylene to 2-bromo-3-methylbenzoic acid or 2-bromoisophthalic acid.
- Reaction of allene with water catalyzed by palladium(0) in the presence of carbon dioxide.
- Carbon-carbon bond formation by the use of chloroiodomethane as a C1 unit. II. The preparation and synthetic application of 1-chloro-3-iodoheptane.
スポンサーリンク