Y. Takayama

发表

Effect of Molecule–Electrode Contacts on Single-Molecule Conductivity of π-Conjugated System Measured by Scanning Tunneling Microscopy under Ultrahigh Vacuum

Masa-aki Suzuki, M. Fujihira, S. Fujii, 2006 .

Site-selective monotitanation of dialkynylpyridines and its application for preparation of highly fluorescent pi-conjugated oligomers.

Tomohiro Andou, Mizuki Takahashi, F. Sato, 2004, Organic letters.

One-pot synthesis of metalated pyridines from two acetylenes, a nitrile, and a titanium(II) alkoxide.

R. Tanaka, F. Sato, H. Urabe, 2005, Journal of the American Chemical Society.

Facile preparation of various heteroaromatic compounds via azatitanacyclopentadiene intermediates.

Y. Nobe, R. Tanaka, F. Sato, 2005, Journal of the American Chemical Society.

Synthesis of conjugated oligomers having aromatic and enediyne units alternately in the backbone that show intense fluorescence emission.

F. Sato, K. Ishizuka, Y. Takayama, 2004, Organic letters.

Site-selective iodine-magnesium exchange reaction of 1,4-diiodo-1,3-alkadienes by an organomagnesium ate complex, and its application to synthesis of polysubstituted styrenes and phenols.

F. Sato, Y. Takayama, K. Fukuhara, 2003, Journal of the American Chemical Society.

Efficient and practical method for synthesizing optically active indan-2-ols by the Ti(O-i-Pr)(4)/2 i-PrMgCl-mediated metalative Reppe reaction.

F. Sato, Y. Takayama, T. Hanazawa, 2003, The Journal of organic chemistry.

Development of a Chiral Propionaldehyde Homoenolate Equivalent Which Reacts with Imines with Excellent Stereoselectivity: Efficient and Practical Synthesis of Optically Active γ-Amino Carbonyl Compounds

X. Teng, F. Sato, Y. Takayama, 1999 .

Titanium(II)-Mediated Asymmetric Intramolecular Cyclization of 2,7- and 2,8-Enynyl Chiral Acetals. Synthetic Equivalent of Stoichiometric Intramolecular Asymmetric Metallo-Ene Reaction

S. Okamoto, F. Sato, Y. Takayama, 1999 .

Stereoselective synthesis of optically active substituted piperidines and pyrrolidines from amino acid derivatives by titanium(II)-mediated intramolecular cyclization reaction

S. Okamoto, F. Sato, Y. Takayama, 1997 .

Titanium(II)‐Mediated Intramolecular Cyclizations of 2, 7‐ and 2, 8‐Bis‐Unsaturated Carbonates and Acetates: A New and Efficient Synthesis of Cycloalkanes

Yuan Gao, F. Sato, Y. Takayama, 1997 .

Facile preparation of various heteroaromatic compounds via azatitanacyclopentadiene intermediates.

Y. Nobe, R. Tanaka, F. Sato, 2005, Journal of the American Chemical Society.

An efficient synthesis of optically active five- and six-membered cyclic compounds with selectable stereo-controls by a Ti(II)-mediated cyclization of chiral secondary 2,7- and 2,8-enyn-1-ol derivatives

Yongcheng Song, S. Okamoto, F. Sato, 2003 .

Titanium(II)‐Mediated Asymmetric Intramolecular Cyclization of 2,7‐ and 2,8‐Enynyl Chiral Acetals. Synthetic Equivalent of Stoichiometric Intramolecular Asymmetric Metallo‐Ene Reaction.

S. Okamoto, F. Sato, Y. Takayama, 1999 .

Development of a Chiral Propionaldehyde Homoenolate Equivalent Which Reacts with Imines with Excellent Stereoselectivity: Efficient and Practical Synthesis of Optically Active γ-Amino Carbonyl Compounds.

X. Teng, S. Okamoto, F. Sato, 2000 .

Asymmetric synthesis of stereodefined α-alkyl-γ-benzyloxymethyl-β-trimethylsilyl-γ-butyrolactones that serve as an efficient precursor for constructing carbon skeletons having a tertiary or quaternary stereogenic center

S. Okamoto, F. Sato, Kwangho Kim, 2002 .

Stereoselective Synthesis of Optically Active Substituted Piperidines and Pyrrolidines from Amino Acid Derivatives by Titanium(II)-Mediated Intramolecular Cyclization Reaction.

S. Okamoto, F. Sato, Y. Takayama, 1998 .

Efficient and Practical Method for Synthesizing Optically Active Indan‐2‐ols by the Ti(O‐iPr)4/2 iPrMgCl‐Mediated Metalative Reppe Reaction.

F. Sato, Y. Takayama, T. Hanazawa, 2003 .

Site-selective Pd-catalyzed coupling of 1,4-diiodo-1,3-alkadienes with Grignard reagents and its application to the synthesis of fulvenes.

F. Sato, Y. Takayama, M. Uemura, 2004, Organic letters.

Efficient and general synthetic method for preparing oligoenynes with either trans- or cis-olefinic configuration.

F. Sato, Y. Takayama, Kenji Muraoka, 2003, Organic letters.