T. Yasukata

发表

Antibacterial oxazolidinone analogues having a N-hydroxyacetyl-substituted seven-membered [1,2,5]triazepane or [1,2,5]oxadiazepane C-ring unit.

K. Shudo, T. Iwaki, Hideyuki Suzuki, 2013, European journal of medicinal chemistry.

Novel semi-synthetic glycopeptide antibiotics active against methicillin-resistant staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci (VRE): doubly-modified water-soluble derivatives of chloroorienticin B.

T. Yasukata, Tadashi Munekage, Y. Sumino, 2002, Bioorganic & medicinal chemistry letters.

A new type of ketolides bearing an N-aryl-alkyl acetamide moiety at the C-9 iminoether synthesis and structure-activity relationships.

T. Iwaki, T. Yasukata, Takashi Nomura, 2005, Bioorganic & medicinal chemistry.

Practical Synthesis of Ethyl 1-(tert-Butoxycarbonyl)-4-(1-pyrrolidinyl)-4-piperidineacetate, an Intermediate of a Novel Antiarteriosclerotic, Utilizing Aza-Michael Addition Promoted by LiBr

A. Iida, T. Yasukata, Naohiro Onodera, 2012 .

A novel series of parenteral cephalosporins exhibiting potent activities against both Pseudomonas aeruginosa and other gram-negative pathogens. Part 2: Synthesis and structure-activity relationships.

K. Takeda, T. Yasukata, Y. Yamano, 2007, Bioorganic & medicinal chemistry.

A mild method for the synthesis of carbamate-protected guanidines using the Burgess reagent.

T. Yasukata, T. Maki, T. Tsuritani, 2014, Organic letters.

A catalytic asymmetric Wagner-Meerwein shift.

B. Trost, T. Yasukata, Tatsuro Yasukata, 2001, Journal of the American Chemical Society.

An efficient and practical method for solid-phase synthesis of tripeptide-bearing glycopeptide antibiotics: combinatorial parallel synthesis of carboxamide derivatives of chloroorienticin B.

T. Yasukata, Tadashi Munekage, Y. Sumino, 2002, Bioorganic & medicinal chemistry letters.

Enantioselective protonation of achiral lithium enolates using a chiral amine in the presence of lithium bromide

K. Koga, T. Yasukata, 1993 .

Synthesis and in vitro/in vivo antibacterial activity of oxazolidinones having thiocarbamate at C-5 on the A-ring and an amide- or urea-substituted [1,2,5]triazepane or [1,2,5]oxadiazepane as the C-ring.

K. Shudo, T. Iwaki, Hideyuki Suzuki, 2013, European journal of medicinal chemistry.

9-Oxime-3-ketolides: modification at the C-11,12-diol moiety and antibacterial activities against key respiratory pathogens.

T. Yasukata, Takashi Nomura, Y. Narukawa, 2005, Bioorganic & medicinal chemistry.

An unusual regioselectivity in the Pd-catalyzed cross coupling of alkynes. A correction

B. Trost, J. Gunzner, T. Yasukata, 2001 .

An Unusual Regioselectivity in the Pd‐Catalyzed Cross Coupling of Alkynes. A Correction.

B. Trost, J. Gunzner, T. Yasukata, 2001 .

Stereoselective Reactions. XXII. Design and Synthesis of Chiral Chelated Lithium Amides for Enantioselective Reactions

R. Shirai, K. Koga, K. Aoki, 1994 .

Practical Synthetic Method for the Preparation of Pyrone Diesters: An Efficient Synthetic Route for the Synthesis of Dolutegravir Sodium

M. Nagai, T. Yasukata, K. Okamoto, 2019, Organic Process Research & Development.

Practical and Scalable Synthetic Method for Preparation of Dolutegravir Sodium: Improvement of a Synthetic Route for Large-Scale Synthesis

Y. Aoyama, M. Nagai, T. Yasukata, 2019, Organic Process Research & Development.