H. Usuda

发表

The first catalytic asymmetric total synthesis of ent-hyperforin

M. Kanai, M. Shibasaki, Shi‐Liang Shi, 2010 .

Catalytic asymmetric total synthesis of ent-hyperforin.

M. Kanai, M. Shibasaki, Shi‐Liang Shi, 2010, Angewandte Chemie.

A new approach for the construction of a highly congested bicyclic system in polycyclic polyprenylated acylphloroglucinols (PPAPs)

M. Kanai, M. Shibasaki, Yohei Shimizu, 2007 .

Synthesis and evaluation of novel 1H-pyrrolo[2,3-b]pyridine-5-carboxamide derivatives as potent and orally efficacious immunomodulators targeting JAK3.

A. Tanaka, K. Nakai, Ayako Moritomo, 2015, Bioorganic & medicinal chemistry.

Studies toward the total synthesis of garsubellin A: a concise synthesis of the 18-epi-tricyclic core.

M. Kanai, M. Shibasaki, H. Usuda, 2002, Organic letters.

A Catalytic Asymmetric Strecker‐Type Reaction: Interesting Reactivity Difference between TMSCN and HCN

M. Kanai, Y. Hamashima, M. Shibasaki, 2000 .

Catalytic enantioselective Strecker reaction of ketoimines.

Masato Suzuki, M. Kanai, M. Shibasaki, 2003, Journal of the American Chemical Society.

Catalytic enantioselective Strecker reaction of ketoimines.

Masato Suzuki, M. Kanai, M. Shibasaki, 2003, Journal of the American Chemical Society.

A Catalytic Asymmetric Strecker-Type Reaction: Interesting Reactivity Difference Between Tms-CN and HCN.

M. Kanai, Y. Hamashima, M. Shibasaki, 2000 .

Challenge toward structural complexity using asymmetric catalysis: target-oriented development of catalytic enantioselective Diels-Alder reaction.

M. Kanai, M. Shibasaki, H. Usuda, 2004, Organic letters.

Studies toward the total synthesis of garsubellin A: synthesis of 8-deprenyl-garsubellin A

M. Kanai, M. Shibasaki, H. Usuda, 2002 .

A catalytic asymmetric strecker-type reaction promoted by Lewis acid-Lewis base bifunctional catalyst.

M. Kanai, Y. Hamashima, M. Shibasaki, 2000, Chemical & pharmaceutical bulletin.

Discovery of tricyclic dipyrrolopyridine derivatives as novel JAK inhibitors.

Ayako Moritomo, Takayuki Inoue, M. Inami, 2017, Bioorganic & medicinal chemistry.

Design, synthesis, and pharmacological evaluation of N-(3-carbamoyl-1H-pyrazol-4-yl)-1,3-oxazole-4-carboxamide derivatives as interleukin-1 receptor-associated kinase 4 inhibitors with reduced potential for cytochrome P450 1A2 induction.

T. Kontani, E. Imamura, T. Ishikawa, 2023, Bioorganic & medicinal chemistry.