H. Houchigai

Highly diastereoselective Cu(I) catalyzed conjugate addition of grignard reagents to 2-cyclohexene-1,4-dione mono(ethylenethioacetal)

H. Takei, M. Asaoka, S. Sonoda, 1992 .

Synthesis and biological properties of a new series of anti-MRSA beta-lactams; 2-(thiazol-2-ylthio)carbapenems.

Y. Sumita, M. Sunagawa, H. Yamaga, 1997, Bioorganic & medicinal chemistry.

Synthesis and biological properties of a new series of anti-MRSA β-lactams; 2-(thiazol-2′-ylthio)carbapenems

Y. Sumita, M. Sunagawa, H. Yamaga, 1994 .

A highly regioselective reaction of allylic acetates with silylated carbon nucleophiles directed by a sulfenyl group

K. Kudo, K. Saigo, M. Hasegawa, 1991 .

A highly regioselective reaction of allylic acetates with silylated carbon nucleophiles directed by a sulfenyl group. Scope, limitation, and mechanistic aspects

K. Kudo, K. Saigo, M. Hasegawa, 1993 .

Highly Diastereoselective Cu(I)-Catalyzed Conjugate Addition of Grignard Reagents (II) to 2-Cyclohexene-1,4-dione Mono(ethylene Thioacetal) (I).

H. Takei, M. Asaoka, S. Sonoda, 1992 .

Synthesis and Biological Properties of a New Series of Anti‐MRSA β ‐Lactams; 2‐(Thiazol‐2′‐ylthio)carbapenems.

Y. Sumita, M. Sunagawa, H. Yamaga, 1995 .