K. Hattori

发表

896. EVOLUTION OF SOME LATE CRETACEOUS DESMOCERATINE AMMONOIDS

T. Okamoto, H. Hirano, K. Hattori, 1990 .

A new and facile route to spiro-ketal skeleton highly stereoselective CO bond formation by intramolecular Michael addition to δ,β-unsaturated sulfoxides

T. Imanishi, C. Iwata, S. Uchida, 1984 .

Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems--I. 2-Alkoxymethyl derivatives.

M. Murata, T. Kamimura, H. Azami, 1997, Bioorganic & medicinal chemistry.

Asymmetric induction by sulfinyl chirality: a total synthesis of (+)-talaromycin A and (−)-talaromycin B

T. Imanishi, Y. Moritani, M. Fujita, 1987 .

Synthetic studies on spiroketal natural products. IV: A stereoselective synthesis of (3S,5S,6R,9R,RS)-3-benzyloxymethyl-9-hydroxymethyl-5-(p-tolyl)sulfinyl-1,7-dioxaspiro[5.5]undecane, a key intermediate for talaromycins

T. Imanishi, Y. Moritani, Y. Takemoto, 1993 .

Asymmetric Induction by Sulfinyl Chirality. A Total Synthesis of (+)-Talaromycin A and (-)-Talaromycin B (I).

T. Imanishi, Y. Moritani, C. Iwata, 1987 .

Intramolecular michael addition reaction to chiral vinylic sulfoxides. An enantioselective synthesis of (R)- and (S)-1,7-dioxaspiro[5.5]undecane

T. Imanishi, M. Fujita, C. Iwata, 1985 .

Asymmetric functionalization at a prochiral carbon center by the aid of sulfinyl chirality: A selective formation of 6-substituted (3,S)- and (3,S)-3-hydroxymethyl-3,4-dihydro-5-(-tolyl)sulfinyl-2-pyrans

K. Sugiyama, T. Imanishi, Y. Moritani, 1987 .

Asymmetric Functionalization at a Prochiral Carbon Center by the Aid of Sulfinyl Chirality: A Selective Formation of 6‐Substituted (3R,Ss)and (3S,Ss)‐3‐Hydroxymethyl‐3,4‐dihydro‐5‐(p‐tolyl)sulfinyl‐2H‐pyrans.

T. Imanishi, Y. Moritani, K. Sugiyama, 1987 .