Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Kimio Uchida"'
Publikováno v:
Annals of Surgical Oncology. 24:1227-1233
Circulating tumor cells (CTCs) reportedly have been detected in the peripheral blood of more than 50% of breast carcinoma cases with distant metastases. Moreover, the survival period is shorter for patients who had more than five CTCs after a single
Publikováno v:
Chemical and Pharmaceutical Bulletin. 46:1034-1038
A short path synthesis of the ethyl (methyl 2, 3-O-isopropylidene-β-D-allofuranosid)uronate (5) and ethyl(methyl 2, 3-O-isopropylidene-α-L-talofuranosid)uronate (6) from methyl 2, 3-O-isopropylidene-β-D-ribopentodialdo-1, 4-furanoside (3) using (1
Publikováno v:
Tetrahedron: Asymmetry. 6:2131-2134
A highly stereoselective synthesis of the versatile chiral synthon possessing two stereogenic centers, (2S,3S)- 8 (>99% ee) was achieved and the conversion of (2S,3S)- 8 into the homochiral intermediate (2S,3S,4S)- 1 for the synthesis of nikkomycin B
Autor:
Minoru Endoh, S. G. Sankar, M. Hasegawa, Kimio Uchida, Masaaki Tokunaga, Yasuto Nozawa, Shigeho Tanigawa
Publikováno v:
Journal of Magnetism and Magnetic Materials. 124:325-329
Sm2Co17-type sintered magnets and Nd-Fe-B die-upset magnets have been investigated over the temperature range 4.2–423 K. Their magnetic properties were compared with those of SmCo5 and Nd-Fe-B sintered magnets. This study indicates that the Sm2Co17
Publikováno v:
ChemInform. 27
A highly stereoselective synthesis of the versatile chiral synthon possessing two stereogenic centers, (2S,3S)- 8 (>99% ee) was achieved and the conversion of (2S,3S)- 8 into the homochiral intermediate (2S,3S,4S)- 1 for the synthesis of nikkomycin B
Publikováno v:
ChemInform. 29
Publikováno v:
ChemInform. 29
A short path synthesis of the ethyl (methyl 2, 3-O-isopropylidene-β-D-allofuranosid)uronate (5) and ethyl(methyl 2, 3-O-isopropylidene-α-L-talofuranosid)uronate (6) from methyl 2, 3-O-isopropylidene-β-D-ribopentodialdo-1, 4-furanoside (3) using (1
Autor:
Yoshiaki Iwata, Kimio Uchida
Publikováno v:
TRANSACTIONS OF THE JAPAN SOCIETY OF MECHANICAL ENGINEERS Series C. 57:382-386
Publikováno v:
TRANSACTIONS OF THE JAPAN SOCIETY OF MECHANICAL ENGINEERS Series C. 57:521-526
Publikováno v:
HETEROCYCLES. 53:2253