2000
Structure
and stereochemistry of nardostachysin, a new terpenoid
ester constituent of the rhizomes of nardostachys
jatamansi. Chatterjee,
A.; Basak, B.; Saha, M.; Dutta, U.; Mukhopadhyay, C.;
Banerji, J.; Konda, Y.; Harigaya,
Y.
Journal of Natural Products, 63(11), 1531-1533,
2000.
Synthetic
conversion of ACAT inhibitor to acetylcholinesterase
inhibitor. Obata,
R.; Sunazuka, T.; Otoguro, K.; Tomoda, H.;
Harigaya,
Y.;
Ōmura, S. Bioorganic & Medicinal Chemistry Letters,
10(12), 1315-1316,
2000.
Synthesis
and antiangiogenic activity of staurosporine
derivatives. Li, Z.;
Sunazuka, T.; Yamada, R.; Kato, Y.; Enomoto, A.; Hayashi,
M.; Harigaya,
Y.;
Ōmura, S. Journal of Antibiotics, 53(4), 426-429,
2000.
Structure-activity
relationships study of pyripyropenes: reversal of cancer
cell multidrug resistance. Obata,
R.; Sunazuka, T.; Harigaya,
Y.; Rho,
M-C.; Tomoda, H.; Ōmura, S. Journal of Antibiotics, 53(4),
422-425,
2000.
Total
syntheses of kurasoin A and B, novel protein
farnesyltransferase inhibitors, and absolute structures of
kurasoin A and B. Hirose,
T.; Sunazuka, T.; Zhi-Ming, T.; Handa, M.; Uchida, R.;
Shiomi, K.; Harigaya,
Y.;
Ōmura, S. Heterocycles, 53(4), 777-784,
2000.
Neat
formic acid: an excellent N-formylating agent for
carbazoles, 3-alkylindoles, diphenylamine and moderately
weak nucleophilic anilines. Chakrabarty,
M.; Khasnobis, S.; Harigaya,
Y.;
Konda, Y. Synthetic Communications, 30(2), 187-200,
2000.
Total
synthesis of (+)-madindoline A and (-)-madindoline B,
potent, selective inhibitors of interleukin 6.
Determination of the relative and absolute
configurations. Sunazuka,
T.; Hirose, T.; Shirahata, T.; Harigaya,
Y.;
Hayashi, M..; Komiyama, K.; Ōmura, S.; Smith, Amos B., III.
Journal of the American Chemical Society, 122(9),
2122-2123,
2000.
Analysis
of ballpoint pen inks by field desorption mass
spectrometry. Sakayanagi,
M.; Komuro, J.; Konda, Y.; Watanabe, K.;
Harigaya, Y.
Journal of Forensic Sciences, 44(6), 1204-1214,
2000.