N. Ikemoto

发表

Feng Xu, Edward J. J. Grabowski, Shane W. Krska, 2009 .

Highly efficient asymmetric synthesis of sitagliptin.

Feng Xu, Andrew Clausen, Shane W. Krska, 2009, Journal of the American Chemical Society.

Calicheamicin-DNA complexes: warhead alignment and saccharide recognition of the minor groove.

D. Patel, S. Danishefsky, G. Ellestad, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Highly diastereoselective heterogeneously catalyzed hydrogenation of enamines for the synthesis of chiral beta-amino acid derivatives.

E. Njolito, D. Tellers, J. Armstrong, 2004, Journal of the American Chemical Society.

Chromatography as an Enabling Technology in Pharmaceutical Process Development: Expedited Multikilogram Preparation of a Candidate HIV Protease Inhibitor

C. Welch, F. Antia, J. Armstrong, 2004 .

Asymmetric direduction of 1,2-indanedione to cis (1S,2R) indanediol by Trichosporon cutaneum MY 1506.

M. Chartrain, R. Greasham, N. Ikemoto, 1999, Journal of bioscience and bioengineering.

Solution structure of the calicheamicin gamma 1I-DNA complex.

D. Patel, R. A. Kumar, N. Ikemoto, 1997, Journal of molecular biology.

Efficient synthesis of the optically active dihydropyrimidinone of a potent α1A- selective adrenoceptor antagonist

M. Chartrain, E. Hu, D. Sidler, 2002 .

Solution structure of the esperamicin A1-DNA complex.

D. Patel, D J Patel, R A Kumar, 1997, Journal of molecular biology.

Discovery and synthesis of HIV integrase inhibitors: development of potent and orally bioavailable N-methyl pyrimidones.

Michael Rowley, Cristina Gardelli, Marco Ferrara, 2007, Journal of medicinal chemistry.

Ferric chloride, an anomerization catalyst for the preparation of alkyl α-glycopyranosides

K. Nakanishi, L. Lo, Mayland Chang, 1992 .

Total synthesis of (-)-hikizimycin employing the strategy of two-directional chain synthesis

S. Schreiber, N. Ikemoto, 1992 .

Total synthesis of the anthelmintic agent hikizimycin

S. Schreiber, N. Ikemoto, 1990 .

Practical routes to the triarylsulfonyl chloride intermediate of a β3 adrenergic receptor agonist

P. Reider, Jinchu Liu, J. Mcnamara, 2003 .

Highly selective synthesis of 2-substituted-5-hydroxy-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid derivatives using a novel protected dihydroxyfumarate

J. Armstrong, D. Mathre, T. Novak, 2004 .

Synthesis of chemically reactive analogues of AZT and their biological evaluation against HIV

S. Schreiber, N. Ikemoto, 1988 .

Approaches to installing a N-gem-dimethylmethylene-2-oxazolyl group and application to the synthesis of a second generation HIV protease inhibitor

J. Armstrong, Ross A. Miller, F. Fleitz, 2005 .

Asymmetric hydrogenation of N-sulfonylated-alpha-dehydroamino acids: toward the synthesis of an anthrax lethal factor inhibitor.

Yong-kui Sun, E. Grabowski, S. Krska, 2005, Organic letters.

Total synthesis of a second generation HIV protease inhibitor

J. Armstrong, F. Fleitz, R. Volante, 2003 .

Adsorption of hydrogen and deuterium on A-type zeolites at 77 K after various heat treatments

M. Hara, K. Yonehara, N. Ikemoto, 2020 .

CD Exciton Chirality Method: Schiff Base and Cyanine Dye‐Type Chromophores for Primary Amino Groups.

K. Nakanishi, N. Berova, T. Iwashita, 1994 .

X-ray structure of methyl 1,6-di-O-(4-bromobenzoyl)-3,4-di-O-(4-methoxycinnamoyl)-β-d-fructofuranoside

G. Schulte, N. Ikemoto, 1994 .

Detection of Subpicomole Levels of Compounds Containing Hydroxyl and Amino Groups with the Fluorogenic Reagent, 2-Naphthoylimidazole""

K. Nakanishi, L. Lo, N. Ikemoto, 1992 .

Oligosaccharide microscale analysis by circular dichroic spectroscopy: reference spectra for chromophoric D-fructofuranoside derivatives.

K. Nakanishi, N. Berova, L. Lo, 1993, Carbohydrate research.

Production of cis-1,2-dihydroxy-3-methylcyclohexa-3,5-diene (toluene cis glycol) by Rhodococcus sp. MA 7249.

M. Chartrain, B. Buckland, R. Greasham, 2000, Journal of bioscience and bioengineering.

Atmospheric Concentration and Deposition Flux of Cosmogenic Beryllium-7 at Toki, Central Part of Japan

Masahiro Tanaka, T. Kovács, H. Kakiuchi, 2018 .

Tritium Concentration of Inland Water in Okinawa Island, Southwestern Part of Japan

Masahiro Tanaka, N. Akata, M. Furukawa, 2018 .

CD exciton chirality method : new chromophores for primary amino groups

K. Nakanishi, N. Berova, J. Odingo, 1993 .

Activated Carbon Impregnated with Elementary Iodine: Applications against Virus- and Bacteria-Related Issues

K. Otsuki, F. Spaziani, H. Takakuwa, 2021, C++ Conference.

Efficient preparation of chiral diamines via Red-Al reduction of N-Boc-protected amino acid-derived secondary amides

E. Voight, M. H. Kress, N. Ikemoto, 2006 .

CD EXCITON CHIRALITY METHOD : SCHIFF BASE AND CYANINE DYE-TYPE CHROMOPHORES FOR PRIMARY AMINO GROUPS

K. Nakanishi, N. Berova, T. Iwashita, 1994 .

Improving the in vivo therapeutic index of siRNA polymer conjugates through increasing pH responsiveness.

L. Sepp-Lorenzino, I. Davies, B. Howell, 2014, Bioconjugate chemistry.

Process Development of a Potent Bradykinin 1 Antagonist

Fouzia Machrouhi, D. Frantz, Cameron J. Cowden, 2009 .

Synthesis and a Preliminary DNA Binding Study of Hybrids of the Carbohydrate Domain of Calicheamicin γ 1I and the Aglycone of Daunorubicin: Calichearubicins A and B

D. Crothers, S. Danishefsky, K. Depew, 1996 .

Improved syntheses of α-BOC-aminoketones from α-BOC-amino-Weinreb amides using a pre-deprotonation protocol

J. Armstrong, Jinchu Liu, N. Ikemoto, 2002 .

Efficient Preparation of Chiral Diamines via Red‐Al Reduction of N‐Boc‐Protected Amino Acid‐Derived Secondary Amides.

E. Voight, M. H. Kress, N. Ikemoto, 2006 .