H. Uehara

发表

Anti-HIV-1 Antibodies and CD 4-IgG Breadth and Potency of Neutralization of Antibody Conjugation Approach Enhances

C. Barbas, D. Burton, M. Seaman, 2013 .

Antibody Conjugation Approach Enhances Breadth and Potency of Neutralization of Anti-HIV-1 Antibodies and CD4-IgG

C. Barbas, D. Burton, M. Seaman, 2013, Journal of Virology.

Total Synthesis of Ciguatoxin CTX3C

M. Satake, H. Oguri, M. Inoue, 2001, Science.

Potent Inhibition of HIV‐1 Entry with a Chemically Programmed Antibody Aided by an Efficient Organocatalytic Synthesis

C. Barbas, D. Burton, A. Hessell, 2010, Chembiochem : a European journal of chemical biology.

Total Synthesis of Ciguatoxin CTX3C

M. Satake, H. Oguri, M. Inoue, 2001, Science.

Synthesis-based approach toward direct sandwich immunoassay for ciguatoxin CTX3C.

H. Oguri, T. Tsumuraya, I. Fujii, 2003, Journal of the American Chemical Society.

Discovery of Lysine Hydroxylases in the Clavaminic Acid Synthase-Like Superfamily for Efficient Hydroxylysine Bioproduction

K. Kino, H. Kawabata, Ryoma Miyake, 2017, Applied and Environmental Microbiology.

One-pot enantioselective syntheses of iminosugar derivatives using organocatalytic anti-michael-anti-aza-Henry reactions.

C. Barbas, H. Uehara, Ritsuo Imashiro, 2010, Organic letters.

Organocatalytic asymmetric assembly reactions for the syntheses of carbohydrate derivatives by intermolecular Michael-Henry reactions

C. Barbas, Gloria Hernández-Torres, H. Uehara, 2010, Proceedings of the National Academy of Sciences.

Convergent synthesis of the EFGH ring fragment of ciguatoxin CTX3C

H. Oguri, M. Inoue, M. Hirama, 2001 .

The absolute configuration and total synthesis of korormicin

M. Hirama, T. Oishi, H. Uehara, 1999 .

anti-Selective asymmetric Michael reactions of aldehydes and nitroolefins catalyzed by a primary amine/thiourea.

C. Barbas, H. Uehara, 2009, Angewandte Chemie.

Convergent synthesis of the HIJKLM ring fragment of ciguatoxin CTX3C

M. Inoue, M. Hirama, T. Oishi, 2002 .

Organocatalytic enantioselective synthesis of nitrogen-substituted dihydropyran-2-ones, a key synthetic intermediate of 1beta-methylcarbapenems.

I. Ryu, Shoji Kobayashi, H. Uehara, 2009, Organic letters.

Practical total synthesis of ciguatoxin CTX3C by improved protective group strategy.

M. Inoue, M. Hirama, H. Uehara, 2002, Organic letters.

A concise route to the right wing of ciguatoxin

M. Inoue, A. Tatami, M. Hirama, 2003 .

Practical entry into the HIJKLM ring segment of ciguatoxin CTX3C

M. Hirama, T. Oishi, M. Shoji, 2001 .

CONVERGENT SYNTHESIS OF THE IJKLM RING FRAGMENT OF CIGUATOXIN CTX3C

M. Hirama, T. Oishi, M. Shoji, 1999 .

A CASE OF TOTAL DUPLICATION OF THE LARGE BOWEL WITH RECTAL CANCER IN AN ADULT PACIENT

H. Uehara, A. Kuroki, K. Kuroki, 1996 .

First- and second-generation total synthesis of ciguatoxin CTX3C.

M. Inoue, K. Miyazaki, M. Hirama, 2004, Proceedings of the National Academy of Sciences of the United States of America.

A new treatment for toxic megacolon

H. Uehara, A. Kuroki, Katsuro Knroki, 1998, The Lancet.