H. Jona

发表

Asymmetric synthesis of a selective endothelin A receptor antagonist.

K. Tomimoto, T. Mase, Y. Tsuchiya, 2002, Chemical & pharmaceutical bulletin.

Convergent Total Syntheses of Oligosaccharides by One-Pot Sequential Stereoselective Glycosylations

T. Mukaiyama, T. Hashihayata, Kazuya Takeuchi, 2003 .

Protic Acid Catalyzed Stereoselective Glycosylation Using Glycosyl Fluorides.

W. Chavasiri, Hiroki Mandai, T. Mukaiyama, 2002 .

A Novel Activating Agents of ‘Disarmed’ Thioglycosides, Combination of Trityl Tetrakis(pentafluorophenyl)borate, Iodine and 2,3-Dichloro-5,6-dicyano-p-benzoquinone (DDQ)

T. Mukaiyama, Kazuya Takeuchi, H. Jona, 2000 .

A Novel Method for the Synthesis of Thiols from the Corresponding Olefins by Using Thiocarbonates and Ti(IV) Halides

T. Mukaiyama, Terunobu Saitoh, H. Jona, 2001 .

A Catalytic and α-Selective Sialylation Using Novel 5-Azido Sialyl Fluoride

Hiroki Mandai, T. Mukaiyama, H. Jona, 2002 .

Catalytic and Stereoselective Glycosylation with Disarmed Glycosyl Fluoride Having Phthaloyl or Dichlorophthaloyl Protected Amino Function Using a 1 : 2 Combination of Stannic Chloride and Silver Tetrakis(pentafluorophenyl)borate

T. Mukaiyama, H. Jona, H. Maeshima, 2001 .

Catalytic and Stereoselective Glycosylation with Disarmed Glycosyl Fluoride by Using a Combination of Stannous(II) Chloride (SnCl2) and Silver Tetrakis(pentafluorophenyl)borate [AgB(C6F5)4] as a Catalyst

T. Mukaiyama, H. Jona, H. Maeshima, 2001 .

A Catalytic and Stereoselective Glycosylation with Glucopyranosyl Fluoride by Using Various Protic Acids

Hiroki Mandai, T. Mukaiyama, H. Jona, 2001 .

SYNTHESIS OF DISSYMMETRIC INDOLOCARBAZOLE GLYCOSIDES USING THE MITSUNOBU REACTION AT THE GLYCOSYLATION STEP

T. Honma, S. Ito, T. Nishimura, 1997 .

Efficient and practical asymmetric synthesis of 1-tert-butyl 3-methyl (3R,4R)-4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidine-1,3-dicarboxylate, a useful intermediate for the synthesis of nociceptin antagonists

Y. Iwasawa, J. Shibata, H. Kawamoto, 2009 .

Novel dithiocarbamate carbapenems with anti-MRSA activity.

H. Satō, N. Ohtake, M. Moriya, 1997, Bioorganic & medicinal chemistry.

Structure–activity relationships of trans-3,5-disubstituted pyrrolidinylthio-1β-methylcarbapenems. Part 1: J-111,347 and related compounds

Hiroki Sato, H. Morishima, N. Ohtake, 2000 .

Practical synthesis of indolopyrrolocarbazoles

T. Honma, T. Nishimura, M. Ohkubo, 1996 .

Synthetic study toward vineomycins. Synthesis of c-aryl glycoside sector via Cp2HfCl2AgClO4-promoted tactics

Takashi Matsumoto, Keisuke Suzuki, H. Jona, 1989 .

Convergent and Convenient Total Synthesis of Phytoalexin-Elicitor Active Heptasaccharide by One-Pot Sequential Glycosylation

T. Mukaiyama, T. Hashihayata, H. Jona, 2002 .

A Convergent Total Synthesis of the Mucin Related F1α Antigen by One-Pot Sequential Stereoselective Glycosylation

T. Mukaiyama, T. Hashihayata, Kazuya Takeuchi, 2001 .

Diastereoselective synthesis of the key intermediate of the BO-2727 side chain

N. Ohtake, O. Okamoto, H. Jona, 1997 .

A Catalytic and Stereoselective Glycosylation withβ-Glycosyl Fluorides

T. Mukaiyama, Terunobu Saitoh, Kazuya Takeuchi, 2000 .

Highly α-Selective Glycosylation with Glycopyranosyl Fluorides Having Diethylthiocarbamoyl Group

T. Mukaiyama, H. Jona, H. Chiba, 2002 .

1,2-Cis Selective Glycosylation with Glycosyl Fluoride by Using a Catalytic Amount of Trifluoromethanesulfonic Acid (TfOH) in the Coexistence of Molecular Sieve 5Å (MS5Å)

T. Mukaiyama, Kazuya Takeuchi, H. Jona, 2000 .

1,2-cis Selective Glycosylation with Glycosyl Fluoride by Using a Catalytic Amount of Trifluoromethanesulfonic Acid (TfOH) in the Coexistence of Molecular Sieve 5Å (MS5Å).

T. Mukaiyama, Kazuya Takeuchi, H. Jona, 2001 .

Convergent total synthesis of vineomycinone B2 methyl ester and its C(12)-epimer

Takashi Matsumoto, Keisuke Suzuki, H. Jona, 1991 .

Potent and orally active ET(A) selective antagonists with 5,7-diarylcyclopenteno[1,2-b]pyridine-6-carboxylic acid structures.

T. Hayama, S. Ozaki, Y. Shibata, 2004, Bioorganic & medicinal chemistry.

Efficient method for introducing vineomycin-fridamycin-type side chain. Total synthesis of fridamycin E

Takashi Matsumoto, Keisuke Suzuki, H. Jona, 1991 .

Highly α-Selective Glycosylation with Glycopyranosyl Fluorides Having Diethylthiocarbamoyl Group.

T. Mukaiyama, H. Jona, H. Chiba, 2002 .

Dicationic dithiocarbamate carbapenems with anti-MRSA activity.

H. Morishima, N. Ohtake, Y. Sugimoto, 2001, Bioorganic & medicinal chemistry.