M. Ikunaka

发表

Microbial Hydroxylation of Indole to 7-Hydroxyindole by Acinetobacter calcoaceticus Strain 4-1-5

M. Kubo, T. Sekiguchi, D. Sugimori, 2004, Bioscience, biotechnology, and biochemistry.

A scalable synthesis of (R)-3-(2-aminopropyl)-7-benzyloxyindole via resolution

S. Kato, H. Harada, M. Ikunaka, 2001 .

Bacillus subtilis epoxide hydrolase-catalyzed preparation of enantiopure 2-methylpropane-1,2,3-triol monobenzyl ether and its application to expeditious synthesis of (R)-bicalutamide

T. Sugai, R. Obata, S. Nishiyama, 2007 .

Synthetic studies on novel 1,4-dihydro-2-methylthio-4,4,6-trisubstituted pyrimidine-5-carboxylic acid esters and their tautomers.

Y. Okamoto, M. Ikunaka, Y. Ohyama, 2011, Chemical & pharmaceutical bulletin.

Asymmetric Phase‐Transfer Catalysis for the Production of Non‐Proteinogenic α‐Amino Acids

K. Maruoka, M. Ikunaka, 2010 .

PTC in OPRD: An Illustrative Overview

M. Ikunaka, 2008 .

Stereoselective synthesis of a novel 2-aza-7-oxabicyclo[3.3.0]octane as neurokinin-1 receptor antagonist.

F. Ito, Y. Shishido, M. Ikunaka, 2007, Bioorganic & medicinal chemistry letters.

Catalytic Asymmetric Carbon−Carbon Bond Formations: Their Evolution from Biocatalysis to Organocatalysis over the Millennium

M. Ikunaka, 2007 .

Process development with Bifunctional chiral epoxides to access single enantiomrs of pharmaceutical intermediates

T. Sugai, M. Ikunaka, 2008 .

A concise synthesis of (2S, 3S)-BocAHPBA and (R)-BocDMTA, chiral building blocks for peptide-mimetic HIV protease inhibitors

J. Matsumoto, M. Ikunaka, Y. Nishimoto, 2002 .

A Scalable Synthesis of (R)-3,5-Dihydro-4H-dinaphth[2,1-c:1‘2‘-e]azepine

K. Maruoka, T. Ooi, M. Ikunaka, 2003 .

Synthesis of all of the four energetically possible stereoisomers of 7-ethyl-2-methyl-1,6-dioxaspiro[4.5]decane: A pheromone produced by bees Paravespura vulgaris l. and Andrena haemorrhoa F.

K. Mori, M. Ikunaka, 1984 .

There's No Industrial Biocatalyst Like Hydrolase: Development of Scalable Enantioselective Processes Using Hydrolytic Enzymes1

F. Nomoto, K. Ogawa, Y. Chikusa, 2003 .

An Expeditious Scalable Synthesis of (S)-2-Amino-5-methoxytetralin via Resolution

J. Matsumoto, M. Ikunaka, Y. Hirayama, 2005 .

A practical enantioselective synthesis of (S)-3-hydroxytetradecanoic acid

M. Ikunaka, K. Matsuyama, 1999 .

A scalable chemoenzymatic preparation of (R)-tetrahydrofuran-2-carboxylic acid

M. Ikunaka, Y. Fujima, Y. Nishimoto, 2003 .

A practical chemoenzymatic process to access (R)-quinuclidin-3-ol on scale

F. Nomoto, M. Ikunaka, Toru Inoue, 2003 .

Synthesis of (-)-talaromycins a and b

K. Mori, M. Ikunaka, 1987 .

A process in need is a process indeed: scalable enantioselective synthesis of chiral compounds for the pharmaceutical industry.

M. Ikunaka, 2003, Chemistry.

Optical Rotatory Dispersion of Spiroacetals

K. Mori, M. Ikunaka, 1987 .

A Practical RuCl3-Catalyzed Oxidation Using Trichloroisocyanuric Acid As a Stoichiometric Oxidant under Mild Nonacidic Conditions

M. Ikunaka, N. Moriya, H. Yamaoka, 2004 .