Naohiro Aoyama

发表

Friedel–Crafts‐Type Conjugate Addition of Indoles Using a Lewis Acid–Surfactant‐Combined Catalyst in Water

Shuj Kobayashi, K. Manabe, Naohiro Aoyama, 2001 .

Design, synthesis, and evaluation of 4,6-diaminonicotinamide derivatives as novel and potent immunomodulators targeting JAK3.

Ayako Moritomo, Takayuki Inoue, M. Inami, 2016, Bioorganic & medicinal chemistry.

Stereodivergent catalytic doubly diastereoselective nitroaldol reactions using heterobimetallic complexes.

S. Matsunaga, M. Shibasaki, Y. Kato, 2008, Organic letters.

Allylation reactions of carbonyl compounds using an organosilicon reagent in aqueous media.

K. Manabe, T. Hamada, Naohiro Aoyama, 2003, Chemical communications.

Iron(III) Chloride as a Water-Compatible Lewis Acid for Diastereoselective Aldol Reactions in Water in the Presence of a Surfactant

K. Manabe, Naohiro Aoyama, S. Kobayashi, 2004 .

Dehydrative Glycosylation in Water Using a Bronsted Acid-Surfactant-Combined Catalyst

Naohiro Aoyama, S. Kobayashi, 2006 .

Ligand-accelerated cadmium-catalyzed asymmetric allylation reactions in aqueous media.

K. Manabe, Naohiro Aoyama, S. Kobayashi, 2003, Chirality.

Cross-coupling reactions of allylic alcohols in water

K. Manabe, Naohiro Aoyama, S. Kobayashi, 2005 .

Lanthanum aryloxide/pybox-catalyzed direct asymmetric Mannich-type reactions using a trichloromethyl ketone as a propionate equivalent donor.

S. Matsunaga, M. Shibasaki, G. Lu, 2007, Journal of the American Chemical Society.

Mechanistic studies on the catalytic cycle of metal fluoride-catalyzed allylation using allyltrimethoxysilane in protic solvents.

K. Manabe, T. Hamada, Naohiro Aoyama, 2003, The Journal of organic chemistry.

Ligand-Accelerated Cadmium-catalyzed Allylation of Aldehydes and Ketones in Aqueous Media

K. Manabe, Naohiro Aoyama, S. Kobayashi, 2002 .

Ba-Catalyzed Direct Mannich-Type Reactions of a β,γ-Unsaturated Ester Providing β-Methyl aza-Morita−Baylis−Hillman-Type Products

S. Matsunaga, M. Shibasaki, A. Yamaguchi, 2007 .

Design, synthesis, and pharmacological evaluation of N-(3-carbamoyl-1H-pyrazol-4-yl)-1,3-oxazole-4-carboxamide derivatives as interleukin-1 receptor-associated kinase 4 inhibitors with reduced potential for cytochrome P450 1A2 induction.

T. Kontani, E. Imamura, T. Ishikawa, 2023, Bioorganic & medicinal chemistry.