关注
Hikaru Fujita
Hikaru Fujita
在 staff.kanazawa-u.ac.jp 的电子邮件经过验证
标题
引用次数
引用次数
年份
A Novel Acid-Catalyzed O-Benzylating Reagent with the Smallest Unit of Imidate Structure
K Yamada, H Fujita, M Kunishima
Organic letters 14 (19), 5026-5029, 2012
1022012
A practical method for p-methoxybenzylation of hydroxy groups using 2, 4, 6-tris (p-methoxybenzyloxy)-1, 3, 5-triazine (TriBOT-PM)
K Yamada, H Fujita, M Kitamura, M Kunishima
Synthesis 45 (21), 2989-2997, 2013
502013
Study of the reactivities of acid-catalyzed O-benzylating reagents based on structural isomers of 1, 3, 5-triazine
H Fujita, N Hayakawa, M Kunishima
The Journal of Organic Chemistry 80 (21), 11200-11205, 2015
272015
O‐Benzylation of Carboxylic Acids Using 2,4,6‐Tris(benzyloxy)‐1,3,5‐triazine (TriBOT) under Acidic or Thermal Conditions
K Yamada, S Yoshida, H Fujita, M Kitamura, M Kunishima
European Journal of Organic Chemistry 2015 (36), 7997-8002, 2015
252015
Design, synthesis, and utility of defined molecular scaffolds
D Sato, Z Wu, H Fujita, JS Lindsey
Organics 2 (3), 161-273, 2021
232021
Annulated bacteriochlorins for near-infrared photophysical studies
H Fujita, H Jing, M Krayer, S Allu, G Veeraraghavaiah, Z Wu, J Jiang, ...
New Journal of Chemistry 43 (19), 7209-7232, 2019
212019
Bacteriochlorin‐bis (spermine) conjugate affords an effective photodynamic action to eradicate microorganisms
MB Ballatore, ME Milanesio, H Fujita, JS Lindsey, EN Durantini
Journal of Biophotonics 13 (2), e201960061, 2020
202020
2-[18F] Fluorophenylalanine: Synthesis by nucleophilic 18F-fluorination and preliminary biological evaluation
DJ Modemann, BD Zlatopolskiy, EA Urusova, J Zischler, A Craig, J Ermert, ...
Synthesis 51 (03), 664-676, 2019
172019
N, N′‐Dimethylated Benzyloxytriazinedione: A Stable Solid Reagent for Acid‐Catalyzed O‐Benzylation
H Fujita, S Kakuyama, M Kunishima
European Journal of Organic Chemistry 2017 (4), 833-839, 2017
172017
Development of a Triazine‐Based tert‐Butylating Reagent, TriAT‐tBu
K Yamada, N Hayakawa, H Fujita, M Kitamura, M Kunishima
European Journal of Organic Chemistry 2016 (23), 4093-4098, 2016
152016
Development of acid-catalyzed fluorous benzylating reagents based on a triazinedione core
M Kunishima, R Asao, K Yamada, M Kitamura, H Fujita
Journal of Fluorine Chemistry 190, 68-74, 2016
142016
Chromogenic agents built around a multifunctional double-triazine framework for enzymatically triggered cross-linking under physiological conditions
H Fujita, Y Zhang, Z Wu, JS Lindsey
New Journal of Chemistry 44 (10), 3856-3867, 2020
132020
A Simple Method for the Preparation of Stainless and Highly Pure Trichloroacetimidates
K Ikeuchi, K Murasawa, H Yamada
Synlett 30 (11), 1308-1312, 2019
132019
Study of O-Allylation Using Triazine-Based Reagents
K Yamada, N Hayakawa, H Fujita, M Kitamura, M Kunishima
Chemical and Pharmaceutical Bulletin 65 (1), 112-115, 2017
132017
Enzymatically triggered chromogenic cross-linking agents under physiological conditions
H Fujita, J Dou, N Matsumoto, Z Wu, JS Lindsey
New Journal of Chemistry 44 (3), 719-743, 2020
122020
Substitution of the Dimethylamino Group in Gramines and One-Pot Cyclization to Tetrahydro-β-carbolines Using a Triazine-Based Activating Agent
H Fujita, R Nishikawa, O Sasamoto, M Kitamura, M Kunishima
The Journal of Organic Chemistry 84 (13), 8380-8391, 2019
122019
Triazine-Based Cationic Leaving Group: Synergistic Driving Forces for Rapid Formation of Carbocation Species
H Fujita, S Kakuyama, S Fukuyoshi, N Hayakawa, A Oda, M Kunishima
The Journal of Organic Chemistry 83 (8), 4568-4580, 2018
112018
Development of triazinone-based condensing reagents for amide formation
K Yamada, M Kota, K Takahashi, H Fujita, M Kitamura, M Kunishima
The Journal of Organic Chemistry 84 (23), 15042-15051, 2019
102019
Development of highly electron-deficient and less sterically-hindered phosphine ligands possessing 1, 3, 5-triazinyl groups
K Abe, M Kitamura, H Fujita, M Kunishima
Molecular Catalysis 445, 87-93, 2018
102018
New molecular design for blue BODIPYs
Z Wu, H Fujita, NCM Magdaong, JR Diers, D Hood, S Allu, ...
New Journal of Chemistry 43 (19), 7233-7242, 2019
92019
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