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Naoko Ichiishi
Naoko Ichiishi
Sanofi
Adresse e-mail validée de umich.edu
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Late-stage [18 F] fluorination: new solutions to old problems
AF Brooks, JJ Topczewski, N Ichiishi, MS Sanford, PJH Scott
Chemical science 5 (12), 4545-4553, 2014
3132014
Copper-Catalyzed [18F]Fluorination of (Mesityl)(aryl)iodonium Salts
N Ichiishi, AF Brooks, JJ Topczewski, ME Rodnick, MS Sanford, PJH Scott
Organic letters 16 (12), 3224-3227, 2014
2582014
Synthesis of [18F]Arenes via the Copper-Mediated [18F]Fluorination of Boronic Acids
AV Mossine, AF Brooks, KJ Makaravage, JM Miller, N Ichiishi, MS Sanford, ...
Organic letters 17 (23), 5780-5783, 2015
2432015
Cu-catalyzed fluorination of diaryliodonium salts with KF
N Ichiishi, AJ Canty, BF Yates, MS Sanford
Organic letters 15 (19), 5134-5137, 2013
1972013
Palladium-and nickel-catalyzed decarbonylative C–S coupling to convert thioesters to thioethers
N Ichiishi, CA Malapit, Ł Woźniak, MS Sanford
Organic letters 20 (1), 44-47, 2018
1222018
Protecting group free radical C–H trifluoromethylation of peptides
N Ichiishi, JP Caldwell, M Lin, W Zhong, X Zhu, E Streckfuss, HY Kim, ...
Chemical science 9 (17), 4168-4175, 2018
1022018
Pd-catalyzed decarbonylative cross-couplings of aroyl chlorides
CA Malapit, N Ichiishi, MS Sanford
Organic letters 19 (15), 4142-4145, 2017
902017
Mechanistic Investigations of Cu-Catalyzed Fluorination of Diaryliodonium Salts: Elaborating the CuI/CuIII Manifold in Copper Catalysis
N Ichiishi, AJ Canty, BF Yates, MS Sanford
Organometallics 33 (19), 5525-5534, 2014
742014
Development of Customized [18F]Fluoride Elution Techniques for the Enhancement of Copper-Mediated Late-Stage Radiofluorination
AV Mossine, AF Brooks, N Ichiishi, KJ Makaravage, MS Sanford, ...
Scientific Reports 7 (1), 233, 2017
672017
Automated synthesis of PET radiotracers by copper‐mediated 18F‐fluorination of organoborons: Importance of the order of addition and competing protodeborylation
AV Mossine, AF Brooks, V Bernard‐Gauthier, JJ Bailey, N Ichiishi, ...
Journal of Labelled Compounds and Radiopharmaceuticals 61 (3), 228-236, 2018
522018
One-pot synthesis of high molar activity 6-[18 F] fluoro-l-DOPA by Cu-mediated fluorination of a BPin precursor
AV Mossine, SS Tanzey, AF Brooks, KJ Makaravage, N Ichiishi, JM Miller, ...
Organic & biomolecular chemistry 17 (38), 8701-8705, 2019
472019
Silver‐Catalyzed Allenylation and Enantioselective Propargylation Reactions of Ketones
BL Kohn, N Ichiishi, ER Jarvo
Angewandte Chemie 16 (125), 4510-4513, 2013
442013
New avenues in radical trifluoromethylselenylation with trifluoromethyl tolueneselenosulfonate
C Ghiazza, C Monnereau, L Khrouz, M Médebielle, T Billard, A Tlili
Synlett 30 (07), 777-782, 2019
362019
Synthesis of high-molar-activity [18F]6-fluoro-l-DOPA suitable for human use via Cu-mediated fluorination of a BPin precursor
AV Mossine, SS Tanzey, AF Brooks, KJ Makaravage, N Ichiishi, JM Miller, ...
Nature protocols 15 (5), 1742-1759, 2020
342020
C–H 18 F-fluorination of 8-methylquinolines with Ag [18 F] F
SJ Lee, AF Brooks, N Ichiishi, KJ Makaravage, AV Mossine, MS Sanford, ...
Chemical Communications 55 (20), 2976-2979, 2019
222019
Thioesterification and selenoesterification of amides via selective N–C cleavage at room temperature: N–C (O) to S/Se–C (O) interconversion
MM Rahman, G Li, M Szostak
Synthesis 52 (07), 1060-1066, 2020
212020
Emerging fluorination methods in organic chemistry relevant for life science application
KD Dykstra, N Ichiishi, SW Krska, PF Richardson
Fluorine in Life Sciences: Pharmaceuticals, Medicinal Diagnostics, and …, 2019
212019
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
Reducing Limitation in Probe Design: The Development of a Diazirine-Compatible Suzuki–Miyaura Cross Coupling Reaction
N Ichiishi, KP Moore, AM Wassermann, SE Wolkenberg, SW Krska
ACS Medicinal Chemistry Letters 10 (1), 56-61, 2018
162018
Catalytic sulfamoylation of alcohols with activated aryl sulfamates
PB Rapp, K Murai, N Ichiishi, DK Leahy, SJ Miller
Organic letters 22 (1), 168-174, 2019
122019
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