相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Iron/Copper Co-Catalyzed Cross-Coupling Reaction for the Synthesis of 6-Substituted 7-Deazapurines and the Corresponding Nucleosides
Qingfeng Li et al.
JOURNAL OF ORGANIC CHEMISTRY (2020)
General C(sp2)-C(sp3) Cross-Electrophile Coupling Reactions Enabled by Overcharge Protection of Homogeneous Electrocatalysts
Blaise L. Truesdell et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2020)
Chemistry and Biology of SARS-CoV-2
Alexander Domling et al.
CHEM (2020)
Metal-Reductant-Free Electrochemical Nickel-Catalyzed Couplings of Aryl and Alkyl Bromides in Acetonitrile
Robert J. Perkins et al.
ORGANIC PROCESS RESEARCH & DEVELOPMENT (2019)
Metal-free defluorinative arylation of trifluoromethyl alkenes via photoredox catalysis
Rebecca J. Wiles et al.
CHEMICAL COMMUNICATIONS (2019)
Organocatalyzed, Visible-Light Photoredox-Mediated, One-Pot Minisci Reaction Using Carboxylic Acids via N-(Acyloxy)phthalimides
Trevor C. Sherwood et al.
JOURNAL OF ORGANIC CHEMISTRY (2018)
A radical approach to the copper oxidative addition problem: Trifluoromethylation of bromoarenes
Chip Le et al.
SCIENCE (2018)
Photoredox-Assisted Reductive Cross-Coupling: Mechanistic Insight into Catalytic Aryl-Alkyl Cross-Couplings
Avishek Paul et al.
JOURNAL OF ORGANIC CHEMISTRY (2017)
Electrochemical Nickel Catalysis for Sp2-Sp3 Cross-Electrophile Coupling Reactions of Unactivated Alkyl Halides
Robert J. Perkins et al.
ORGANIC LETTERS (2017)
Modular, Step-Efficient Palladium-Catalyzed Cross-Coupling Strategy To Access C6-Heteroaryl 2-Aminopurine Ribonucleosides
Helena S. Buchanan et al.
ORGANIC LETTERS (2017)
A General Small-Scale Reactor To Enable Standardization and Acceleration of Photocatalytic Reactions
Chi Chip Le et al.
ACS CENTRAL SCIENCE (2017)
An Improved System for the Aqueous Lipshutz-Negishi Cross-Coupling of Alkyl Halides with Aryl Electrophiles
Vasudev R. Bhonde et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)
Exploring the purine core of 3′-C-ethynyladenosine (EAdo) in search of novel nucleoside therapeutics
Fabian Hulpia et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2016)
Silyl Radical Activation of Alkyl Halides in Metallaphotoredox Catalysis: A Unique Pathway for Cross-Electrophile Coupling
Patricia Zhang et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2016)
Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Alkyl Bromides: Et3N as the Terminal Reductant
Zhengli Duan et al.
ORGANIC LETTERS (2016)
1,4-Dihydropyridines as Alkyl Radical Precursors: Introducing the Aldehyde Feedstock to Nickel/Photoredox Dual Catalysis
Alvaro Gutierrez-Bonet et al.
ACS CATALYSIS (2016)
Applications of Fluorine in Medicinal Chemistry
Eric P. Gillis et al.
JOURNAL OF MEDICINAL CHEMISTRY (2015)
6-(Hetero)Arylpurine nucleotides as inhibitors of the oncogenic target DNPH1: Synthesis, structural studies and cytotoxic activities
Claire Amiable et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2014)
Reductive Cross-Coupling of Nonaromatic, Heterocyclic Bromides with Aryl and Heteroaryl Bromides
Gary A. Molander et al.
JOURNAL OF ORGANIC CHEMISTRY (2014)
Radical Route for the Alkylation of Purine Nucleosides at C6 via Minisci Reaction
Ran Xia et al.
ORGANIC LETTERS (2014)
Amine α-heteroarylation via photoredox catalysis: a homolytic aromatic substitution pathway
Christopher K. Prier et al.
CHEMICAL SCIENCE (2014)
Advances in the development of nucleoside and nucleotide analogues for cancer and viral diseases
Lars Petter Jordheim et al.
NATURE REVIEWS DRUG DISCOVERY (2013)
Cladribine as a therapeutic option in multiple sclerosis
Clemens Warnke et al.
CLINICAL IMMUNOLOGY (2012)
Synthesis and evaluation of the substrate activity of C-6 substituted purine ribosides with E. coli purine nucleoside phosphorylase: Palladium mediated cross-coupling of organozinc halides with 6-chloropurine nucleosides [1]
Abdalla E. A. Hassan et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2012)
Replacing Conventional Carbon Nucleophiles with Electrophiles: Nickel-Catalyzed Reductive Alkylation of Aryl Bromides and Chlorides
Daniel A. Everson et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2012)
Nickel-Catalyzed Reductive Coupling of Aryl Halides with Secondary Alkyl Bromides and Allylic Acetate
Shulin Wang et al.
ORGANIC LETTERS (2012)
Dual pro-drugs of 2′-C-methyl guanosine monophosphate as potent and selective inhibitors of hepatitis C virus
Christopher McGuigan et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2011)
The many faces of the adamantyl group in drug design
Joe Liu et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2011)
Synthesis and biological activity of novel N6-substituted and 2,N6-disubstituted adenine ribo- and 3′-C-methyl-ribonucleosides as antitumor agents
Loredana Cappellacci et al.
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY (2011)
Microwave promoted C6-alkylation of purines through SNAr-based reaction of 6-chloropurines with 3-alkyl-acetylacetone
Hai-Ming Guo et al.
ORGANIC & BIOMOLECULAR CHEMISTRY (2011)
Direct Method for Carbon-Carbon Bond Formation: The Functional Group Tolerant Cobalt-Catalyzed Alkylation of Aryl Halides
Muriel Amatore et al.
CHEMISTRY-A EUROPEAN JOURNAL (2010)
Escape from Flatland: Increasing Saturation as an Approach to Improving Clinical Success
Frank Lovering et al.
JOURNAL OF MEDICINAL CHEMISTRY (2009)
An Efficient and Diastereoselective Synthesis of PSI-6130: A Clinically Efficacious Inhibitor of HCV NS5B Polymerase
Peiyuan Wang et al.
JOURNAL OF ORGANIC CHEMISTRY (2009)
Zn-Mediated, Pd-Catalyzed Cross-Couplings in Water at Room Temperature Without Prior Formation of Organozinc Reagents
Arkady Krasovskiy et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2009)
Straightforward and Highly Efficient Catalyst-Free One-Step Synthesis of 2-(Purin-6-yl)acetoacetic Acid Ethyl Esters, (Purin-6-yl)acetates, and 6-Methylpurines through SNAr-Based Reactions of 6-Halopurines with Ethyl Acetoacetate
Gui-Rong Qu et al.
ORGANIC LETTERS (2009)
Direct Cobalt-Catalyzed Cross-Coupling Between Aryl and Alkyl Halides
Waldemar Maximilian Czaplik et al.
SYNLETT (2009)
Synthesis, biological evaluation and molecular modeling studies of N6-benzyladenosine analogues as potential anti-toxoplasma agents
Young Ah Kim et al.
BIOCHEMICAL PHARMACOLOGY (2007)
Design, synthesis, and antiviral activity of 2′-deoxy-2′-fluoro-2′-C-methylcytidine, a potent inhibitor of hepatitis C virus replication
JL Clark et al.
JOURNAL OF MEDICINAL CHEMISTRY (2005)
Synthesis and biological evaluation of 6-substituted purine and 9-β-D-ribofuranosyl purine analogues
JF Wang et al.
BIOORGANIC & MEDICINAL CHEMISTRY (2004)