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A Cobalt Templated Chiral Outer Sphere Hydrogen Bond Donor Catalyst Derived from 2-Guanidinobenzimidazole: Synthesis, Applications in Carbon-Carbon Bond Forming Reactions, Structure
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Versatile behavior of 2-guanidinobenzimidazole nitrogen atoms toward protonation, coordination and methylation
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Metal‐Free Synthesis of Cyclic and Acyclic Carbonates from CO2 and Alcohols
inferredcites →https://doi.org/10.1002/ejoc.202200950openalex-extracted
Recent Developments and Trends in Asymmetric Organocatalysis
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Enantioselective Organocatalytic Michael Addition Reactions Catalyzed by Proline/Prolinol/Supported Proline based Organocatalysts: An Overview
inferredcites →https://doi.org/10.1007/bf00166009openalex-extracted
Coordination behaviour of 2-guanidinobenzimidazole towards cobalt(II), nickel(II), copper(II) and zinc(II). An experimental and theoretical study
inferredcites →https://doi.org/10.1016/s0010-8545(99)00153-8openalex-extracted
Coordination chemistry of some biologically active ligands
inferredcites →https://doi.org/10.1021/acs.accounts.0c00410openalex-extracted
Launching Werner Complexes into the Modern Era of Catalytic Enantioselective Organic Synthesis
inferredcites →https://doi.org/10.1021/acs.inorgchem.1c00855openalex-extracted
Synthesis and a Catalytic Study of Diastereomeric Cationic Chiral-at-Cobalt Complexes Based on (R,R)-1,2-Diphenylethylenediamine
inferredcites →https://doi.org/10.1021/acs.joc.8b01695openalex-extracted
Diphenyl Carbonate: A Highly Reactive and Green Carbonyl Source for the Synthesis of Cyclic Carbonates
inferredcites →https://doi.org/10.1021/acs.organomet.0c00073openalex-extracted
Chiral-at-Metal Ruthenium Complexes with Guanidinobenzimidazole and Pentaphenylcyclopentadienyl Ligands: Synthesis, Resolution, and Preliminary Screening as Enantioselective Second Coordination Sphere Hydrogen Bond Donor Catalysts
inferredcites →https://doi.org/10.1021/acs.organomet.2c00590openalex-extracted
Post-Modification of Octahedral Chiral-at-Metal Cobalt(III) Complexes by Suzuki–Miyaura Cross-Coupling and Evaluation of Their Catalytic Activity
inferredcites →https://doi.org/10.1021/acscatal.1c01883openalex-extracted
Chiral Cobalt(III) Tris(1,2-diamine) Catalysts That Incorporate Nitrogenous Base Containing Anions for the Bifunctional Activation of Nucleophiles and Electrophiles in Enantioselective Addition Reactions
inferredcites →https://doi.org/10.1021/acscatal.9b05496openalex-extracted
Chiral Tricationic Tris(1,2-diphenylethylenediamine) Cobalt(III) Hydrogen Bond Donor Catalysts with Defined Carbon/Metal Configurations; Matched/Mismatched Effects upon Enantioselectivities with Enantiomeric Chiral Counter Anions
inferredcites →https://doi.org/10.1021/acsomega.0c06265openalex-extracted
Utilization of Guanidine-Based Ancillary Ligands in Arene–Ruthenium Complexes for Selective Cytotoxicity
inferredcites →https://doi.org/10.1021/cs500134zopenalex-extracted
Highly Active Families of Catalysts for the Ring-Opening Polymerization of Lactide: Metal Templated Organic Hydrogen Bond Donors Derived from 2-Guanidinobenzimidazole
inferredcites →https://doi.org/10.1021/om0103097openalex-extracted
Kinetics and Mechanisms of Methyl Vinyl Ketone Hydroalkoxylation Catalyzed by Palladium(II) Complexes
inferredcites →https://doi.org/10.1021/om500704uopenalex-extracted
Metal-Templated Hydrogen Bond Donors as “Organocatalysts” for Carbon–Carbon Bond Forming Reactions: Syntheses, Structures, and Reactivities of 2-Guanidinobenzimidazole Cyclopentadienyl Ruthenium Complexes
inferredcites →https://doi.org/10.1039/c2cs15234gopenalex-extracted
Chiral-at-metal complexes and their catalytic applications in organic synthesis
inferredcites →https://doi.org/10.1039/d0dt00523aopenalex-extracted
Rendering classical hydrophilic enantiopure Werner salts [M(en) 3 ] n+ n X − lipophilic (M/ n = Cr/3, Co/3, Rh/3, Ir/3, Pt/4); new chiral hydrogen bond donor catalysts and enantioselectivities as a function of metal and charge
inferredcites →https://doi.org/10.1039/p298700000s1openalex-extracted
Tables of bond lengths determined by X-ray and neutron diffraction. Part 1. Bond lengths in organic compounds
inferredcites →https://doi.org/10.1055/s-0042-1751492openalex-extracted
Recent Advancements in Typical Friedel–Crafts Alkylation Reactions Focused on Targeting Arene Nucleophiles
inferredcites →https://doi.org/10.1107/s0021889802022112openalex-extracted
Single-crystal structure validation with the program PLATON
inferredcites →https://doi.org/10.1107/s0021889808042726openalex-extracted
OLEX2 : a complete structure solution, refinement and analysis program
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