Catalytic dehydrogenative cross-coupling: forming carbon-carbon bonds by oxidizing two carbon-hydrogen bonds

Protic Ionic Liquids: Properties and Applications

4.2.8. Reductive Coupling 3109 5. Reaction of Aromatic Compounds 3110 5.1. Electrophilic Substitutions 3110 5.2. Radical Substitution 3111 5.3. Oxidative Coupling 3111 5.4. Photochemical Reactions 3111 6. Reaction of Carbonyl Compounds 3111 6.1. Nucleophilic Additions 3111 6.1.1. Allylation 3111 6.1.2. Propargylation 3120 6.1.3. Benzylation 3121 6.1.4. Arylation/Vinylation 3121 6.1.5. Alkynylation 3121 6.1.6. Alkylation 3121 6.1.7. Reformatsky-Type Reaction 3122 6.1.8. Direct Aldol Reaction 3122 6.1.9. Mukaiyama Aldol Reaction 3124 6.1.10. Hydrogen Cyanide Addition 3125 6.2. Pinacol Coupling 3126 6.3. Wittig Reactions 3126 7. Reaction of R,â-Unsaturated Carbonyl Compounds 3127

Organic Reactions in Aqueous Media with a Focus on Carbon−Carbon Bond Formations: A Decade Update

III. Foldamer Research 3910 A. Overview 3910 B. Motivation 3910 C. Methods 3910 D. General Scope 3912 IV. Peptidomimetic Foldamers 3912 A. The R-Peptide Family 3913 1. Peptoids 3913 2. N,N-Linked Oligoureas 3914 3. Oligopyrrolinones 3915 4. Oxazolidin-2-ones 3916 5. Azatides and Azapeptides 3916 B. The â-Peptide Family 3917 1. â-Peptide Foldamers 3917 2. R-Aminoxy Acids 3937 3. Sulfur-Containing â-Peptide Analogues 3937 4. Hydrazino Peptides 3938 C. The γ-Peptide Family 3938 1. γ-Peptide Foldamers 3938 2. Other Members of the γ-Peptide Family 3941 D. The δ-Peptide Family 3941 1. Alkene-Based δ-Amino Acids 3941 2. Carbopeptoids 3941 V. Single-Stranded Abiotic Foldamers 3944 A. Overview 3944 B. Backbones Utilizing Bipyridine Segments 3944 1. Pyridine−Pyrimidines 3944 2. Pyridine−Pyrimidines with Hydrazal Linkers 3945

A field guide to foldamers.

Structure and nanostructure in ionic liquids.

The room-temperature liquid salt, ethylammonium nitrate (EAN), has been used to enhance the recovery of denatured-reduced hen egg white lysozyme (HEWL). Our results show that EAN has the ability to prevent aggregation of the denatured protein. The use of EAN as a refolding additive is advantageous because the renaturation is a one-step process. When HEWL was denatured reduced using routine procedures and renatured using EAN as an additive, HEWL was found to regain 75% of its activity. When HEWL was denatured and reduced in neat EAN, dilution resulted in over 90% recovery of active protein. An important aspect of this process is that renaturation of HEWL occurs at concentrations of 1.6 mg/mL, whereas other renaturation processes occur at significantly lower protein concentrations. Additionally, the refolded-active protein can be separated from the molten salt by simple desalting methods. Although the use of a low-temperature molten salt in protein renaturation is unconventional, the power of this approach lies in its simplicity and utility.

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Protein renaturation by the liquid organic salt ethylammonium nitrate

This paper describes the design, synthesis, and characterization of a hydrogen-bonded molecular duplex (3·4). Two oligoamide molecular strands, 3 and 4, with the complementary hydrogen-bonding sequences ADAADA and DADDAD, respectively, were found to form an extremely stable (Ka = (1.3 ± 0.7) × 109 M-1) molecular duplex (3·4) in chloroform. Evidence from 1D and 2D 1H NMR spectroscopy, isothermal titration calorimetry, and thin-layer chromatography confirmed the formation and the high stability of the duplex. The exceptional stability is explained by positive cooperativity among the numerous hydrogen-bonding and van der Waals interactions and the preorganization of the individual strands by intramolecular hydrogen bonds. This design has opened a new avenue to supramolecular recognition units with programmable specificities and stabilities.

A Highly Stable, Six-Hydrogen-Bonded Molecular Duplex

Electrochemical investigation of the reducing power of SmI2 in THF and the effect of HMPA cosolvent

This account describes work, performed by my research group during the past decade, designed to understand the mechanistic roles of cosolvents and additives in reductions involving samarium(II) iodide (SmI 2 ). Emphasis is placed on studies designed to elucidate the roles of the cosolvent hexamethylphosphoramide (HMPA) and proton donors (water, alcohols, and glycols) in the mechanisms of important bond-forming reactions and reductions initiated by SmI 2 . 1 Background and Introduction 1.1 Project Inception 2 Mechanistic Studies on the Role of Hexamethylphosphor-amide in the Reactions of Samarium(II) Iodide 3 Impact of Proton Donors on the Mechanism of Substrate Reduction 4 Conclusions and Future Work

Mechanistic Studies on the Roles of Cosolvents and Additives in Samarium(II)-Based Reductions

Native coals are strained and glassy. When coals are swollen, this strain is relieved as the coal structure rearranges to a lower free energy and more highly noncovalently associated state. Four coals ranging in carbon content from 77% C to 84% C were warmed in the weak swelling solvent chlorobenzene at 132 °C for 2 weeks and samples were withdrawn at intervals. After evaporation of the chlorobenzene, the pyridine extractability of the treated coals had decreased, sometimes by a factor of 2. The pyridine swelling of Pittsburgh No. 8 coal was sharply reduced. The extractability and swelling decreases with time demonstrate that changes in coal structure occurred with the rearranged coal being more associated. This increased association is not due to hydrogen bond formation because pyridine is known to break most if not all of the hydrogen bonds which occur in coals. The rearranged Pittsburgh No. 8 coal was studied by differential scanning calorimetry. Over the 2 week chlorobenzene reflux period, the heat ca...

Robert A. Flowers

Papers

Protein renaturation by the liquid organic salt ethylammonium nitrate

A Highly Stable, Six-Hydrogen-Bonded Molecular Duplex

Electrochemical investigation of the reducing power of SmI2 in THF and the effect of HMPA cosolvent

Mechanistic Studies on the Roles of Cosolvents and Additives in Samarium(II)-Based Reductions

Structural Rearrangement of Strained Coals