The recent advances in nanotechnology and the corresponding increase in the use of nanomaterials in products in every sector of society have resulted in uncertainties regarding environmental impacts. The objectives of this review are to introduce the key aspects pertaining to nanomaterials in the environment and to discuss what is known concerning their fate, behavior, disposition, and toxicity, with a particular focus on those that make up manufactured nanomaterials. This review critiques existing nanomaterial research in freshwater, marine, and soil environments. It illustrates the paucity of existing research and demonstrates the need for additional research. Environmental scientists are encouraged to base this research on existing studies on colloidal behavior and toxicology. The need for standard reference and testing materials as well as methodology for suspension preparation and testing is also discussed.

Nanomaterials in the environment: Behavior, fate, bioavailability, and effects

Since the discovery of organic azides by Peter Griess more than 140 years ago, numerous syntheses of these energy-rich molecules have been developed. In more recent times in particular, completely new perspectives have been developed for their use in peptide chemistry, combinatorial chemistry, and heterocyclic synthesis. Organic azides have assumed an important position at the interface between chemistry, biology, medicine, and materials science. In this Review, the fundamental characteristics of azide chemistry and current developments are presented. The focus will be placed on cycloadditions (Huisgen reaction), aza ylide chemistry, and the synthesis of heterocycles. Further reactions such as the aza-Wittig reaction, the Sundberg rearrangement, the Staudinger ligation, the Boyer and Boyer-Aube rearrangements, the Curtius rearrangement, the Schmidt rearrangement, and the Hemetsberger rearrangement bear witness to the versatility of modern azide chemistry.

Organic Azides: An Exploding Diversity of a Unique Class of Compounds

Asymmetric 1,3-Dipolar Cycloaddition Reactions

One of the initial steps in the development of therapeutic agents is the identification of lead compounds that bind to the receptor or enzyme target of interest. Many analogs of these lead compounds are then synthesized to define the key recognition elements for maximal activity. In general, many compounds must be evaluated in both the lead identification and optimization steps. Increasing burdens have been placed on these efforts due to the large number of new therapeutic targets that continue to be identified thorough modern molecular biology methods.1 To address this demand, very powerful chemical and biological methods have been developed for the generation of large combinatorial libraries of peptides2 and oligonucleotides3 that are then screened against a receptor or enzyme to identify high-affinity ligands or potent inhibitors, respectively. While these studies have clearly demonstrated the power of library synthesis and screening strategies, peptides and oligonucleotides generally have poor oral activities and rapid in vivo clearance;4 therefore their utility as bioavailable therapeutic agents is often limited. Due to the favorable pharmacokinetic properties of many small organic molecules (<600-700 molecular weight),5 the design, synthesis, and evaluation of libraries of these compounds6 has rapidly become a major frontier in organic chemistry. Lorin A. Thompson was born in Lexington, KY, in 1970. He received the Bachelor of Science degree from the University of North Carolina, Chapel Hill, in 1992 where he worked under the guidance of Joseph Desimone. He is currently pursuing his doctorate in the laboratory of Jonathan Ellman at UC Berkeley where he is the 1994 Glaxo-Wellcome fellow. His research interests include the development of synthetic methodology for organic library construction.

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Synthesis and Applications of Small Molecule Libraries.

1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

By the action of butyllithium or lithium metal in such polar aprotic solvent as DMF or HMPA in the presence of aldehydes or related compounds, some benzylsilanes suffer from anion radical-induced desilylation forming benzyl carbanions which add to the aldehydes and related compounds

Anion radical-induced desilylation of organosilane. Reactions of benzylsilanes with aldehydes and related compounds in the presence of butyllithium or lithium metal

Cycloaddition of New N-Unsubstituted Azomethine Ylides Generated from N-[(Trimethylsilyl)methyl]thiocarbamates, Synthetic Equivalents of Non-stabilized Alkoxy- or Alkylthionitrile Ylides.

A synthetic equivalent of parent azomethine imine is accessible by simple heating of ethyl 3-benzylcarbazate with paraformaldehyde under reflux in toluene in the presence of triethylamine, which effectively suppresses the undesired formation of imine dimers. The resulting imines can be trapped with a variety of dipolarophiles.

Triethylamine‐Mediated Generation of a Synthetic Equivalent of Parent Azomethine Imine by Condensation of Ethyl 3‐Benzylcarbazate with Paraformaldehyde.

A sequence of cycloadditions of (diethoxyphosphinyl)acetonitrile oxide with α,β-unsaturated esters, the Raney Ni reduction of the resulting cycloadducts, the Horner–Emmons olefination, and the carbonyl reduction with sodium borohydride leads to 5-[(E)-1-alkenyl]-3-hydroxy-4,5-dihydro-2(3H)-furanones which can be converted into (Z)-5-alkylidene-2(5H)-furanones in two steps.

Synthesis of 4‐((E)‐1‐Alkenyl)‐2‐hydroxybutanolides and (Z)‐4‐Alkylidene‐2‐butenolides Through Cycloadditions Using a Phosphorus‐Functionalized Nitrile Oxide

Otohiko Tsuge

Papers

Anion radical-induced desilylation of organosilane. Reactions of benzylsilanes with aldehydes and related compounds in the presence of butyllithium or lithium metal

Cycloaddition of New N-Unsubstituted Azomethine Ylides Generated from N-[(Trimethylsilyl)methyl]thiocarbamates, Synthetic Equivalents of Non-stabilized Alkoxy- or Alkylthionitrile Ylides.

Triethylamine‐Mediated Generation of a Synthetic Equivalent of Parent Azomethine Imine by Condensation of Ethyl 3‐Benzylcarbazate with Paraformaldehyde.

Synthesis of 4‐((E)‐1‐Alkenyl)‐2‐hydroxybutanolides and (Z)‐4‐Alkylidene‐2‐butenolides Through Cycloadditions Using a Phosphorus‐Functionalized Nitrile Oxide

Studies of acenaphthene derivatives. XVIII. The novel reaction of benzylideneacenaphtenones with grignard reagents