Synthetic approaches chemistry

Galm, U., Dessoy, M. A., Schmidt, J., Wessjohann, L. A., 8c Heide, L. (2004). In vitro and in vivo production of new aminocoumarins by a combined biochemical, genetic and synthetic approach. Chemistry Biology, 11,173. 

Cytokines, eg, interferons, interleukins, tumor necrosis factor (TNF), and certain growth factors, could have antitumor activity directiy, or may modulate cellular mechanisms of antitumor activity (2). Cytokines may be used to influence the proliferation and differentiation of T-ceUs, B-ceUs, macrophage—monocyte, myeloid, or other hematopoietic cells. Alternatively, the induction of interferon release may represent an important approach for synthetic—medicinal chemistry, to search for effective antiinflammatory and antifibrotic agents. Inducers of interferon release may also be useful for lepromatous leprosy and chronic granulomatous disease. The potential cytokine and cytokine-related therapeutic approaches to treatment of disease are summarized in Table 4. A combination of cytokines is a feasible modaUty for treatment of immunologically related diseases however, there are dangers inherent in such an approach, as shown by the induction of lethal disserninated intravascular coagulation in mice adrninistered TNF-a and IFN-y. 

The first synthetic route for isocyanates was reported in 1848 (10,11)- Subsequent efforts by Hofmann, Curtius, and Hentschel pioneered alternative synthetic approaches (12). These efforts highlighted the phosgene—amine approach. Staudinger presented the stmctural similarities between isocyanates and ketenes and stimulated interest in this class of compounds (13). However, it was not until 1945, when the world was pressed for an alternative to natural mbber, that synthetic routes to isocyanates became an area of great importance. Several excellent review articles covering the synthesis and chemistry of isocyanates have been presented (1 9). 

Other approaches to direct C2Q couplings have been reported (9,30—35). Based on their knowledge of sulfone chemistry, Rhc ne-Poulenc has patented many syntheses of P-carotene which use this olefination chemistry (36—41). Homer-Emmons chemistry has also been employed for this purpose (42). The synthetic approaches to the carotenoids have been reviewed (43). 

Several reviews deal with the chemistry of these unsaturated lactones (64CRV-353 68RCR254 76CRV625 77UK1250 82CSR75). Synthetic approaches to these compounds have recently been reviewed (94COS287 95COS133). 

Poly(p-pheny lene)s, PPPs, constitute the prototype of rigid-rod polymers and are currently being intensively investigated [1]. The key role of PPPs follows from their conceptually simple and appealing molecular structure, from their chemical stability, and from their superior physical properties [2], In turn, this is the result of important advances made in aromatic chemistry over the last few years. The following section gives an overview of the most common methods to generate poly(p-phenylene)s via different synthetic approaches. 

The known, in many cases very special, synthetic approaches to azocines often proceed via valence isomerization of appropriate precursor molecules. In this section these routes are classified by the last step in the reaction cascade. The synthesis and chemistry of azocines has been described in several excellent reviews,9-11 so that the treatment here is systematic and rather concise. 

Combinatorial chemistry constitutes a branch of the molecular sciences, providing an array of concepts and methods to solve molecular optimization problems (in drug research and beyond) more rapidly and efficiently than classical synthetic approaches. 

The best known of metal carbene reactions, cydopropanation reactions, have been used since the earliest days of diazo chemistry for addition reactions to the carbon-carbon double bond. Electron-donating groups (EDG) on the carbon-carbon double bond facilitate this catalytic reaction [37], whereas electron-withdrawing groups (EWG) inhibit addition while facilitating noncatalytic dipolar cycloaddition of the diazo compound [39] (Scheme 5). There are several reviews that describe the earlier synthetic approaches [1, 2,4, 5,40-43], and these will not be duplicated here. Focus will be given in this review to control of stereoselectivity. 

Soluble support-based synthetic approaches offer the advantages of both homogeneous solution-phase chemistry (high reactivity, ease of analysis) and solid-phase synthesis (large excess of reagents, simple product isolation and purification) [98,99]. As a representative example, PEG, one of the most widely used soluble polymers, has good solubility in most organic solvents (i.e., dichloromethane, acetonitrile, dimethylformamide, and toluene), but it... 

During the past 20 years, considerable progress has been made toward understanding the electronic properties of iron-sulfur centers thanks to the fruitful interplay between various approaches such as synthetic analog chemistry, theoretical modeling, and of course spectroscopic studies. Modeling studies have been strongly stimulated by the permanent supply of complementary data provided especially by EPR, Mossbauer, ENDOR, MCD, and NMR experiments. However,... 

Metal chalcogenides, apart from their technological significance in industrial applications, have played an important role in the development of new synthetic concepts and methods in the area of solid-state chemistry. A great example is alkali metal intercalation into TiS2 (Chap. 6) first reported three decades ago, which highlighted the then-novel synthetic approach called soft chemistry chimie douce). This low-temperature process allows for new compounds to be obtained while retaining the structural framework of the precursor. Related to this concept is the... 

These processes have flourished, mainly due to their selectivity and versatility, to the point where cross-coupling chemistry is often the initial thinking of organic chemists in synthetic and retro-synthetic approaches [2]. In fact, nowadays it is difficult to find a contribution in fine chemical or natural product synthesis where these molecular assembly tools are not employed. This is often due to the simple preparation and handling of the reaction partners as well as their relative compatibility with several functional groups. 

R. K. Bansal, Synthetic Approaches to Organic Chemistry, Jones and Bartlett, Sudbury, MA, 1998. 

Phosphorus is the most common donor atom in Ni° chemistry. Likewise, As- and Sb-based ligands are well suited for stabilizing low-valent Ni°. Ni° phosphine chemistry is extensive, and the general synthetic approaches have been summarized previously. 

Development of new synthetic routes to optically active (3-lactam derivatives is still an attractive problem in organic chemistry. As a synthetic approach to penicillin derivatives, photocyclization of oe-oxoamides 76 to (3-lactams has long been studied 41, 42). This reaction (Scheme 6), however, results in a complex mixture of racemic cis-and trans-isomers of (3-lactams 72 and of oxazolidin-4-ones 73, since the reaction proceeds via a zwitterionic intermediate 7143>. Of these isomers, only the optically... 

In our opinion, this approach provides not only a clear overview of the existing domino reactions, but also helps to develop new domino reactions and to initiate ingenious independent research projects in this important field of synthetic organic chemistry. 

Transition metal carbyne complexes are still relatively uncommon as only a few synthetic approaches to these compounds has proved generally applicable. In addition to making the initial characterization (723), the Fischer group has made the largest contribution to carbyne complex chemistry, with some 200 mononuclear complexes of Group 6 and 7 metals having been prepared. 

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