Bioactive molecules synthesis

Keywords Bioactive molecules synthesis Transition metals... 

Aziridines are versatile intermediates in organic synthesis and commonly found in bioactive molecules. The transition metal-catalyzed nitrene transfer to alkenes is an attractive method for the synthesis of aziridines [7]. In 1984, Mansuy and coworkers reported the first example of an iron-catalyzed alkene aziridination in which iron porphyrin [Fe(TTP)Cl] was used as catalyst and PhINTs was used as nitrene source [30]. Subsequently, the same authors demonstrated that [Fe(TDCPP) (CIO4)] is a more efficient and selective catalyst than [Fe(TTP)Cl] (Scheme 20). 

Matsumoto K (2007) High-Pressure Synthesis of Heterocycles Related to Bioactive Molecules. 8 1-42... 

The term biology-oriented synthesis (BIOS) [45] has been used to describe the design of compound libraries based on biologically relevant chemical space [46]. The areas in protein structures that participate in productive protein-ligand interactions have been, for the most part, already defined by natural products and drugs. Thus libraries inspired by natural products and other bioactive molecules are expected to have a higher probability of biologically activity than randomly synthesized molecules [47,48]. 

The enantioselective reduction of unsaturated alcohol derivatives has been applied to the synthesis of several biologically active compounds (Scheme 24.12). Warfarin (123, R=H) is an important anticoagulant that is normally prescribed as the racemate, despite the enantiomers having dissimilar pharmacological profiles. One of the earliest reported uses of DuPhos was in the development of a chiral switch for this bioactive molecule, facilitating the preparation of (R)- and (S)-warfarin [184]. Although attempted reduction of the parent hydroxycoumarin 122 (R=H) led to formation of an unreactive cyclic hemiketal, hydrogenation of the sodium salt proceeded smoothly with Rh-Et-DuPhos in 86-89% ee. 

This chapter has introduced the aldol and related allylation reactions of carbonyl compounds, the allylation of imine compounds, and Mannich-type reactions. Double asymmetric synthesis creates two chiral centers in one step and is regarded as one of the most efficient synthetic strategies in organic synthesis. The aldol and related reactions discussed in this chapter are very important reactions in organic synthesis because the reaction products constitute the backbone of many important antibiotics, anticancer drugs, and other bioactive molecules. Indeed, study of the aldol reaction is still actively pursued in order to improve reaction conditions, enhance stereoselectivity, and widen the scope of applicability of this type of reaction. 

Aminosulfides, important building blocks for the synthesis of various bioactive molecules, can be prepared by the thiolysis of aziridines in the presence of Bi(OTf)3 (5 mol%) [36]. Even though Lewis acids such as boron trifluoride etherate and zinc chloride, as well as Bronsted acids such as trifluoromethanesulfonic acid, have been employed as acid catalysts, these methods suffer from disadvantages like the use of stoichiometric amount of catalysts [37—40], harsh conditions, the use of large excess of thiols and necessitate anhydrous conditions to produce the desired products. Furthermore, these reagents cannot be recovered and recycled because they decompose or deactivate under quenching conditions. 

Pal A (2004) Photochemical synthesis of gold nanoparticles via controlled nucleation using a bioactive molecule. Mater Lett 58 529-534... 

VIII. Synthesis of Natural Products and Related Bioactive Molecules via... 

This section covers the synthesis of aziridines, oxiranes, /J-lactams and oxetanes. Aziridines are fairly important moieties in bioactive molecules and thus new routes for their synthesis are constantly being developed. /1-Lactams are probably the most important heterocyclic compounds that contain a single nitrogen atom, due to their importance in penicillin and cephalosporin chemistry. Their synthesis and chemistry has received much attention and much of this work has been reviewed544. The oxygen-containing heterocycles are much less commonly synthesized from double-bonded functional groups. 

High-Pressure Synthesis of Heterocycles Related to Bioactive Molecules... 

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