Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(1S)-1-(4-Iodophenyl)ethan-1-ol is an electrophilic reagent that is used in the synthesis of imidazoles. It is generated by the chemoenzymatic, regioselective alkylation of a phenyl ring with a stannylated phenyl amine. This process can be performed using a variety of different reagents and solvents, including N-chloro-N-methylpyridinium tetrafluoroborate (NCMP). The regioselectivity of the reaction ensures that the desired product is generated in high yield.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,6-Dibromo-3-methoxypyridine is an important intermediate for the synthesis of polymers and copolymers. It can be obtained by cross-coupling reactions with a variety of electrophiles such as alkyl halides and organometallic compounds. This compound can also be prepared by electrochemical synthesis in the presence of a suitable catalyst such as copper oxide or nickel oxide. The insoluble nature of 2,6-dibromo-3-methoxypyridine makes it difficult to isolate.<br>2,6-Dibromo-3-methoxypyridine is used in the preparation of thiophene, stannylated pyridines, and ethers. It has also been used in the synthesis of polymers and copolymers with a variety of monomers including styrene, vinyl acetate, acrylonitrile, methyl methacrylate, methyl ac</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Iodoquinoline is a quinoline derivative that has antifungal activity against opportunistic fungal organisms, such as Cryptococcus neoformans. This drug is synthesized by the reaction of terminal alkynes with azides in the presence of copper (II) chloride. 3-Iodoquinoline is an efficient method for the synthesis of cross-coupling reactions and can be scaled up to produce milligram quantities. 3-Iodoquinoline has been shown to be effective against Candida glabrata and Cryptococcus neoformans at concentrations of 1 μg/mL or less. This drug also inhibits cell growth in vitro and in vivo, which may be due to its ability to inhibit protein synthesis and DNA synthesis.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Fluoro-4,5-dimethoxybenzoic acid is a fluorinated electrophilic side-chain oxazoline. It is synthesized by lithiation of 2,4,5-trimethoxybenzaldehyde followed by oxidation with hydrogen peroxide and reductive cleavage with sodium borohydride. The fluorination of the 2-position of the benzoic acid moiety provides a convenient method for preparing fluorinated analogues that are resistant to degradation.</p>

<p>Versatile small molecule scaffold</p>

<p>4,5-Dihydrothieno[2,3-c]pyrrol-6-one is an organic compound that is used as a starting material for the synthesis of other compounds. It can be prepared by refluxing carbon tetrachloride and potassium carbonate in methanol solution with bromosuccinimide as an initiator. The yield of 4,5-dihydrothieno[2,3-c]pyrrol-6-one is about 60%.</p>

<p>4-Phenyl-2-(piperazin-1-yl)quinazoline is a ligand that has been shown to bind to integrin alphaIIbbeta3. It has also been shown to inhibit the activity of human platelets and potently inhibit the activity of human thrombin. The molecular docking studies have shown that this ligand interacts with the binding site on the integrin alphaIIbbeta3, which is responsible for the binding of a number of ligands. This compound has been found to be an affinity and potent inhibitor of platelet activation, which may be due to its inhibition of integrin alphaIIbbeta3.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>