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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Sulfanylbenzamide is an herbicide that inhibits the growth of plants by inhibiting the production of chlorophyll. It is a halogen that binds to cycloalkyl, which prevents the formation of phenylalanine, leading to cell death. 3-Sulfanylbenzamide has been shown to be effective in controlling the growth of weeds such as lambsquarters and ragweed.</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>1,2λ⁶,3-Oxathiazinane-2,2-dione is a cyclization reaction product of 1,2λ⁶,3-oxathiazine and 2-mercaptobenzothiazole. It is an intramolecular reaction that produces a six-membered ring containing two heteroatoms. This product can be used as a reagent for the oxidation of sulfamates to sulfoxides. The radical reaction mechanism of this compound has been studied with the use of intermediacy and mechanistic studies. Hypervalent cations catalyze this process and it occurs in the presence of organic esters.</p>

<p>Versatile small molecule scaffold</p>

<p>(S)-tert-Butyl 3-bromopyrrolidine-1-carboxylate is a reagent that can be used for the synthesis of chiral compounds. It reacts with chlorosulfonyl isocyanate to form an N-substituted sulfonamide. This reaction proceeds with high stereoselectivity, yielding the desired product in high yield and enantiomeric excess. (S)-tert-Butyl 3-bromopyrrolidine-1-carboxylate can also be used as a desulfonylation reagent and has been shown to react with c1–c6 alkoxy groups to form alcohols. (S)-tert-Butyl 3-bromopyrrolidine-1-carboxylate reacts with nitro groups to form nitroso derivatives, octane to produce cyclohexanones, benzyl group to make phenols, piperidine to</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>3-(Boc-amino)pyridine-2-carboxylic acid is a chiral, stereoselective compound that can be synthesized by reacting an achiral amine with a carbamic acid. The yields of the reaction are high and the product is obtained in a single step. 3-(Boc-amino)pyridine-2-carboxylic acid can be used as an intermediate for the synthesis of β-lactams, which are important for their antibiotic properties. The diastereomer is formed when the amino group on the molecule interacts with either right or left side of the carbonyl group. This interaction leads to different configurations and stereoisomers.</p>

Versatile small molecule scaffold