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  2. Diethylphosphite - Wikipedia

    en.wikipedia.org/wiki/Diethylphosphite

    Diethyl phosphite is the organophosphorus compound with the formula (C 2 H 5 O) 2 P(O)H. It is a popular reagent for generating other organophosphorus compounds, exploiting the high reactivity of the P-H bond.

  3. Phosphonate - Wikipedia

    en.wikipedia.org/wiki/Phosphonate

    In biochemistry and medicinal chemistry, phosphonate groups are used as stable bioisosteres for phosphate, such as in the antiviral nucleotide analog, Tenofovir, one of the cornerstones of anti-HIV therapy. And there is an indication that phosphonate derivatives are "promising ligands for nuclear medicine." [2]

  4. Aluminium diethyl phosphinate - Wikipedia

    en.wikipedia.org/wiki/Aluminium_diethyl_phosphinate

    Aluminium diethyl phosphinate is used as a halogen-free flame retardant for polyamides, polyesters, thermoset resins (e.g. epoxies) in electrical engineering and electronics (E&E) applications for switches, plugs, PC fans, and structural and housing components. Mobile phones, washing machines, and airplane parts, among others, contain the product.

  5. Acetylated distarch phosphate - Wikipedia

    en.wikipedia.org/wiki/Acetylated_distarch_phosphate

    Acetylated distarch phosphate, E1414 in the E number scheme of food additives, is a modified starch. These are not absorbed intact by the gut, but are significantly hydrolysed by intestinal enzymes and then fermented by intestinal microbiota .

  6. Alkyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Alkyl_phosphate

    For example, the formula of methyl phosphate is CH 3-H 2 PO 4, dimethyl phosphate – (CH 3) 2 HPO 4 and trimethyl phosphate – (CH 3) 3 PO 4. Alkyl phosphates are widely distributed in nature, and form the basis of most biological processes. For example, high energy metabolites such as ATP and PEP are alkyl phosphates, as are nucleic acids ...

  7. Nucleoside phosphoramidite - Wikipedia

    en.wikipedia.org/wiki/Nucleoside_phosphoramidite

    More recently, Ac (acetyl) group is often used to protect C and dC as shown in Figure. [27] In the second, mild protection scheme, A and dA are protected with isobutyryl [28] or phenoxyacetyl groups (PAC). [29] C and dC bear acetyl protection, [27] and G and dG are protected with 4-isopropylphenoxyacetyl (i-Pr-PAC) [30] or dimethylformamidino ...

  8. Mevalonate pathway - Wikipedia

    en.wikipedia.org/wiki/Mevalonate_pathway

    Mevalonate pathway diagram showing the conversion of acetyl-CoA into isopentenyl pyrophosphate, the essential building block of all isoprenoids. The eukaryotic variant is shown in black. Archaeal variants are shown in red and blue.

  9. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    Acetyl-CoA, the most common derivative, serves as an acyl donor in many biosynthetic transformations. Such acyl compounds are thioesters. Names of acyl groups of amino acids are formed by replacing the -ine suffix with -yl.