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  2. 1,3-Bisphosphoglyceric acid - Wikipedia

    en.wikipedia.org/wiki/1,3-Bisphosphoglyceric_acid

    1,3-Bisphosphoglyceric acid (1,3-Bisphosphoglycerate or 1,3BPG) is a 3-carbon organic molecule present in most, if not all, living organisms.It primarily exists as a metabolic intermediate in both glycolysis during respiration and the Calvin cycle during photosynthesis. 1,3BPG is a transitional stage between glycerate 3-phosphate and glyceraldehyde 3-phosphate during the fixation/reduction of ...

  3. Organic acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Organic_acid_anhydride

    An acid anhydride is a compound that has two acyl groups bonded to the same oxygen atom. [1] A common type of organic acid anhydride is a carboxylic anhydride, where the parent acid is a carboxylic acid, the formula of the anhydride being (RC(O)) 2 O. Symmetrical acid anhydrides of this type are named by replacing the word acid in the name of ...

  4. Space-filling model of the 1,3-bisphosphoglyceric acid molecule, a biological intermediate present in most, if not all, living organisms. Used colors: Carbon, C: black

  5. C3H8O10P2 - Wikipedia

    en.wikipedia.org/wiki/C3H8O10P2

    1,3-Bisphosphoglyceric acid (1,3-BPG) 2,3-Bisphosphoglyceric acid (2,3-BPG) This page was last edited on 23 May 2021, at 01:33 (UTC). Text is available under the ...

  6. Organozinc chemistry - Wikipedia

    en.wikipedia.org/wiki/Organozinc_chemistry

    The reaction produces a primary, secondary, or tertiary alcohol via a 1,2-addition. The Barbier reaction is advantageous because it is a one-pot process: the organozinc reagent is generated in the presence of the carbonyl substrate. Organozinc reagents are also less water sensitive, thus this reaction can be conducted in water.

  7. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    The Knorr pyrrole synthesis is a widely used chemical reaction that synthesizes substituted pyrroles (3). [1] [2] [3] The method involves the reaction of an α-amino-ketone (1) and a compound containing an electron-withdrawing group (e.g. an ester as shown) α to a carbonyl group (2). [4] The Knorr pyrrole synthesis

  8. Zinc compounds - Wikipedia

    en.wikipedia.org/wiki/Zinc_compounds

    The composition of this layer can be complex, but one constituent is probably basic zinc carbonate, Zn 5 (OH) 6 CO 3. [8] The reaction of zinc with water is slowed by this passive layer. When this layer is corroded by acids such as hydrochloric acid and sulfuric acid, the reaction proceeds with the evolution of hydrogen gas. [1] [9] Zn + 2 H ...

  9. Bisphosphoglycerate phosphatase - Wikipedia

    en.wikipedia.org/wiki/Bisphosphoglycerate...

    The systematic name of this enzyme class is 2,3-bisphospho-D-glycerate 2-phosphohydrolase. Other names in common use include 2,3-diphosphoglycerate phosphatase , diphosphoglycerate phosphatase , 2,3-diphosphoglyceric acid phosphatase , 2,3-bisphosphoglycerate phosphatase , and glycerate-2,3-diphosphate phosphatase .