the Fischer projection, devised by Emil Fischer in 1891, is a two-dimensional representation of a three-dimensional organic molecule by projection. Fischer...
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Structural formula (redirect from Sawhorse projection)
formulas, skeletal formulas, Newman projections, Cyclohexane conformations, Haworth projections, and Fischer projections. Several systematic chemical naming...
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three-dimensional object Fischer projection, a two-dimensional representation of a three-dimensional organic molecule Haworth projection, a way of writing a...
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Nobel Prize in Chemistry. He discovered the Fischer esterification. He also developed the Fischer projection, a symbolic way of drawing asymmetric carbon...
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This projection is named after American chemist Melvin Spencer Newman, who introduced it in 1952 as a partial replacement for Fischer projections, which...
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below the plane of the ring in Haworth projections correspond to those on the right-hand side of a Fischer projection. This rule does not apply to the groups...
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or "L-", depending on whether the hydroxyl in position 5, in the Fischer projection of the molecule, is to the right or to the left of the axis, respectively...
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Monosaccharide (section Haworth projection)
bounded by 2c, where c is the total number of chiral carbons. The Fischer projection is a systematic way of drawing the skeletal formula of an acyclic...
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with all of its hydroxyl functional groups on the same side in its Fischer projection. d-Ribose has these hydroxyl groups on the right hand side and is...
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convention. A Fischer projection can be used to differentiate between L- and D- molecules Chirality (chemistry). For instance, by definition, in a Fischer projection...
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regular chiral atoms. See: Fischer projection Construction of the Fischer projection D-glucose in the Fischer projection. Red: Group with highest priority...
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carbon in the chain. Aldoses with alcohol groups on the right of the Fischer projection are D-aldoses, and those with alcohols on the left are L-aldoses....
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in α-D-glucopyranose the reference atom is C-5. If in the cyclic Fischer projection the exocyclic oxygen atom at the anomeric centre is cis (on the same...
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Wedge-and-dash notation in skeletal formulas Haworth projection Newman projection Fischer projection Dietrich Braun; Harald Cherdron; Matthias Rehahn; H. Ritter;...
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designate the relative configuration of the centers". As is depicted in a Fischer projection of D-threose, the adjacent substituents will have a syn orientation...
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asymmetric carbon furthest from the carbonyl group: in a standard Fischer projection if the hydroxyl group is on the right the molecule is a D sugar, otherwise...
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in deoxyribose all the hydroxyl groups are on the same side in the Fischer projection. The term "2-deoxyribose" may refer to either of two enantiomers:...
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inventor of the Fischer projection Horst Fischer (1912–1966), German SS concentration camp doctor executed for war crimes Howard Fischer, curator of the...
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acid can exist as any of three stereoisomers depicted below in a Fischer projection. Of the four colored pictures at the top of the diagram, the first...
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yield the same aldaric acid (this can be understood by looking at the Fischer projection of a sugar upside down—with normal aldoses, this is a different compound...
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drawing. Other types of representation, such as Newman projection, Haworth projection or Fischer projection, also look somewhat similar to skeletal formulae...
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as the Calvin cycle. The intermediates of glycolysis depicted in Fischer projections show the chemical changing step by step. Such image can be compared...
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threo and erythro. In the case of saccharides, when drawn in the Fischer projection the erythro isomer has two identical substituents on the same side...
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same molecular graph may exist as two or more stereoisomers. The Fischer projection is a systematic way of drawing the skeletal formula of an open-chain...
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l-Glucose Haworth projection of α-l-glucopyranose Fischer projection of α-l-glucose Names IUPAC name l-Glucose Identifiers CAS Number 921-60-8 Y 3D model...
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understanding occurred largely as a result of the investigations of Emil Fischer, a German chemist who received the 1902 Nobel Prize in Chemistry for his...
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position of these atoms in the molecule to be described unambiguously. A Fischer projection is a simplified way to depict the stereochemistry around a stereocenter...
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of glycerol (2-sn) is on the left on a Fischer projection. The numbering follows the one of Fischer's projections, being 1-sn the carbon at the top and...
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Berthelot renamed it "galactose" or "glucose lactique". In 1894, Emil Fischer and Robert Morrell determined the configuration of galactose. Galactogen...
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