the Fischer projection, devised by Emil Fischer in 1891, is a two-dimensional representation of a three-dimensional organic molecule by projection. Fischer...

formulas, skeletal formulas, Newman projections, Cyclohexane conformations, Haworth projections, and Fischer projections. Several systematic chemical naming...

three-dimensional object Fischer projection, a two-dimensional representation of a three-dimensional organic molecule Haworth projection, a way of writing a...

Nobel Prize in Chemistry. He discovered the Fischer esterification. He also developed the Fischer projection, a symbolic way of drawing asymmetric carbon...

This projection is named after American chemist Melvin Spencer Newman, who introduced it in 1952 as a partial replacement for Fischer projections, which...

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...

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...

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...

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...

convention. A Fischer projection can be used to differentiate between L- and D- molecules Chirality (chemistry). For instance, by definition, in a Fischer projection...

regular chiral atoms. See: Fischer projection Construction of the Fischer projection D-glucose in the Fischer projection. Red: Group with highest priority...

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....

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...

Wedge-and-dash notation in skeletal formulas Haworth projection Newman projection Fischer projection Dietrich Braun; Harald Cherdron; Matthias Rehahn; H. Ritter;...

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...

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...

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:...

Fischer projection of meso-tartaric acid...

inventor of the Fischer projection Horst Fischer (1912–1966), German SS concentration camp doctor executed for war crimes Howard Fischer, curator of the...

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...

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...

drawing. Other types of representation, such as Newman projection, Haworth projection or Fischer projection, also look somewhat similar to skeletal formulae...

as the Calvin cycle. The intermediates of glycolysis depicted in Fischer projections show the chemical changing step by step. Such image can be compared...

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...

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...

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...

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...

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...

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...

Berthelot renamed it "galactose" or "glucose lactique". In 1894, Emil Fischer and Robert Morrell determined the configuration of galactose. Galactogen...