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Stereochemical assignment

Determination of the spatial arrangement of atoms in a molecule.

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Articles of Stereochemical assignment

Studies on the synthesis of the quartromicins: Partial stereochemical assignment of quartromicins A₃ and D₃ and diastereoselective synthesis of the endo- and exo-spirotetronate subunits
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STEREOCHEMICAL ASSIGMENT BY MASS SPECTROMETRY. DOUBLE BOND GEOMETRICAL ISOMERS OF 3,5-DIALKYLCYCLOHEXYLIDENE ACETIC ACID ESTERS AND 3-ALKYL-2-ALKENOATES
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Site- and stereoselectivity in the photochemical oxetane formation reaction (Paterno-Buechi reaction) of tetrahydrobenzofuranols with benzophenone: hydroxy-directed diastereoselectivity?
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ASYMMETRIC SYNTHESIS XV: ENANTIOSPECIFIC SYNTHESIS OF (+) AND (-) ISONITRAMINES FROM A COMMON CHIRAL INTERMEDIATE.
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Total synthesis of (-)-blepharocalyxin D and analogues
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- methyl (2E,8E)-5-methyl-9-phenyl-4-oxanona-2,8-dienoate
Syntheses of Four Possible Diastereoisomers of Bohlmann's Structure of Isoepoxyestafiatin. The Stereochemical Assignment of Isoepoxyestafiatin
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- 3H-Oxireno[8,8a]azuleno[4,5-b]furan-8(4aH)-one,5,6,6a,7,9a,9b-hexahydro-1,4a,7-trimethyl-, (3aS,4aR,6aS,7S,9aS,9bR)- (9CI)

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Related entries

Oxidation Asymmetric synthesis Enantiomer Regioselectivity Diastereoselectivity Column chromatography Yield NMR spectroscopy Mass spectrometry HPLC Nucleophile Electrophile Reduction Enantiomeric excess (ee) Chromatography Recrystallization Catalytic hydrogenation Total synthesis Mass spectrometry (MS) Enantioselective synthesis Nucleophilic substitution Syntheses Cross-coupling Rotary evaporation PHOTOCHEMICAL REACTION Optical rotation Deprotection TLC (thin-layer chromatography) HPLC (high-performance liquid chromatography) Protecting group Benzophenone Diastereoisomers Resolution Anhydrous conditions Leaving group Diastereomers Catalytic asymmetric synthesis Stereocontrol Retrosynthetic analysis Asymmetric Induction Product Isolation Stereochemical Control Asymmetric Hydrogenation Chirality transfer Chiral Catalyst Stereoselectivity Cycloaddition Kinetic Resolution Oxidation/Reduction Chiral Auxiliary

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