(Q57517776)

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The assignment of absolute configurations by NMR of arylmethoxyacetate derivatives: is this methodology being correctly used?

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The assignment of absolute configurations by NMR of arylmethoxyacetate derivatives: is this methodology being correctly used? (English)

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Emilio Quiñoá

2

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Ricardo Riguera

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Ricardo Riguera

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3

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José M. Seco

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1

object named as

José Manuel Seco

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publication date

July 2000

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published in

Tetrahedron: Asymmetry

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volume

11

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issue

13

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page(s)

2781-2791

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cites work

Correlation of configuration and fluorine-19 chemical shifts of .alpha.-methoxy-.alpha.-trifluoromethylphenyl acetate derivatives

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Determining factors in the assignment of the absolute configuration of alcohols by NMR. The use of anisotropic effects on remote positions

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The use of ethyl 2-(9-anthryl)-2-hydroxyacetate for assignment of the absolute configuration of carboxylic acids by 1H NMR

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Assignment of the Absolute Configuration of β-Chiral Primary Alcohols by NMR: Scope and Limitations

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Boc-Phenylglycine: The Reagent of Choice for the Assignment of the Absolute Configuration of α-Chiral Primary Amines by1H NMR Spectroscopy

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Assignment of the absolute configuration of alpha-chiral carboxylic acids by 1H NMR spectroscopy

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Are Both the (R)-and the (S)-MPA Esters Really Needed for the Assignment of the Absolute Configuration of Secondary Alcohols by NMR? The Use of a Single Derivative

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Complexation with Barium(II) Allows the Inference of the Absolute Configuration of Primary Amines by NMR

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9-Anthrylmethoxyacetic acid esterification shifts—Correlation with the absolute stereochemistry of secondary alcohols

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Scanlonenyne, A Novel Halogenated C15 Acetogenin From The Red Alga Laurencia Obtusa In Irish Waters

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New Type of Mono-tetrahydrofuran Ring Acetogenins fromGoniothalamus donnaiensis

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4-deoxyannomontacin and (2,4-cis and trans)-annomontacinone, new bioactive mono-tetrahydrofuran annonaceous acetogenins from Goniothalamus giganteus.

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Conformational Structure and Dynamics of Arylmethoxyacetates: DNMR Spectroscopy and Aromatic Shielding Effect

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10.1016/S0957-4166(00)00228-7

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(Q57517776)

The assignment of absolute configurations by NMR of arylmethoxyacetate derivatives: is this methodology being correctly used?

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