(Q57517780)

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

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

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Emilio Quiñoá

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Ricardo Riguera

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Ricardo Riguera

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3

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author name string

JoséManuel Seco

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1

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publication date

January 1999

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published in

Tetrahedron

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volume

55

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page(s)

569-584

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issue

2

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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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Choosing the Right Reagent for the Determination of the Absolute Configuration of Amines by NMR: MTPA or MPA?†

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7 January 2021

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

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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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7 January 2021

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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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The unusual presence of hydroxylated furanosesquiterpenes in the deep ocean tunicate Ritterella rete. Chemical interconversions and absolute stereochemistry

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10.1016/S0040-4020(98)01055-2

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(Q57517780)

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

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