(Q57517865)

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New chirality recognizing reagents for the determination of absolute stereochemistry and enantiomeric purity by NMR

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New chirality recognizing reagents for the determination of absolute stereochemistry and enantiomeric purity by NMR (English)

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E. Quiñoá

3

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Ricardo Riguera

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R. Riguera

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4

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author name string

J.M. Seco

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1

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Sh. Latypov

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2

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publication date

May 1994

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published in

Tetrahedron Letters

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volume

35

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issue

18

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page(s)

2921-2924

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cites work

Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

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

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Elucidation of the relative and absolute stereochemistry of lobatriene, a marine diterpene, by a modified Mosher method

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Viridoxins A and B: novel toxins from the fungus Metarhizium flavoviride

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Structure and energetics of ligand binding to proteins: Escherichia coli dihydrofolate reductase-trimethoprim, a drug-receptor system.

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.alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines

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10.1016/S0040-4039(00)76661-5

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(Q57517865)

New chirality recognizing reagents for the determination of absolute stereochemistry and enantiomeric purity by NMR

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