April 1, 1992Journal of the American Oil Chemists Society

7,10‐Dihydroxy‐8(E)‐Octadecenoic acid: Stereochemistry and a novel derivative, 7,10‐Dihydroxyoctadecanoic acid

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GKGerhard KnotheAgricultural Research Service MBM. O. BagbyUnited States Department of Agriculture RPRobert E. PetersonUniversity of Tennessee at Knoxville

Abstract

7,10‐Dihydroxy‐8(E)‐octadecenoic acid (obtained by bioconversion of oleic acid with the bacterial strain PR3) was hydrogenated with hydrazine hydrate under air in ethanolic solution to give a novel compound, 7,10‐dihydroxy‐octadecanoic acid. The absolute configuration of both compounds was determined with the aid of circular dichroism to be R,R. A different purification method for 7,10‐dihydroxy‐8(E)‐octadecenoic acid is described.

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Knothe et al. (1992) studied this question.

synapsesocial.com/papers/6aa2077ac187e7ea83ef9cbe https://doi.org/10.1007/bf02636070

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7,10‐Dihydroxy‐8(E)‐Octadecenoic acid: Stereochemistry and a novel derivative, 7,10‐Dihydroxyoctadecanoic acid

Abstract

Discussion

Cite This Study

7,10‐Dihydroxy‐8(E)‐Octadecenoic acid: Stereochemistry and a novel derivative, 7,10‐Dihydroxyoctadecanoic acid

Abstract

Discussion

Cite This Study

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