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Enantiomeric Variability of Distaminolyne A. Refinement of ECD and NMR Methods for Determining Optical Purity of 1-Amino-2-Alkanols.


ABSTRACT: Sample configurations of distaminolyne A (1a); isolated from the ascidians Pseudodistoma opacum and P. cereum, and collected at different sites in New Zealand, were investigated by two methods: Exciton coupled electronic circular dichroism (EC ECD) of the corresponding N,O-dibenzoyl derivative 1b; and chiral reagent derivatization of 1a with (S)- and (R)-?-methoxyphenylacetic acid (MPA), followed by ¹H-NMR analysis. Configuration and optical purity of 1a (%ee) was found to vary depending on the geographic distribution of ascidian colonies. An improved method for preparing N,O-diarenoyl derivatives of 1a was optimized. The EC ECD method was found to be complementary to the MPA-NMR method at different ranges of %ee.

SUBMITTER: Pearce AN 

PROVIDER: S-EPMC6337674 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Enantiomeric Variability of Distaminolyne A. Refinement of ECD and NMR Methods for Determining Optical Purity of 1-Amino-2-Alkanols.

Pearce A Norrie AN   Copp Brent R BR   Molinski Tadeusz F TF  

Molecules (Basel, Switzerland) 20181227 1


Sample configurations of distaminolyne A (<b>1a</b>); isolated from the ascidians <i>Pseudodistoma opacum</i> and <i>P. cereum</i>, and collected at different sites in New Zealand, were investigated by two methods: Exciton coupled electronic circular dichroism (EC ECD) of the corresponding <i>N</i>,<i>O</i>-dibenzoyl derivative <b>1b</b>; and chiral reagent derivatization of <b>1a</b> with (<i>S</i>)- and (<i>R</i>)-α-methoxyphenylacetic acid (MPA), followed by ¹H-NMR analysis. Configuration and  ...[more]

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