Determination of the absolute configuration of yessotoxin, a polyether compound implicated in diarrhetic shellfish poisoning, by NMR spectroscopic method using a chiral anisotropic reagent, methoxy-(2-naphthyl)acetic acid
- 1 September 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (39) , 7087-7090
- https://doi.org/10.1016/0040-4039(96)01580-8
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- 2-Anthrylmethoxyacetic acid, a new chiral anisotropic reagent for elucidating the absolute configuration of acyclic alcoholsTetrahedron Letters, 1996
- New chiral anisotropic reagents for determining the absolute configuration of carboxylic acidsTetrahedron Letters, 1995
- Conformational Structure and Dynamics of Arylmethoxyacetates: DNMR Spectroscopy and Aromatic Shielding EffectThe Journal of Organic Chemistry, 1995
- Determination of the Absolute Configuration of Ginnol, a Long-chain Aliphatic Alcohol, by Use of a New Chiral Anisotropic ReagentChemistry Letters, 1994
- New chirality recognizing reagents for the determination of absolute stereochemistry and enantiomeric purity by NMRTetrahedron Letters, 1994
- Marine toxinsChemical Reviews, 1993
- High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoidsJournal of the American Chemical Society, 1991
- Isolation and structure of yessotoxin, a novel polyether compound implicated in diarrhetic shellfish poisoningTetrahedron Letters, 1987
- Isolation and structure of brevetoxin B from the "red tide" dinoflagellate Ptychodiscus brevis (Gymnodinium breve)Journal of the American Chemical Society, 1981
- Strategy for the synthesis of large peptides: An application to the total synthesis of human parathyroid hormone [hPTH(1–84)]Biopolymers, 1981