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Connection of Isolated Stereoclusters by Combining 13 C-RCSA, RDC, and J -Based Configurational Analyses and Structural Revision of a Tetraprenyltoluquinol Chromane Meroterpenoid from Sargassum muticum.

Authors :
Fuentes-Monteverde, Juan Carlos C.
Nath, Nilamoni
Forero, Abel M.
Balboa, Elena M.
Navarro-Vázquez, Armando
Griesinger, Christian
Jiménez, Carlos
Rodríguez, Jaime
Source :
Marine Drugs; Jul2022, Vol. 20 Issue 7, p462-462, 17p
Publication Year :
2022

Abstract

The seaweed Sargassum muticum, collected on the southern coast of Galicia, yielded a tetraprenyltoluquinol chromane meroditerpene compound known as 1b, whose structure is revised. The relative configuration of 1b was determined by J-based configurational methodology combined with an iJ/DP4 statistical analysis and further confirmed by measuring two anisotropic properties: carbon residual chemical shift anisotropies (<superscript>13</superscript>C-RCSAs) and one-bond <superscript>1</superscript>H-<superscript>13</superscript>C residual dipolar couplings (<superscript>1</superscript>D<subscript>CH</subscript>-RDCs). The absolute configuration of 1b was deduced by ECD/OR/TD-DFT methods and established as 3R,7S,11R. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16603397
Volume :
20
Issue :
7
Database :
Complementary Index
Journal :
Marine Drugs
Publication Type :
Academic Journal
Accession number :
158266995
Full Text :
https://doi.org/10.3390/md20070462