4.2 Article

New tricyclic and tetracyclic pyranocoumarins with an unprecedented C-4 substituent. Structure elucidation of tamanolide, tamanolide D and tamanolide P from Calophyllum inophyllum of French Polynesia

Journal

MAGNETIC RESONANCE IN CHEMISTRY
Volume 47, Issue 11, Pages 989-993

Publisher

WILEY
DOI: 10.1002/mrc.2482

Keywords

Calophyllum inophyllum; clusiaceae; pyranocoumarin; tamanolides; NMR; H-1 NMR; C-13 NMR; COSY; NOESY; HMQC; HMBC

Funding

  1. Delegation A la Recherche and MinistAMP
  2. re cle la Recherche of French Polynesia
  3. Ministere de I'Outre-Mer (MOM) of France

Ask authors/readers for more resources

Three new pyranocoumarin derivatives, tamanolide (1), tamanolide D (2) and tamanolide P (3), were isolated from the almond seeds of Calophyllum inophyllum L. (Clusiaceae) grown in French Polynesia. These compounds, having an unprecedented C-4 isobutyl substituent, have been characterized as a new class of pyranocoumarins called tamanolides. Their structures were elucidated on the basis of 1D and 2D NMR techniques (COSY, NOESY, HSQC and HMBC) in association with MS (HR-ESI-MS) data analysis. Copyright (C) 2009 John Wiley & Sons, Ltd.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available