| Literature DB >> 22135237 |
Hui-Hui Tan1, Asami Makino, Kumar Sudesh, Peter Greimel, Toshihide Kobayashi.
Abstract
At a glance: The stereochemical configuration of the diglycerophosphate backbone of the endosome-specific lipid bis(monoacylglycero)phosphate (BMP, see picture) was determined by (1)H NMR spectroscopy. Enantiomeric discrimination was facilitated by introduction of D-camphor ketals as chiral shift reagents, and enantiopure synthetic BMP analogues were prepared as reference materials. Natural BMP exhibited the unusual sn-1,1' diglycerophosphate backbone.Entities:
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Year: 2011 PMID: 22135237 DOI: 10.1002/anie.201106470
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336