Investigation of the early stages in soraphen A biosynthesis
Literature Information
Publication Date
2003-05-19
DOI
10.1039/B303542P
Impact Factor
6.222
Authors
Alison M. Hill, Betty L. Thompson, Jonathan P. Harris, Roger Segret
View Original
Abstract
The unusual benzoate starter unit in soraphen A derives from phenylalanine via cinnamate in a β-oxidative (plant-like) pathway; 3-phenyl-3-hydroxypropanoate incorporates directly into soraphen by loading onto module 2 of the PKS and indirectly from the β-oxidative pathway to generate benzoyl CoA.
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Source Journal
Chemical Communications
CiteScore:
8.6
Self-citation Rate:
4.7%
Articles per Year:
2458
ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry
Recommended Compounds
(2R,2'R)-1,1'-Bis(2-pyridinylmethyl)-2,2'-bipyrrolidine tetrahydrochloride
CAS Number:
1228077-88-0
Molecular Formula:
C20H30Cl4N4
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