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Beilstein J. Org. Chem. 2018, 14, 900–910, doi:10.3762/bjoc.14.77
Graphical Abstract
Figure 1: Total ion chromatograms of headspace extracts from A) Aspergillus fischeri NRRL 181, B) Aspergillus...
Scheme 1: Volatiles from Aspergillus fischeri. For all chiral compounds in Schemes 1–5 the relative configura...
Scheme 2: Biosynthesis of bisabolanes and related terpenes in A. fischeri.
Scheme 3: Biosynthesis of daucanes in A. fischeri.
Scheme 4: Volatiles from A. kawachii. A) Proposed biosynthesis of sesquiterpenes, B) other identified volatil...
Scheme 5: Volatiles from A. clavatus.
Beilstein J. Org. Chem. 2014, 10, 1796–1801, doi:10.3762/bjoc.10.188
Figure 1: TDA and related natural products from Phaeobacter inhibens.
Scheme 1: Synthesis of tropone-2-carboxylic acid (13).
Scheme 2: Synthesis of halogenated TDA analogues.
Scheme 3: Further compounds included in this SAR study.
Beilstein J. Org. Chem. 2013, 9, 942–950, doi:10.3762/bjoc.9.108
Figure 1: Roseobacter clade metabolites.
Scheme 1: Degradation of DMSP via (A) demethylation pathway and (B) cleavage pathways. FH4: tetrahydrofolate.
Scheme 2: Sulfate reduction pathway and incorporation of sulfur into the amino acid pool. PAP: adenosine 3’,5...
Figure 2: Volatiles from P. gallaeciensis DSM 17395 and R. pomeroyi DSS-3. Feeding of [2H6]DMSP results in de...
Figure 3: Chromatograms of headspace extracts from P. gallaeciensis DSM 17395 after feeding of DMTeP by the u...
Figure 4: Chromatograms of headspace extracts obtained after feeding of [2H6]DMSP by the use of SPME from (A) ...
Figure 5: Chromatograms of headspace extracts from (A) R. pomeroyi DSS-3 wild type, (B) R. pomeroyi DSS-3 dmdA...
Scheme 3: Synthesis of 34S-labeled thiosulfate and sulfate.
Figure 6: Volatiles from P. gallaeciensis after feeding of selenate and selenite.
Figure 7: Chromatograms of headspace extracts from P. gallaeciensis grown on (A) 50% MB2216, (B) 50% MB2216 +...
Figure 8: Additional sulfur volatiles.