The 2-propenyl-4,5-dihydroxycyclopent-2-enones 4, 10 and 14 have been synthesised in optically active form. NMR data suggest the compounds 10 and 14 (but not 4) correspond to compounds isolated from ascomycete strain A23-98. © 2004 Elsevier Ltd. All rights reserved.
Bickley, J., Roberts, J.e., Santoro, M.g., Snape, T. (2004). Synthesis and revision of the stereochemistry of a cyclopentenone natural product isolated from ascomycete strain A23-98. TETRAHEDRON, 60(11), 2569-2576 [10.1016/j.tet.2004.01.045].
Synthesis and revision of the stereochemistry of a cyclopentenone natural product isolated from ascomycete strain A23-98
ROBERTS, JOHN ELIAS;SANTORO, MARIA GABRIELLA;
2004-01-01
Abstract
The 2-propenyl-4,5-dihydroxycyclopent-2-enones 4, 10 and 14 have been synthesised in optically active form. NMR data suggest the compounds 10 and 14 (but not 4) correspond to compounds isolated from ascomycete strain A23-98. © 2004 Elsevier Ltd. All rights reserved.File in questo prodotto:
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