2003
DOI: 10.1515/znc-2003-5-605
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Three Highly Oxygenated Caryophyllene Sesquiterpenes from Pestalotiopsis sp., a Fungus Isolated from Bark of Pinus taeda

Abstract: A Pestalotiopis sp. was isolated from the trunk bark of Pinus taeda. The fungus was cultivated in liquid medium and produced three highly oxygenated caryophyllene sequiterpene derivatives, named pestalotiopsolide A, taedolidol and 6-epitaedolidol, respectively. The sesquiterpenes were isolated by silica gel based chromatographic procedures and their structures were elucidated by NMR spectroscopic data.

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Cited by 31 publications
(27 citation statements)
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“…[14][15][16] This paper reports the isolation and structural elucidation of three anthraquinone derivatives, a new lactone (1) named guepinone, isosulochrin (2) and chloroisosulochrin (3), 17 Figure 1. In addition, this is the first report of P. guepinii as an endophyte from V. michelii and its production of anthraquinones derivatives.…”
Section: Introductionmentioning
confidence: 99%
“…[14][15][16] This paper reports the isolation and structural elucidation of three anthraquinone derivatives, a new lactone (1) named guepinone, isosulochrin (2) and chloroisosulochrin (3), 17 Figure 1. In addition, this is the first report of P. guepinii as an endophyte from V. michelii and its production of anthraquinones derivatives.…”
Section: Introductionmentioning
confidence: 99%
“…20 Therefore, 3 was assigned 1R, 2R, 5S, 6S, 8R, 9S, 10R, 11R, and 12S absolute configuration. Cytosporinols A-C (1-3) are closely related to the known taedolidol, 3 6-epitaedolidol, 3 and punctaporonin C (4), 7-9 all possessing the rare oxatetracyclo[6.3.2.0 1,4 .0 5,13 ]tridecane skeleton, but differ by having different substituents at C-6 (1), C-10 (1-3), and C-11 (3), as well as a tetrasubstituted olefin (1) and a terminal olefin (2). In addition, 1-3 are structurally similar to a synthetic byproduct 5 created in the acid-mediated cyclization of the nonatural enantiomer pestalotiopins, 23,24 but differ in having different configurations for all stereogenic centers and substituents at C-6 and C-11, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…In addition, 1-3 are structurally similar to a synthetic byproduct 5 created in the acid-mediated cyclization of the nonatural enantiomer pestalotiopins, 23,24 but differ in having different configurations for all stereogenic centers and substituents at C-6 and C-11, respectively. Biogenetically, 1-3 could be derived from co-isolated fuscoatrol A 5 as proposed for the cytosporolides, 16 first via addition and cyclization to form 6, an intermediate of the C-6 deacetylate of (+)-pestalotiopsin A, 1 and then the acidcatalyzed cyclizations of 6 via two intermediates 7 and 8 could afford the key putative intermediate 9, 23 from which 1-3, taedolidol, 3 6-epitaedolidol, 3 and punctaporonin C (4) 7-9 could be generated via different routes (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%
“…The structure was solved Table 3. 13 by direct methods using SHELXL-97 25 and refined using full-matrix least-squares difference Fourier techniques. All non-hydrogen atoms were refined with anisotropic displacement parameters, and all hydrogen atoms were placed in idealized positions and refined as riding atoms with the relative isotropic parameters.…”
Section: Methodsmentioning
confidence: 99%