New Oblongolides Isolated from the Endophytic FungusPhomopsissp. fromMelilotus dentata from the Shores of the Baltic Sea (Q78232858)

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200500290

12 December 2019

title

New Oblongolides Isolated from the Endophytic FungusPhomopsissp. fromMelilotus dentata from the Shores of the Baltic Sea (English)

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200500290

12 December 2019

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3a-hydroxy-7,9b-dimethyl-5a,6,7,8,9,9a-hexahydro-3H-benzo[g][2]benzofuran-1-one

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3a,7-Dihydroxy-7,9b-dimethyl-3,5a,6,8,9,9a-hexahydrobenzo[g][2]benzofuran-1-one

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3a-hydroxy-7-(hydroxymethyl)-9b-methyl-5a,6,7,8,9,9a-hexahydro-3H-benzo[g][2]benzofuran-1-one

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7-hydroxy-7,9b-dimethyl-3a,5a,6,8,9,9a-hexahydro-3H-benzo[g][2]benzofuran-1-one

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4-[5-(1-Hydroxyethyl)furan-2-yl]-4-oxobutanoic acid

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5-Hydroxy-7,9b-dimethyl-3,5,5a,6,7,8,9,9a-octahydrobenzo[g][2]benzofuran-1-one

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8-Hydroxy-7,9b-dimethyl-3,3a,5a,6,7,8,9,9a-octahydrobenzo[g][2]benzofuran-1-one

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Qzpmjuuyirzjkd-uhfffaoysa-

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(1-Acetyl-1-butoxy-9b-methyl-3,3a,5a,6,7,8,9,9a-octahydrobenzo[e][2]benzofuran-7-yl)methyl acetate

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(9b-Methyl-1-oxo-3,3a,5a,6,7,8,9,9a-octahydrobenzo[e][2]benzofuran-7-yl)methyl acetate

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7-(Hydroxymethyl)-9b-methyl-3,3a,5a,6,7,8,9,9a-octahydrobenzo[g][2]benzofuran-1-one

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Ythvcrznsxhbak-uhfffaoysa-

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(1-Acetyl-1-hydroxy-9b-methyl-3,3a,5a,6,7,8,9,9a-octahydrobenzo[e][2]benzofuran-7-yl)methyl acetate

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7

Siegfried Draeger

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200500290

12 December 2019

8

Barbara Schulz

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200500290

12 December 2019

2

Karsten Krohn

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200500290

12 December 2019

author name string

Jingqiu Dai

1

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200500290

12 December 2019

Dietmar Gehle

3

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200500290

12 December 2019

Ines Kock

4

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200500290

12 December 2019

Ulrich Flörke

5

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12 December 2019

Hans-Jürgen Aust

6

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12 December 2019

Joachim Rheinheimer

9

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European Journal of Organic Chemistry

12 December 2019

publication date

September 2005

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16 September 2022

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12 December 2019

volume

2005

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12 December 2019

issue

18

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12 December 2019

page(s)

4009-4016

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X-ray Structure Determination, Absolute Configuration and Biological Activity of Phomoxanthone A

12 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Marine-derived fungi: a chemically and biologically diverse group of microorganisms

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https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Secondary metabolites from marine microorganisms: bacteria, protozoa, algae and fungi. Achievements and prospects

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Metabolic products of Phomopsis oblonga. Part 1. 3a,5a,6,7,8,9,9a,9b-Octahydro-7,9b-dimethylnaphtho[1,2-c]furan-1(3H)-one (oblongolide)

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Elm bark beetle boring and feeding deterrents from Phomopsis oblonga

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

6H-dibenzo[b,d]pyran-6-one derivatives from the cultured lichen mycobionts of Graphis spp. and their biosynthetic origin

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Metabolic products of Phomopsis oblonga. Part 2. Phomopsolide A and B, tiglic esters of two 6-substituted 5,6-dihydro-5-hydroxypyran-2-ones

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Biosynthesis of Some Curvularin-Type Metabolites by a Hybrid Strain ME 0005 Derived from Penicillium citreo-viride B. IFO 6200 and 4629

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https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

The identification of 24-methylene-24,25-dihydrolanosterol and other possible ergosterol precursors in Phycomyces blakesleeanus and Agaricus campestris

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Novel phytotoxins produced by the causal fungus of the shoot blight of larches.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Metabolites from fungi 15. New isocoumarins from an endophytic fungus isolated from the Canadian thistle Cirsium arvense

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https://api.crossref.org/works/10.1002%2FEJOC.200500290

7 January 2021

Identifiers

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