(Q78233080)

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

title

Spicochalasin A and New Aspochalasins from the Marine-Derived FungusSpicaria elegans (English)

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

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Mariannaea elegans var. elegans

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5-Hydroxy-9,13,14-trimethyl-16-(2-methylpropyl)-17-azatricyclo[9.7.0.01,15]octadeca-9,12-diene-2,6,18-trione

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13-Hydroxy-1,5,6-trimethyl-8-(2-methylpropyl)-19-oxa-9-azapentacyclo[14.2.1.02,14.03,11.07,11]nonadec-4-ene-10,12,15-trione

1 reference

(3S,12E,16S)-2,3beta,12-Trimethyl-9alpha-hydroxy-16-isobutyl-4beta,4abeta-(methaniminomethano)-4,4a,5,8,9,10,11,13aalpha-octahydro-3H-benzocycloundecene-5,8,14-trione

1 reference

1 reference

9,13,14-Trimethyl-16-(2-methylpropyl)-3-(2-oxopropyl)-17-azatricyclo[9.7.0.01,15]octadeca-9,12-diene-2,5,18-trione

1 reference

6-Hydroxy-9,13,14-trimethyl-16-(2-methylpropyl)-17-azatricyclo[9.7.0.01,15]octadeca-9,12-diene-2,5,18-trione

1 reference

1 reference

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(1S,2R,3R,6S,7R,8S,11S,13R,14R,16R)-13-hydroxy-1,5,6-trimethyl-8-(2-methylpropyl)-19-oxa-9-azapentacyclo[14.2.1.02,14.03,11.07,11]nonadec-4-ene-10,12,15-trione

1 reference

(1R,5S,9E,11S,14S,15R)-5-hydroxy-9,13,14-trimethyl-15-[(1S)-3-methyl-1-(methylamino)butyl]-2,6-dioxobicyclo[9.4.0]pentadeca-9,12-diene-1-carbaldehyde

1 reference

1 reference

9,13,14-Trimethyl-16-(2-methylpropyl)-17-azatricyclo[9.7.0.01,15]octadeca-9,12-diene-2,5,18-trione

1 reference

1 reference

6-Hydroxy-9,13,14-trimethyl-16-(2-methylpropyl)-3-(2-oxopropyl)-17-azatricyclo[9.7.0.01,15]octadeca-9,12-diene-2,5,18-trione

1 reference

1 reference

Zhenjian Lin

1

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

Tianjiao Zhu

2

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

Hongjuan Wei

3

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

Guojian Zhang

4

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

Hui Wang

5

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

Qianqun Gu

6

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

European Journal of Organic Chemistry

12 December 2019

publication date

June 2009

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16 September 2022

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

volume

2009

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

issue

18

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

12 December 2019

page(s)

3045-3051

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085

The cytochalasans: a new class of biologically active microbial metabolites

12 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Molecular Basis of Cytochalasan Biosynthesis in Fungi: Gene Cluster Analysis and Evidence for the Involvement of a PKS-NRPS Hybrid Synthase by RNA Silencing

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7 January 2021

Alachalasins A-G, new cytochalasins from the fungus Stachybotrys Podospora vesticola [corrected].

1 reference

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7 January 2021

10-Phenyl-[12]-cytochalasins Z7, Z8, and Z9 from the marine-derived fungus Spicaria elegans.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Novel open-chain cytochalsins from the marine-derived fungus Spicaria elegans.

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https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Big effects from small changes: possible ways to explore nature's chemical diversity.

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7 January 2021

Aspergillin PZ, a novel isoindole-alkaloid from Aspergillus awamori.

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7 January 2021

Stoffwechselprodukte von Mikroorganismen. 186. Mitteilung. Über die Aspochalasine A, B, C und D

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https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Aspochalasin E, a new antibiotic isolated from a fungus

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https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Two new components of the aspochalasins produced by Aspergillus sp

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https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Structure of aspochalasin H, a new member of the aspochalasin family

1 reference

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7 January 2021

Aspochalasins I, J, and K: three new cytotoxic cytochalasans of Aspergillus flavipes from the rhizosphere of Ericameria laricifolia of the Sonoran Desert

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7 January 2021

A novel aspochalasin with HIV-1 integrase inhibitory activity from Aspergillus flavipes.

1 reference

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7 January 2021

Phomacins: Three Novel Antitumor Cytochalasan Constituents Produced by a Phoma sp.

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7 January 2021

Aspochalamins A-D and aspochalasin Z produced by the endosymbiotic Fungus aspergillus niveus LU 9575. I. Taxonomy, fermentation, isolation and biological activities.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

RKS-1778, a new mammalian cell-cycle inhibitor and a key intermediate of the [11]cytochalasin group

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Using jasplakinolide to turn on pathways that enable the isolation of new chaetoglobosins from Phomospis asparagi

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Discovery of aspoquinolones A-D, prenylated quinoline-2-one alkaloids from Aspergillus nidulans, motivated by genome mining

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Strategies to unravel the function of orphan biosynthesis pathways: recent examples and future prospects

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https://api.crossref.org/works/10.1002%2FEJOC.200801085

7 January 2021

Identifiers

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1002/ejoc.200801085