New Bioactive 2,3-Epoxycyclohexenes and Isocoumarins from the Endophytic FungusPhomopsissp. fromLaurus Azorica (Q53606469)

5,8-Dihydroxy-3-propyl-3,4-dihydroisochromen-1-one

1 reference

1 reference

1 reference

6-Chloro-5,8-dihydroxy-3-propyl-3,4-dihydroisochromen-1-one

1 reference

5-propyl-2,3,5,6,7,7a-hexahydro-1aH-oxireno[2,3-g]isochromene-2,6,7-triol

1 reference

(1aS,2R,5R,6S,7S,7aR)-2,6,7-trihydroxy-5-propyl-1a,2,5,6,7,7a-hexahydrooxireno[2,3-g]isochromen-3-one

1 reference

(1aS,2R,5R,6R,7S,7aR)-2,6,7-trihydroxy-5-propyl-1a,2,5,6,7,7a-hexahydrooxireno[2,3-g]isochromen-3-one

1 reference

1 reference

1 reference

1 reference

Tibor Kurtán

8

0 references

Gennaro Pescitelli

Gennaro Pescitelli

5

0 references

Hidayat Hussain

Hidayat Hussain

1

0 references

Siegfried Draeger

3

Siegfried Draeger

0 references

Barbara Schulz

4

Barbara Schulz

0 references

Karsten Krohn

9

Karsten Krohn

0 references

author name string

Nadeem Akhtar

2

0 references

Piero Salvadori

6

0 references

Sándor Antus

European Journal of Organic Chemistry

7

0 references

publication date

February 2009

1 reference

16 September 2022

0 references

volume

2009

0 references

issue

5

0 references

page(s)

749-756

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

Dinemasones A, B and C - New Bioactive Metabolites from the Endophytic FungusDinemasporium strigosum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Metabolites from the endophytic fungus Phomopsis sp. PSU-D15.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Phomoxanthones A and B, novel xanthone dimers from the endophytic fungus Phomopsis species

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Biologically Active Metabolites from Fungi 61);Phomosines A-CThree New Biaryl Ethers fromPhomopsissp

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Novel Highly Substituted Biraryl Ethers, Phomosines D-G, Isolated from the Endophytic FungusPhomopsis sp. fromAdenocarpus foliolosus

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Phomopsichalasin, a novel antimicrobial agent from an endophytic Phomopsis sp.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Six new 10-pheynl-[11]cytochalasans, cytochalasins N - S from phomopsis SP.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Phytotoxic metabolites of Phomopsisconvolvulus, a host-specific pathogen of field bindweed

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Structure elucidation and absolute configuration of phomopsin a, a hexapeptide mycotoxin produced by phomopsis leptostromiformis

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Natural products from endophytic microorganisms

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

EI-1941-1 and -2, novel interleukin-1beta converting enzyme inhibitors produced by Farrowia sp. E-1941. I. Biochemical characterization of EI-1941-1 and -2.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

EI-1941-1 and -2, novel interleukin-1 beta converting enzyme inhibitors Produced by Farrowia sp. E-1941. II. Taxonomy of producing strain, fermentation, isolation, physico-chemical properties, and biological properties

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Structure elucidation of EI-1941-1 and -2, novel interleukin-1β converting enzyme inhibitors produced by Farrowia sp. E-1941

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Phaeofurans and sorbicillin analogues from a fungicolous Phaeoacremonium species (NRRL 32148).

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Isolation, structure, absolute stereochemistry, and HIV-1 integrase inhibitory activity of integrasone, a novel fungal polyketide.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Aromatic polyketides from marine algicolous fungi.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Bioactive Natural Products from the Endophytic FungusAscochyta sp. from Meliotus dentatus – Configurational Assignment by Solid-State CD and TDDFT Calculations

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

A chemical/computational approach to the determination of absolute configuration of flexible and transparent molecules: aliphatic diols as a case study

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Inherent chirality dominates the visible/near-ultraviolet CD spectrum of rhodopsin

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

The prediction of the circular dichroism of the benzene chromophore: TDDFT calculations and sector rules

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Synthesis, structure, and spectroscopic properties of chiral oxorhenium(V) complexes incorporating polydentate ligands derived from L-amino acids: a density functional theory/time-dependent density functional theory investigation

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Assignment of the absolute configuration of zwitterionic and neutral macropodumines by means of TDDFT CD calculations

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Dihydroisocoumarin from Xyris pterygoblephara active against dermatophyte fungi

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Dihydroisocoumarins from fungi: isolation, structure elucidation, circular dichroism and biological activity.

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Prenylated flavanones from the twigs of Dorstenia mannii

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Anomalous Face-Selectivity in Sharpless Asymmetric Dihydroxylation of o-Allylbenzamides

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Enantioselective Synthesis of 3-Methylisochromans and Determination of Their Absolute Configurations by Circular Dichroism

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021

Density functional theory calculations of optical rotation: employment of ADZP and its comparison with other basis sets

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200801052

7 January 2021