(Q105120256)

English

Hemivannusal and Prevannusadials – New Sesquiterpenoids from the Marine Ciliate ProtistEuplotes vannus: The Putative Biogenetic Precursors of Dimeric Terpenoid Vannusals

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scholarly article

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Hemivannusal and Prevannusadials – New Sesquiterpenoids from the Marine Ciliate ProtistEuplotes vannus: The Putative Biogenetic Precursors of Dimeric Terpenoid Vannusals (English)

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

Euplotes vannus

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(5R)-2-(hydroxymethyl)-5-[(2S)-6-methyl-1-oxohept-5-en-2-yl]cyclopentene-1-carbaldehyde

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Prevannusadial A

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(3S)-3alpha-(2-Oxo-3alpha-isopropylcyclopentane-1beta-yl)-1-(acetoxymethyl)cyclopentene-2-carbaldehyde

1 reference

6-(2-Hydroxyethylidene)-2-(4-methylpent-3-enyl)hept-2-enedial

1 reference

author name string

Graziano Guella

1

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

Emanuela Callone

2

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

Graziano Di Giuseppe

3

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

Rita Frassanito

4

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

Francesco P. Frontini

5

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

Ines Mancini

6

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

Fernando Dini

7

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

publication date

November 2007

1 reference

16 September 2022

European Journal of Organic Chemistry

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

2007

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

31

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

5226-5234

1 reference

http://api.crossref.org/works/10.1002%2Fejoc.200700455

Preuplotin, a putative biogenetic precursor of the euplotins, bioactive sesquiterpenoids of the marine ciliated protist Euplotes crassus

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Antimicrobial activity of euplotin C, the sesquiterpene taxonomic marker from the marine ciliate Euplotes crassus

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytotoxic effects and apoptotic signalling mechanisms of the sesquiterpenoid euplotin C, a secondary metabolite of the marine ciliate Euplotes crassus, in tumour cells

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Raikovenal, a new sesquiterpenoid favouring adaptive radiation of the marine ciliate Euplotes raikovi, and its putative biogenetic precursor, preraikovenal

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

From Epiraikovenal, an Instrumental Niche-Exploitation Sesquiterpenoid of Some Strains of the Marine Ciliated Protisteuplotes raikovi, to an unusual intramoleculartele-dienone-olefin [2+2] photocycloaddition

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Rarisetenolide, Epoxyrarisetenolide, and Epirarisetenolide, New-Skeleton Sesquiterpene Lactones as Taxonomic Markers and Defensive Agents of the Marine Ciliated MorphospeciesEuplotes rariseta

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Epoxyfocardin and Its Putative Biogenetic Precursor, Focardin, Bioactive, New-Skeleton Diterpenoids of the Marine CiliateEuplotes focardii from Antractica

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthesis of (Z)-2-acyl-2-enals via retrocycloadditions of 5-acyl-4-alkyl-4H-1,3-dioxins: application in the total synthesis of the cytotoxin (+/-)-euplotin A

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

A catalytic asymmetric three-component 1,4-addition/aldol reaction: enantioselective synthesis of the spirocyclic system of vannusal A

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Bioactive terpenoids from caribbean marine algae of the genera penicillus and udotea (chlorophyta)

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Petiodial, a new monocyclic diterpenoid from the Mediterranean green algaUdotea petiolata

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Udoteal, a linear diterpenoid feeding deterrent from the tropical green alga Udotea flabellum

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Density-functional thermochemistry. III. The role of exact exchange

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Self‐consistent molecular orbital methods. XX. A basis set for correlated wave functions

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

Contracted Gaussian basis sets for molecular calculations. I. Second row atoms, Z=11–18

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700455

7 January 2021

based on heuristic

inferred from DOI database lookup

An expedient entry into the fused polycyclic skeleton of vannusal AElectronic supplementary information (ESI) available: selected physical data for compounds 11 and 2. See http://www.rsc.org/suppdata/cc/b2/b208234a/Dedicated to Professor Herbert C.

1 reference

9 March 2024

https://opencitations.net/index/api/v1/references/10.1002/EJOC.200700455

Identifiers

10.1002/EJOC.200700455

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