(Q56608861)

(3-Methylidene-1-benzoxepin-7-yl)methyl octadec-9-enoate

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[(3E)-3-(chloromethylidene)-1-benzoxepin-7-yl]methyl (Z)-octadec-9-enoate

1 reference

[(3Z)-3-(chloromethylidene)-1-benzoxepin-7-yl]methyl (9Z,12Z)-octadeca-9,12-dienoate

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3-[(E)-Chloromethylene]-2,3-dihydro-1-benzoxepin-7-methanol

1 reference

(3-Methylidene-1-benzoxepin-7-yl)methyl octadeca-9,12-dienoate

1 reference

[3-(Chloromethylidene)-1-benzoxepin-7-yl]methyl octadeca-9,12-dienoate

1 reference

{(E)-3-(Chloromethylene)-2,3-dihydrobenzo[b]oxepin-7-yl}methylPalmitate

1 reference

[(3E)-3-(chloromethylidene)-1-benzoxepin-7-yl]methyl (Z)-hexadec-9-enoate

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[3-(Chloromethylidene)-1-benzoxepin-7-yl]methyl hexadec-9-enoate

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(3-methylidene-1-benzoxepin-7-yl)methyl (Z)-octadec-9-enoate

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[3-(Chloromethylidene)-1-benzoxepin-7-yl]methyl octadecanoate

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[3-(Chloromethylidene)-1-benzoxepin-7-yl]methyl octadec-9-enoate

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[3-(Chloromethylidene)-6-hydroxy-1-benzoxepin-7-yl]methyl hexadecanoate

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[(3Z)-3-(chloromethylidene)-1-benzoxepin-7-yl]methyl (Z)-hexadec-9-enoate

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[3-(Chloromethylene)-2,3-dihydro-1-benzoxepin-7-yl]methanol

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3-[(Z)-Chloromethylene]-7-(palmitoyloxymethyl)-2,3-dihydro-1-benzooxepin

1 reference

[(3E)-3-(chloromethylidene)-1-benzoxepin-7-yl]methyl (9Z,12Z)-octadeca-9,12-dienoate

1 reference

[(3Z)-3-(chloromethylidene)-2H-1-benzoxepin-7-yl]methyl (9Z)-octadec-9-enoate

1 reference

[3-(Chloromethylidene)-1-benzoxepin-7-yl]methyl hexadecanoate

1 reference

[(3E)-3-(chloromethylidene)-1-benzoxepin-7-yl]methyl octadecanoate

1 reference

3-[(E)-Chloromethylene]-7-(palmitoyloxymethyl)-2,3-dihydro-1-benzooxepin

1 reference

(3-Methylidene-1-benzoxepin-7-yl)methyl octadecanoate

1 reference

(3-methylidene-1-benzoxepin-7-yl)methyl (9Z,12Z)-octadeca-9,12-dienoate

1 reference

[3-(Chloromethylidene)-1-benzoxepin-7-yl]methoxy-trimethylsilane

1 reference

{[(3Z)-3-(chloromethylidene)-2H-1-benzoxepin-7-yl]methoxy}trimethylsilane

1 reference

3-(Chloromethylene)-2,3-dihydro-1-benzooxepin-7-methanol

1 reference

3

Peter Spiteller

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author name string

Silke Peters

series ordinal

1

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Robert J. R. Jaeger

series ordinal

2

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publication date

March 2008

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16 September 2022

European Journal of Organic Chemistry

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volume

2008

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issue

7

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page(s)

1187-1194

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cites work

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Sanguinones A and B, blue pyrroloquinoline alkaloids from the fruiting bodies of the mushroom Mycena sanguinolenta

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1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700812

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Red Pyrroloquinoline Alkaloids from the MushroomMycena haematopus

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https://api.crossref.org/works/10.1002%2FEJOC.200700812

7 January 2021

Mycenarubins A and B, Red Pyrroloquinoline Alkaloids from the MushroomMycena rosea

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https://api.crossref.org/works/10.1002%2FEJOC.200700812

7 January 2021

Novel monochlorinated metabolites with a 1-benzoxepin skeleton from Mycena galopus

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https://api.crossref.org/works/10.1002%2FEJOC.200700812

7 January 2021

Total synthesis and bioactivity of some naturally occurring pterulones

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https://api.crossref.org/works/10.1002%2FEJOC.200700812

7 January 2021

Pterulinic acid and pterulone, two novel inhibitors of NADH:ubiquinone oxidoreductase (complex I) produced by a Pterula species. II. Physico-chemical properties and structure elucidation

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7 January 2021

Effects of feeding Spodoptera littoralis on lima bean leaves. II. Continuous mechanical wounding resembling insect feeding is sufficient to elicit herbivory-related volatile emission

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7 January 2021

Octadecanoid Precursors of Jasmonic Acid Activate the Synthesis of Wound-Inducible Proteinase Inhibitors

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https://api.crossref.org/works/10.1002%2FEJOC.200700812

7 January 2021

The octadecanoic pathway: signal molecules for the regulation of secondary pathways

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7 January 2021

New aspects of amanitin and phalloidin poisoning.

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7 January 2021

Amatoxins, Phallotoxins, Phallolysin, and Antamanide: The Biologically Active Components of PoisonousAmanitaMushroom

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7 January 2021

Amanita muscaria: chemistry, biology, toxicology, and ethnomycology

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7 January 2021

New benzodioxepin type strobilurins from basidiomycetes. Structural revision and determination of the absolute configuration of strobilurin D and related β-methoxyacrylate antibiotics

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7 January 2021

Die chemische Verteidigung des RindenpilzesAleurodiscus amorphus mithilfe eines maßgeschneiderten, Blausäure freisetzenden Cyanhydrinethers

1 reference

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7 January 2021

Pilzfarbstoffe, 60 Über Leucomentine, farblose Vorstufen des Atromentins aus dem Samtfußkrempling (Paxillus atrotomentosus)

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700812

7 January 2021

Pilzfarbstoffe, 61 Flavomentine und Spiromentine, neue Terphenylchinon-Derivate aus Paxillus atrotomentosus und P. panuoides (Boletales)

1 reference

https://api.crossref.org/works/10.1002%2FEJOC.200700812

7 January 2021

The sesquiterpenes of Lactarius deliciosus and Lactarius deterrimus

1 reference

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7 January 2021