(Q104908842)

http://api.crossref.org/works/10.1002/hlca.19830660211

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1 reference

(1R)-4-[(1E,3E,5E,7E,9E,11E,13E,15Z,17E,19E)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol

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(1R)-4-[(1E,3E,5E,7Z,9E,11E,13E,15E,17E,19E)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol

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(1R)-4-[(1E,3E,5E,7E,9E,11Z,13E,15E,17E,19E)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol

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(1R,2R,4R)-1-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-2,6,6-trimethylcyclohexane-1,2,4-triol

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(18E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,16,18,22,26,30-nonaene

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15Z-β,β-carotene-3R,3R'-diol

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7',8'-Dihydro-psi,psi-carotene

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(2S,3aR,5R)-2-[(2E,4E,6E,8E,10E,12E,14E,16E)-17-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-6,11,15-trimethylheptadeca-2,4,6,8,10,12,14,16-octaen-2-yl]-7,7-dimethyl-2,3,3a,4,5,6-hexahydroinden-5-ol

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(8E,10E,12E,14E,16E,18E,20E,22E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,26,30-dodecaene

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(6Z,8E,10E,12E,14E,16E,18E,20E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,26,30-dodecaene

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2-(3,7,12,16,20,24-Hexamethylpentacosa-1,3,5,7,9,11,13,15,19,23-decaenyl)-1,3,3-trimethylcyclohexene

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(10E,12E,14E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,12,14,16,18,22,26,30-decaene

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2,6,10,14,19,23,27,31-Octamethyl 2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene

all-trans-phytofluene

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all-trans-zeta-carotene

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(1R)-4-[(1E,3E,5E,7Z,9E,11E,13E,15E,17E,19Z)-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol

1 reference

1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene

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Edith Märki-Fischer

1

1 reference

http://api.crossref.org/works/10.1002/hlca.19830660211

Urs Marti

series ordinal

2

1 reference

http://api.crossref.org/works/10.1002/hlca.19830660211

Richard Buchecker

series ordinal

3

1 reference

http://api.crossref.org/works/10.1002/hlca.19830660211

Conrad Hans Eugster

series ordinal

4

1 reference

http://api.crossref.org/works/10.1002/hlca.19830660211

publication date

16 March 1983

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16 September 2022

Helvetica Chimica Acta

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http://api.crossref.org/works/10.1002/hlca.19830660211

volume

66

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http://api.crossref.org/works/10.1002/hlca.19830660211

issue

2

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http://api.crossref.org/works/10.1002/hlca.19830660211

page(s)

494-513

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http://api.crossref.org/works/10.1002/hlca.19830660211

cites work

Studies in carotenogenesis. 19. A survey of the polyenes in a number of ripe berries

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https://api.crossref.org/works/10.1002/HLCA.19830660211

7 January 2021

THE CONFIGURATION OF PHYTOENE

1 reference

https://api.crossref.org/works/10.1002/HLCA.19830660211

7 January 2021

Die Carotinoide der Blüten vonRosa foetida

1 reference

https://api.crossref.org/works/10.1002/HLCA.19830660211

7 January 2021

Studies on carotenoids: Gazaniaxanthin

1 reference

https://api.crossref.org/works/10.1002/HLCA.19830660211

7 January 2021

Carotenoids of higher plants—II

1 reference

https://api.crossref.org/works/10.1002/HLCA.19830660211

7 January 2021

cis-trans Isomerization and Spectral Characteristics of Gazaniaxanthin. Further Evidence of its Structure

1 reference

https://api.crossref.org/works/10.1002/HLCA.19830660211

7 January 2021

Mimulaxanthin, Hauptcarotinoid vonLamium montanum, und seine absolute Konfiguration; konfigurative Verknüpfung von Deepoxyneoxanthin mit Neoxanthin

1 reference

https://api.crossref.org/works/10.1002/HLCA.19830660211

7 January 2021