(Q104415121)

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Absolute configuration assignments by experimental and theoretical approaches of ent-labdane- and cis-ent-clerodane-type diterpenes isolated from Croton glabellus

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scholarly article

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Absolute configuration assignments by experimental and theoretical approaches of ent-labdane- and cis-ent-clerodane-type diterpenes isolated from Croton glabellus (English)

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Croton glabellus

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beta-sitosterol

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(1S,8aalpha)-3,4abeta,8,8-Tetramethyl-4beta-[(E)-3-methyl-2,4-pentadienyl]-1alpha,2beta,3alpha-decalintriol 1-acetate

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trans-Dehydrocrotonin

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(1S,8aalpha)-1alpha,2beta-[Isopropylidenebis(oxy)]-3,4abeta,8,8-tetramethyl-4beta-[(E)-3-methyl-2,4-pentadienyl]decalin-3alpha-ol

1 reference

(1R)-3,4,4',4aalpha,5',8abeta-Hexahydro-5'alpha-[(5R)-2,5-dihydro-5-hydroxy-2-oxofuran-3-yl]-2alpha,5-dimethylspiro[naphthalene-1(2H),3'(2'H)-furan]-2',7(8H)-dione

1 reference

3-methoxyapigenin

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(1S,2R,3R,4S,4aR,8aR)-3,4a,8,8-tetramethyl-4-[(2E)-3-methylpenta-2,4-dienyl]-2,4,5,6,7,8a-hexahydro-1H-naphthalene-1,2,3-triol

1 reference

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3',4',5,7-tetrahydroxy-3-methoxyflavone

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Guillermo Delgado

4

object named as

Guillermo Delgado

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http://api.crossref.org/works/10.1139%2Fv06-164

author name string

Abraham García

1

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http://api.crossref.org/works/10.1139%2Fv06-164

Teresa Ramírez-Apan

2

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http://api.crossref.org/works/10.1139%2Fv06-164

J Antonio Cogordan

3

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http://api.crossref.org/works/10.1139%2Fv06-164

publication date

1 December 2006

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16 September 2022

Canadian Journal of Chemistry

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http://api.crossref.org/works/10.1139%2Fv06-164

84

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http://api.crossref.org/works/10.1139%2Fv06-164

12

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http://api.crossref.org/works/10.1139%2Fv06-164

1593-1602

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http://api.crossref.org/works/10.1139%2Fv06-164

Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1093/JNCI/83.11.757

Über Marrubiasid und Marrubialacton, zwei Diterpenderivate mit umgelagertem Labdangerüst ausLeonurus marrubiastrum L.

1 reference

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/CBER.19731060923

Uncommon Sesquiterpenoids and New Triterpenoids fromJatropha neopauciflora (Euphorbiaceae)

1 reference

9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/HLCA.200690009

Antimicrobial flavonoids from Psiadia trinervia and their methylated and acetylated derivatives

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Insect growth inhibitory nor-diterpenes, cis-dehydrocrotonin and trans-dehydrocrotonin, from Croton cajucara

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Clerodane diterpenes from Baccharis sagittalis: insect antifeedant activity

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Diterpenoids from the stem bark of Croton zambesicus

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Nor-clerodane diterpenes from Croton cajucara

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Isolation of austroinulin possessing cell cycle inhibition activity from Blumea glomerata and revision of its absolute configuration

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Neo-clerodane insect antifeedants from Scutellaria galericulata

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Cajucarinolide and isocajucarinolide: anti-inflammatory diterpenes from Croton cajucara

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Beyerene derivatives and other terpenoids from Stevia aristata

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Labdane-type diterpenes from Stevia rebaudiana

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

cis-Clerodane Diterpene Lactones fromAmphiachyris dracunculoides. 2†

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1139/V06-164

Identifiers

10.1139/V06-164

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