Novel 24-nor-, 24-nor-2,3-seco-, and 3,24-dinor-2,4-seco-ursane triterpenes from Diospyros decandra: evidences for ring A biosynthetic transformations (Q105030336)

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scientific article published on 13 April 2006

Language	Label	Description	Also known as
English	Novel 24-nor-, 24-nor-2,3-seco-, and 3,24-dinor-2,4-seco-ursane triterpenes from Diospyros decandra: evidences for ring A biosynthetic transformations	scientific article published on 13 April 2006

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scholarly article

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Novel 24-nor-, 24-nor-2,3-seco-, and 3,24-dinor-2,4-seco-ursane triterpenes from Diospyros decandra: evidences for ring A biosynthetic transformations (English)

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

Diospyros decandra

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1,4,10-Trihydroxy-1,2,6a,6b,9,12a-hexamethyl-11-oxo-2,3,4,5,6,6a,7,8,8a,9,10,12,13,14b-tetradecahydropicene-4a-carboxylic acid

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1,10-Dihydroxy-1,2,6a,6b,9,12a-hexamethyl-11-oxo-2,3,4,5,6,6a,7,8,8a,9,10,12,13,14b-tetradecahydropicene-4a-carboxylic acid

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4-Oxo-19alpha,22alpha-dihydroxy-3,24-dinor-2,4-secours-12-ene-2,28-dioic acid

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methyl (2Z)-7,10-dihydroxy-2-(1-methoxy-1-oxopropan-2-ylidene)-1-(2-methoxy-2-oxoethyl)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydrochrysene-6a-carboxylate

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methyl (1R,2Z,4aR,4bS,6aS,7S,9R,10R,10aS,12aR)-7,10-dihydroxy-1-(2-methoxy-2-oxoethyl)-2-(1-methoxy-1-oxopropan-2-ylidene)-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydrochrysene-6a-carboxylate

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Lup-20(29)-en-28-oic acid, 3beta-hydroxy-

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2-Oxo-3beta,19alpha-dihydroxy-24-norurs-12-ene-28-oic acid

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1 reference

2-acetyl-1-(carboxymethyl)-7,10-dihydroxy-1,4a,4b,9,10-pentamethyl-3,4,5,6,7,8,9,10a,12,12a-decahydro-2H-chrysene-6a-carboxylic acid

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3-Oxo-2,19alpha,22alpha-trihydroxy-24-norurs-1,4,12-triene-28-oic acid

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2-Oxo-3beta,19alpha,22alpha-trihydroxy-24-norurs-12-ene-28-oic acid

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1,4,11-Trihydroxy-1,2,6a,6b,9,12a-hexamethyl-10-oxo-2,3,4,5,6,6a,7,8,13,14b-decahydropicene-4a-carboxylic acid

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author name string

Parichat Nareeboon

1

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

Wolfgang Kraus

2

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

Uwe Beifuss

3

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

Juergen Conrad

4

1 reference

http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

Iris Klaiber

5

1 reference

http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

Somyote Sutthivaiyakit

6

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

publication date

June 2006

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16 September 2022

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

62

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

5519-5526

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

23

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http://api.crossref.org/works/10.1016%2Fj.tet.2006.03.034

Identifiers

10.1016/J.TET.2006.03.034

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