Revised structure of podolactone C, the antileukemic component of Podocarpus milanjianus Rendle (Q104952870)

http://api.crossref.org/works/10.1021%2Fjo00179a040

main subject

Podocarpus milanjianus

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Podocarpus latifolius

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(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2S)-1,2-dihydroxypropan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.02,4.04,9.012,14.015,18]octadec-8-ene-7,16-dione

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1 reference

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(1S,2R,4S,5R,10S,14R,17R)-5-[(2S)-2-hydroxy-1-[(R)-methylsulfinyl]propan-2-yl]-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione

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Nagilactone F,8-epoxy-

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(1S,2R,4S,5R,10S,11S,13R,14R,15R,18R)-5-[(2R)-1,2-dihydroxypropan-2-yl]-14-hydroxy-10,15-dimethyl-3,6,12,17-tetraoxahexacyclo[8.7.1.02,4.04,9.011,13.015,18]octadec-8-ene-7,16-dione

1 reference

1 reference

5-(2-Hydroxy-1-methylsulfinylpropan-2-yl)-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione

1 reference

1 reference

(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2S)-2-hydroxy-1-methylsulfinylpropan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.02,4.04,9.012,14.015,18]octadec-8-ene-7,16-dione

1 reference

1 reference

8,15-Dihydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione

1 reference

5-(1,2-Dihydroxypropan-2-yl)-14-hydroxy-10,15-dimethyl-3,6,12,17-tetraoxahexacyclo[8.7.1.02,4.04,9.011,13.015,18]octadec-8-ene-7,16-dione

1 reference

5-(1,2-Dihydroxypropan-2-yl)-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.02,4.04,9.012,14.015,18]octadec-8-ene-7,16-dione

1 reference

Podocarpus philippinensis

Podocarpus neriifolius

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1 reference

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Podocarpus polystachyus

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Podocarpus macrophyllus

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John M. Cassady

1

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http://api.crossref.org/works/10.1021%2Fjo00179a040

Teresa K. Lightner

2

1 reference

http://api.crossref.org/works/10.1021%2Fjo00179a040

Thomas G. McCloud

3

1 reference

http://api.crossref.org/works/10.1021%2Fjo00179a040

Johnny A. Hembree

4

1 reference

http://api.crossref.org/works/10.1021%2Fjo00179a040

Stephen R. Byrn

5

1 reference

http://api.crossref.org/works/10.1021%2Fjo00179a040

Chingjer Chang

6

1 reference

http://api.crossref.org/works/10.1021%2Fjo00179a040

publication date

March 1984

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16 September 2022

16 September 2022

4

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based on heuristic

inferred from page(s)

published in

Journal of Organic Chemistry

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http://api.crossref.org/works/10.1021%2Fjo00179a040

volume

49

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http://api.crossref.org/works/10.1021%2Fjo00179a040

issue

5

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http://api.crossref.org/works/10.1021%2Fjo00179a040

page(s)

942-945

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