Absolute stereostructures of inoterpenes A–F from sclerotia of Inonotus obliquus (Q78296189): Difference between revisions

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scientific article published on 25 January 2009

Language	Label	Description	Also known as
English	Absolute stereostructures of inoterpenes A–F from sclerotia of Inonotus obliquus	scientific article published on 25 January 2009

Statements

scholarly article

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

Absolute stereostructures of inoterpenes A–F from sclerotia of Inonotus obliquus (English)

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

Inonotus obliquus

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trametenolic acid

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6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylheptane-2,3-diol

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1 reference

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(3S,5R,10S,13R,14R,17R)-17-[(E,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

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1 reference

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3beta-Hydroxy-lanosta-8,24-dien-21-al

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1 reference

17-(1-hydroxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

1-(6-hydroxy-6-methylhept-4-en-2-yl)-3a,6,6,9a,11a-pentamethyl-1H,2H,3H,4H,5H,5aH,7H,8H,9H,10H,11H-cyclopenta[a]phenanthren-7-ol

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1 reference

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(3S,5R,10S,13R,14R,17R)-17-[(2R)-6-hydroperoxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

1 reference

17-(2-Hydroxy-1,5-dimethyl-hex-4-enyl)-4,4,10,13,14-pentamethyl-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene

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1 reference

2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylhept-5-ene-1,3-diol

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author name string

Seikou Nakamura

1

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

Junko Iwami

2

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

Hisashi Matsuda

3

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

Shuichi Mizuno

4

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

Masayuki Yoshikawa

5

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

publication date

25 January 2009

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

65

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10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

12

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

2443-2450

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

Identifiers

10.1016/J.TET.2009.01.076

1 reference

10.1016/J.TET.2009.01.076

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.tet.2009.01.076

13 December 2019

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