Absolute stereostructures of inoterpenes A–F from sclerotia of Inonotus obliquus (Q78296189)

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

13 December 2019

title

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

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

13 December 2019

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

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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

inferred from

reverse claim

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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(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

inferred from

reverse claim

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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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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Seikou Nakamura

1

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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

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

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

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

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

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

13 December 2019

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

13 December 2019

volume

65

1 reference

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

13 December 2019

issue

12

1 reference

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

13 December 2019

page(s)

2443-2450

1 reference

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

13 December 2019

Identifiers

1 reference

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