(Q104999048)

http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

1 reference

[13,16-Dihydroxy-5-(hydroxymethyl)-2,11,12-trimethyl-6-oxo-7,17-dioxapentacyclo[10.3.1.13,15.05,15.08,13]heptadec-1-en-10-yl] 2-methylbut-2-enoate

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[5-(Acetyloxymethyl)-13-hydroxy-2,11,12-trimethyl-6-oxo-7,17-dioxapentacyclo[10.3.1.13,15.05,15.08,13]heptadec-1-en-16-yl] 2-methylprop-2-enoate

1 reference

[(3R,5S,8S,11S,12S,13S,15R,16S)-5-(acetyloxymethyl)-13-hydroxy-2,11,12-trimethyl-6-oxo-7,17-dioxapentacyclo[10.3.1.13,15.05,15.08,13]heptadec-1-en-16-yl] (Z)-2-methylbut-2-enoate

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1 reference

1 reference

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[13-Hydroxy-5-(hydroxymethyl)-2,11,12-trimethyl-6-oxo-7,17-dioxapentacyclo[10.3.1.13,15.05,15.08,13]heptadec-1-en-16-yl] 2-(hydroxymethyl)prop-2-enoate

1 reference

(2S,3R,5S,8S,11S,12S,13S,15R)-2,13-dihydroxy-5-(hydroxymethyl)-2,11,12-trimethyl-7,17-dioxapentacyclo[10.3.1.13,15.05,15.08,13]heptadec-1(16)-en-6-one

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2,13-Dihydroxy-5-(hydroxymethyl)-2,11,12-trimethyl-7,17-dioxapentacyclo[10.3.1.13,15.05,15.08,13]heptadec-1(16)-en-6-one

1 reference

[5-(Acetyloxymethyl)-13-hydroxy-2,11,12-trimethyl-6-oxo-7,17-dioxapentacyclo[10.3.1.13,15.05,15.08,13]heptadec-1-en-16-yl] 2-methylbut-2-enoate

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Yu Zhao

1

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

Simon Parsons

2

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

Bruce A. Smart

3

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

Renxiang Tan

4

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

Zhongjian Jia

5

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

Handong Sun

6

1 reference

http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

David W.H. Rankin

7

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

publication date

April 1997

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16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

volume

53

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

issue

17

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http://api.crossref.org/works/10.1016%2Fs0040-4020%2897%2900276-7

page(s)

6195-6208

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Sesquiterpenes and other constituents fromLigularia veitchiana

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Eremophilanolides from the roots of Ligularia veitchiana

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New Eremophilane Type Lactones from the Roots of Ligularia veitchiana

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Novel Sesquiterpenes from Ligularia veitchiana

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https://api.crossref.org/works/10.1016%2FS0040-4020%2897%2900276-7

7 January 2021

New Sesquiterpenes from the Roots of Ligularia veitchiana

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https://api.crossref.org/works/10.1016%2FS0040-4020%2897%2900276-7

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Ligulaverin A, a structurally novel sesquiterpenoid-derived metabolite possibly formed via a biological Diels–Alder reaction

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7 January 2021

The structure of euryopsol, a furanoeremophilane from Euryops species

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7 January 2021

Development and use of quantum mechanical molecular models. 76. AM1: a new general purpose quantum mechanical molecular model

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7 January 2021

Plant antitumor agents. VI. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia

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Synthesis of taxol from baccatin III via an oxazoline intermediate

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Discodermolide, a cytotoxic marine agent that stabilizes microtubules more potently than taxol

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7 January 2021

(+)-Discodermolide binds to microtubules in stoichiometric ratio to tubulin dimers, blocks taxol binding and results in mitotic arrest

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7 January 2021