Total synthesis of eudesmane terpenes by site-selective C-H oxidations. (Q46013534)

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scientific article published on 13 May 2009

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English	Total synthesis of eudesmane terpenes by site-selective C-H oxidations.	scientific article published on 13 May 2009

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19440196

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18 December 2017

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http://europepmc.org/abstract/MED/19440196

title

Total synthesis of eudesmane terpenes by site-selective C-H oxidations. (English)

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19440196

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18 December 2017

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Ke Chen

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1

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Europe PubMed Central

PubMed publication ID

19440196

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18 December 2017

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http://europepmc.org/abstract/MED/19440196

Phil S Baran

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2

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Europe PubMed Central

PubMed publication ID

19440196

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18 December 2017

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http://europepmc.org/abstract/MED/19440196

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English

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publication date

13 May 2009

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PubMed publication ID

19440196

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18 December 2017

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http://europepmc.org/abstract/MED/19440196

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Nature

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PubMed publication ID

19440196

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18 December 2017

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http://europepmc.org/abstract/MED/19440196

volume

459

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Europe PubMed Central

PubMed publication ID

19440196

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18 December 2017

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http://europepmc.org/abstract/MED/19440196

issue

7248

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Europe PubMed Central

PubMed publication ID

19440196

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18 December 2017

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http://europepmc.org/abstract/MED/19440196

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824-828

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PubMed publication ID

19440196

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cites work

Eudesmane sesquiterpenoids from the Asteraceae family

1 reference

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https://pubmed.ncbi.nlm.nih.gov/19440196

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12 December 2020

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Oxaziridine-mediated catalytic hydroxylation of unactivated 3 degrees C-H bonds using hydrogen peroxide

1 reference

stated in

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https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late-stage intermolecular CH activation for lead diversification: a highly chemoselective oxyfunctionalization of the C-9 position of potent bryostatin analogues

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Catalytic direct asymmetric Michael reactions: taming naked aldehyde donors

1 reference

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retrieved

12 December 2020

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A case study in biomimetic total synthesis: polyolefin carbocyclizations to terpenes and steroids

1 reference

stated in

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reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

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1,3-Diol synthesis via controlled, radical-mediated C-H functionalization

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diphenylprolinol methyl ether: a highly enantioselective catalyst for Michael addition of aldehydes to simple enones

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

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Dioxygen activation at mononuclear nonheme iron active sites: enzymes, models, and intermediates

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

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The isoprene rule and the biogenesis of terpenic compounds

1 reference

stated in

PubMed

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https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

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Modern synthetic efforts toward biologically active terpenes

1 reference

stated in

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12 December 2020

based on heuristic

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Catalytic oxidations of steroid substrates by artificial cytochrome p-450 enzymes

1 reference

stated in

PubMed

reference URL

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retrieved

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Taxol biosynthesis: taxane 13 alpha-hydroxylase is a cytochrome P450-dependent monooxygenase

1 reference

stated in

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reference URL

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retrieved

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New sesquiterpene lactones from Laurus nobilis leaves as inhibitors of nitric oxide production

1 reference

stated in

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reference URL

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retrieved

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Catalytic C–H functionalization by metal carbenoid and nitrenoid insertion

1 reference

stated in

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reference URL

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retrieved

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A predictably selective aliphatic C-H oxidation reaction for complex molecule synthesis

1 reference

stated in

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reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

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Catalytic enantioselective approach to the eudesmane sesquiterpenoids: total synthesis of (+)-carissone

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New Chemical Constituents from the EndophyteStreptomyces Species LR4612 Cultivated onMaytenus hookeri

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

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Hydrocarbon oxidation vs C-C bond-forming approaches for efficient syntheses of oxygenated molecules

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pattern recognition in retrosynthetic analysis: snapshots in total synthesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19440196

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cyclization Enzymes in the Biosynthesis of Monoterpenes, Sesquiterpenes, and Diterpenes

1 reference

stated in

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reference URL

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retrieved

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1 reference

stated in

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retrieved

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1 reference

stated in

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reference URL

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Über die relative Geschwindigkeit der Chromosäureoxydation sekundärer, alicyclischer Alkohole. Vorläufige Mitteilung

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10.1038/NATURE08043

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Europe PubMed Central

PubMed publication ID

19440196

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/19440196

Dimensions Publication ID

1037692865

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PubMed publication ID

19440196

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19440196

retrieved

18 December 2017

reference URL

http://europepmc.org/abstract/MED/19440196

 

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