Asymmetric synthesis, stereochemistry and rearrangement reactions of naturally occurring 7'-hydroxylignano-9,9'-lactones.

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Synthesis of 3,4-dibenzyltetrahydrofuran lignans (9,9'-epoxylignanes).Asymmetric Synthesis of β-Substituted α-Methylenebutyro- lactones via TRIP-Catalyzed Allylation: Mechanistic Studies and Application to the Synthesis of (S)-(-)-Hydroxymatairesinol.

P2860

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P2860

Asymmetric synthesis, stereochemistry and rearrangement reactions of naturally occurring 7'-hydroxylignano-9,9'-lactones.

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2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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2005年學術文章

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name

Asymmetric synthesis, stereoch ...... -hydroxylignano-9,9'-lactones.

@en

Asymmetric synthesis, stereoch ...... -hydroxylignano-9,9'-lactones.

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type

Item

label

Asymmetric synthesis, stereoch ...... -hydroxylignano-9,9'-lactones.

@en

Asymmetric synthesis, stereoch ...... -hydroxylignano-9,9'-lactones.

@nl

prefLabel

Asymmetric synthesis, stereoch ...... -hydroxylignano-9,9'-lactones.

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Asymmetric synthesis, stereoch ...... -hydroxylignano-9,9'-lactones.

@nl

P1476

Asymmetric synthesis, stereoch ...... -hydroxylignano-9,9'-lactones.

@en

P2093

Barbara Raffaelli

http://www.w3.org/2001/XMLSchema#string

Kristiina Wähälä

http://www.w3.org/2001/XMLSchema#string

Tapio Hase

http://www.w3.org/2001/XMLSchema#string

P2860

Podophyllum‐ Lignane: Struktur und Absolutkonfiguration von Podorhizol‐β‐D‐glucosid ( = Lignan F)†. 19. Mitt. über mitosehemmende Naturstoffe [1]

Hydroxymatairesinol, a novel enterolactone precursor with antitumor properties from coniferous tree (Picea abies).

In vitro metabolism of plant lignans: new precursors of mammalian lignans enterolactone and enterodiol.

alpha,beta-Dibenzyl-gamma-butyrolactone lignan alcohols: total synthesis of (+/-)-7'-hydroxyenterolactone, (+/-)-7'-hydroxymatairesinol and (+/-)-8-hydroxyenterolactone.

Free-radical-mediated conjugate additions. Enantioselective synthesis of butyrolactone natural products: (-)-enterolactone, (-)-arctigenin, (-)-isoarctigenin, (-)-nephrosteranic acid, and (-)-roccellaric acid.

Liquid chromatographic-tandem mass spectrometric method for the plant lignan 7-hydroxymatairesinol and its potential metabolites in human plasma.

A new lariciresinol-type butyrolactone lignan derived from hydroxymatairesinol and its identification in spruce wood.

Substitution of HMPT by the cyclic urea DMPU as a cosolvent for highly reactive nucleophiles and bases

Radical Carboxyarylation Approach to Lignans. Total Synthesis of (−)-Arctigenin, (−)-Matairesinol, and Related Natural Products

P304

331-341

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P31

scholarly article

P356

10.1039/B513303C

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P478

http://www.w3.org/2001/XMLSchema#string

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2005-12-12T00:00:00Z

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P698

16391776

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Asymmetric synthesis, stereochemistry and rearrangement reactions of naturally occurring 7'-hydroxylignano-9,9'-lactones.

about

P2860

P2860

Asymmetric synthesis, stereochemistry and rearrangement reactions of naturally occurring 7'-hydroxylignano-9,9'-lactones.

description

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P1433

P1476

P2093

P2860

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P698

P356

P1433

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P2860

P304

P31

P356

P433

P478

P577

P698