The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

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Synthesis of (+)-bullatacin via the highly diastereoselective [3+2] annulation reaction of a racemic aldehyde and a nonracemic allylsilane Alteration of the bis-tetrahydrofuran core stereochemistries in asimicin can affect the cytotoxicity Acetogenins from Annonaceae.

P2860

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P2860

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

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http://www.wikidata.org/entity/Q56952573

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wetenschappelijk artikel

@nl

наукова стаття, опублікована в грудні 2004

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name

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

@en

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

@nl

type

Item

label

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

@en

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

@nl

prefLabel

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

@en

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

@nl

P1476

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

@en

P2093

Darren J. Dixon

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

Gillian L. Nattrass

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

Matthew M. McLachlan

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

P2860

Total synthesis of the cytotoxic threo, trans, threo, trans, threo annonaceous acetogenin asimin and its C-10 epimer: unambiguous confirmation of absolute stereochemistry.

Total Synthesis of the Nonadjacent Bis-Tetrahydrofuran Annonaceous Acetogenin Squamostatin-D.

Total Synthesis of the Cytotoxic Threo, Trans, Erythro, Cis, Threo Annonaceous Acetogenin Trilobin.

A modular synthesis of annonaceous acetogenins.

Total synthesis and structure confirmation of the annonaceous acetogenins 30(S)-hydroxybullatacin, uvarigrandin a, and 5(R)-uvarigrandin a (narumicin I?).

Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ligands.

Annonaceous acetogenins: recent progress.

Formal synthesis of uvaricin via palladium-mediated double cyclization.

Total Synthesis of Uvaricin.

Diastereoselective temporary silicon-tethered ring-closing-metathesis reactions with prochiral alcohols: a new approach to long-range asymmetric induction.

P304

580-584

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P31

scholarly article

P356

10.1002/ANIE.200462264

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P407

English

P433

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

P478

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

P50

Elena Díez

Steven V. Ley

P577

2004-12-13T00:00:00Z

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P698

15597387

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P921

catalysis

general chemistry

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

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P2860

P2860

The Total Synthesis of the Annonaceous Acetogenin 10-Hydroxyasimicin

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921