A highly step-economical synthesis of dictyostatin. - sprookjes - yvandenbroek - TriplyDB

A highly step-economical synthesis of dictyostatin.

A highly step-economical synthesis of dictyostatin.

http://www.wikidata.org/entity/Q37267008

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Marine Invertebrate Metabolites with Anticancer Activities: Solutions to the "Supply Problem"Synthesis of (+)-discodermolide by catalytic stereoselective borylation reactions.Conformation-activity relationships of polyketide natural products.Enantioselective Hydroformylation of 1-Alkenes with Commercial Ph-BPE Ligand A "methyl extension" strategy for polyketide natural product linker site validation and its application to dictyostatin.Beyond the Roche ester: a new approach to polypropionate stereotriad synthesis Recent progress with microtubule stabilizers: new compounds, binding modes and cellular activities.Stereoselective Synthesis and Retentive Trapping of α-Chiral Secondary Alkyllithiums Leading to Stereodefined α,β-Dimethyl Carboxylic Esters.Evolution of an Efficient and Scalable Nine-Step (Longest Linear Sequence) Synthesis of Zincophorin Methyl Ester.Stereocontrolled Synthesis of Polypropionate Fragments based on a Building Block Assembly Strategy using Lithiation-Borylation Methodologies.Design and 22-step synthesis of highly potent D-ring modified and linker-equipped analogs of spongistatin 1

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P2860

A highly step-economical synthesis of dictyostatin.

http://www.wikidata.org/entity/Q37267008

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 10 May 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

A highly step-economical synthesis of dictyostatin.

@en

A highly step-economical synthesis of dictyostatin.

@nl

type

label

A highly step-economical synthesis of dictyostatin.

@en

A highly step-economical synthesis of dictyostatin.

@nl

prefLabel

A highly step-economical synthesis of dictyostatin.

@en

A highly step-economical synthesis of dictyostatin.

@nl

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Angewandte Chemie International Edition

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A highly step-economical synthesis of dictyostatin.

@en

P2093

Cyril Bucher

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

James L Leighton

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

Stephen Ho

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

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Reaction of the acetals with TESOTf-base combination; speculation of the intermediates and efficient mixed acetal formation

Direct and highly regioselective and enantioselective allylation of β-diketones

An "aprotic" Tamao oxidation/syn-selective tautomerization reaction for the efficient synthesis of the C1-C9 fragment of fludelone

The bound conformation of microtubule-stabilizing agents: NMR insights into the bioactive 3D structure of discodermolide and dictyostatin.

Total synthesis of a library of designed hybrids of the microtubule-stabilising anticancer agents taxol, discodermolide and dictyostatin.

Dictyostatin flexibility bridges conformations in solution and in the β-tubulin taxane binding site.

Streamlined syntheses of (-)-dictyostatin, 16-desmethyl-25,26-dihydrodictyostatin, and 6-epi-16-desmethyl-25,26-dihydrodictyostatin

Toward a more step-economical and scalable synthesis of spongistatin 1 to facilitate cancer drug development efforts

Complex fragment coupling by crotylation: A powerful tool for polyketide natural product synthesis

A new and more powerfully activating diamine for practical and scalable enantioselective aldehyde crotylsilylation reactions.

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6757-6761

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scholarly article

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10.1002/ANIE.201302565

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26

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52

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2013-05-10T00:00:00Z

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23666786

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3812691

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