Stereoselective Synthesis of the C9–C19 Fragment of Peloruside A-Reference-Cited by-同舟云学术

Stereoselective Synthesis of the C9–C19 Fragment of Peloruside A

Published:2016-06-03 Issue:12 Volume:18 Page:3018-3021
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Kennington Stuart C. D.¹,Romo Juan M.¹,Romea Pedro¹,Urpí Fèlix¹

Affiliation:

1. Secció de Química Orgànica, Departament de Química Inorgànica i Orgànica and Institut de Biomedicina de la Universitat de Barcelona (IBUB), Universitat de Barcelona, Carrer Martí i Franqués 1-11, 08028 Barcelona, Catalonia, Spain

Funder

Ministerio de Economía y Competitividad

Generalitat de Catalunya

European Regional Development Fund

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.6b01428

Reference53 articles.

1. Peloruside A: A Potent Cytotoxic Macrolide Isolated from the New Zealand Marine Sponge Mycale sp.

2. A Chemoenzymatic Approach to the Stereocontrolled Synthesis of the C1-C11 fragment of (+)-Peloruside A

3. Peloruside A Does Not Bind to the Taxoid Site on β-Tubulin and Retains Its Activity in Multidrug-Resistant Cell Lines

4. Peloruside A enhances apoptosis in H-ras-transformed cells and is cytotoxic to proliferating T cells

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