Convergent Approaches for the Synthesis of the Antitumoral Peptide, Kahalalide F. Study of Orthogonal Protecting Groups-Reference-Cited by-同舟云学术

Convergent Approaches for the Synthesis of the Antitumoral Peptide, Kahalalide F. Study of Orthogonal Protecting Groups

Published:2006-08-24 Issue:19 Volume:71 Page:7196-7204
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gracia Carolina¹,Isidro-Llobet Albert¹,Cruz Luis J.¹,Acosta Gerardo A.¹,Álvarez Mercedes¹,Cuevas Carmen¹,Giralt Ernest¹,Albericio Fernando¹

Affiliation:

1. Institute for Research in Biomedicine, Barcelona Science Park, University of Barcelona, 08028-Barcelona, Spain, Laboratory of Organic Chemistry, Faculty of Pharmacy, University of Barcelona, 08028-Barcelona, Spain, PharmaMar S.A.U., 28770-Colmenar Viejo (Madrid), Spain, and Department of Organic Chemistry, University of Barcelona, Martí i Franqués 1, 08028-Barcelona, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo060976f

Reference39 articles.

1. Kahalalide F: a bioactive depsipeptide from the sacoglossan mollusk Elysia rufescens and the green alga Bryopsis sp

2. Kahalalide F Induces Necrosis-Like Cell Death that Involves Depletion of ErbB3 and Inhibition of Akt Signaling

3. New Marine Derived Anticancer Therapeutics ─ A Journey from the Sea to Clinical Trials

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