Convergent Synthesis of PI3K Inhibitor GDC-0908 Featuring Palladium-Catalyzed Direct C–H Arylation toward Dihydrobenzothienooxepines

Author:

Zhang Haiming1ORCID,Li Beryl X.1,Wong Brian1,Stumpf Andreas1,Sowell C. Gregory1,Gosselin Francis1ORCID

Affiliation:

1. Department of Small Molecule Process Chemistry, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Reference25 articles.

1. Targeting the phosphoinositide 3-kinase pathway in cancer

2. The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism

3. Oncogenic PI3K deregulates transcription and translation

4. The phosphatidylinositol 3-Kinase–AKT pathway in human cancer

5. Blaquiere, N.; Do, S.; Dudley, D.; Folkes, A. J.; Goldsmith, R. A.; Heald, R.; Heffron, T.; Kolesnikov, A.; Ndubaku, C.; Olivero, A. G.; Price, S.; Staben, S.; Wei, B. Benzoxepin derivatives as PI3K inhibitor and their preparation and use in the treatment of cancer. PCT Int. Appl. 2011036284.

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