Nineteen-Step Total Synthesis of (+)-Phorbol

Por Kawamura, Shuhei, Chu, Hang, Felding, Jakob, Baran, Phil S.
Publicado no Nature (2016)

Divergent synthesis of Thapsigargin analogs

Por Chu, Hang, Dünstl, Georg, Felding, Jakob, Baran, Phil S.
Publicado no Bioorg Med Chem Lett (2018)

Scalable Synthesis of (−)-Thapsigargin

Por Chu, Hang, Smith, Joel M., Felding, Jakob, Baran, Phil S.
Publicado no ACS Cent Sci (2016)

Development of a Concise Synthesis of Ouabagenin and Hydroxylated Corticosteroid Analogues

Por Renata, Hans, Zhou, Qianghui, Dünstl, Georg, Felding, Jakob, Merchant, Rohan R., Yeh, Chien-Hung, Baran, Phil S.
Publicado no J Am Chem Soc (2015)

Divergent Synthesis of Pyrone Diterpenes via Radical Cross Coupling

Por Merchant, Rohan R., Oberg, Kevin M., Lin, Yutong, Novak, Alexander J. E., Felding, Jakob, Baran, Phil S.
Publicado no J Am Chem Soc (2018)

C—H Oxidation of Ingenanes Enables Potent and Selective Protein Kinase C Isoform Activation

Por Jin, Yehua, Yeh, Chien‐Hung, Kuttruff, Christian A., Jørgensen, Lars, Dünstl, Georg, Felding, Jakob, Natarajan, Swaminathan R., Baran, Phil S.
Publicado no Angew Chem Int Ed Engl (2015)

Chemical Proteomics Identifies SLC25A20 as a Functional Target of the Ingenol Class of Actinic Keratosis Drugs

Por Parker, Christopher G., Kuttruff, Christian A., Galmozzi, Andrea, Jørgensen, Lars, Yeh, Chien-Hung, Hermanson, Daniel J., Wang, Yujia, Artola, Marta, McKerrall, Steven J., Josyln, Christopher M., Nørremark, Bjarne, Dünstl, Georg, Felding, Jakob, Saez, Enrique, Baran, Phil S., Cravatt, Benjamin F.
Publicado no ACS Cent Sci (2017)