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About Phil S Baran | Baran Lab Phil S Baran Professor, Department of Chemistry Member, Skaggs Institute for Chemical Biology pbaran@scripps edu Fax: (858) 784-7375 Tel: (858) 784-7373 Full CV The Genius Dialogues on Audible
Our Research - Baran Lab Our Mission is simple: Education at the intersection of fundamental organic chemistry and translational science Aiming for the Ideal Synthesis In the 20th century the art and science of complex natural product total synthesis defined the frontiers of organic chemistry Throughout these decades fundamental insights into reactivity and selectivity principles were achieved by these numerous
Publications - Baran Lab Guo, Y ; Li, Y ; Chen, S ; Poll, O ; Wu, Y ; Prier, C K ; Xiao, K -J ; Baran, P S Scalable, Convergent Total Synthesis of (+)-Saxitoxin and Related Natural Products
Explore Electrochemistry | Baran Lab Horn, E J ; Rosen, B R ; Baran, P S Synthetic Organic Electrochemistry: An Enabling and Innately Sustainable Method, ACS Cent Sci , 2016, 2, 302-308 (Free Download)
Group Seminars | Baran Lab Barry Snider (Krawczuk, 2007) The Barton Family Tree (Barton, 2017) BCSJ 1986-1990 (Kanda, 2015) Bernhard Witkop (Maue, 2006) Beyond the Rule of 5 (Hayashi, 2021) Bimetallic Complex in Organic Synthesis (Qin, 2015) The Big Grabowski (Cernijenko, 2014) Biginelli and Related Reactions (DeMartino, 2003) Biocatalysis (Gulder, 2009) Bioisosteres v2 – Recent Trends and Tactics (Smith, 2020
Group Members | Baran Lab Stockholm University The Swedish Research Council Fund Stiftelsen Bengt Lundqvists minne Fellowship
Dissertations - Baran Lab 2024 Brendyn Smith – Unlocking the Total Synthesis of Dragocins A–C: Adventures With Unusual Marine Hybrid Metabolites 2023 Junchen Tang – A Scalable, Enantioselective Total Synthesis of Two Anticancer Marine-Derived Natural Products: Portimine A and B Cheng Bi – Enantioselective Total Synthesis of (+)-KB343 Dongmin Xu – Synthesis of P-Chiral Phosphines and Methylphosphonate
CV-PSB-February 2019[2] - Baran Lab Baran, P S ; Richter, J M Direct Coupling of Indoles with Carbonyl Compounds: Short, Enantioselective, Gram-Scale Synthetic Entry into the Hapalindole and Fischerindole Alkaloid Families, J Am Chem Soc 2004, 126, 7450 – 7451