Publications of Benjamin List

Rader, C.; List, B. Catalytic Antibodies as Magic Bullets. Chemistry – A European Journal 2000, 6, 2091–2095.

Karlstrom, A.; Zhong, G.; Rader, C.; Larsen, N. A.; Heine, A.; Fuller, R.; List, B.; Tanaka, F.; Wilson, I. A.; Barbas III, C. F.; Lerner, R. A. Using Antibody Catalysis to Study the Outcome of Multiple Evolutionary Trials of a Chemical Taskk. Proceedings of the National Academy of Sciences of the United States of America 2000, 97, 3878–3883.

List, B.; Lerner, R. A.; Barbas III, C. F. Proline-Catalyzed Direct Asymmetric Aldol Reactions. Journal of the American Chemical Society 2000, 122, 2395–2396.

List, B.; Shabat, D.; Zhong, G.; Turner, J. M.; Li, A.; Bui, T.; Anderson, J.; Lerner, R. A.; Barbas III, C. F. A Catalytic Enantioselective Route to Hydroxy-Substituted Quaternary Carbon Centers: Resolution of Tertiary Aldols with a Catalytic Antibody. Journal of the American Chemical Society 1999, 121, 7283–7291.

List, B.; Lerner, R. A.; Barbas III, C. F. Enantioselective Aldol Cyclodehydrations Catalyzed by Antibody 38C2. Organic Letters 1999, 1, 59–62.

Shabat, D.; Rader, C.; List, B.; Lerner, R. A.; Barbas, C. F. Multiple Event Activation of a Generic Prodrug Trigger by Antibody Catalysis. Proceedings of the National Academy of Sciences of the United States of America 1999, 96, 6925–6930.

Shabat, D.; List, B.; Lerner, R. A.; Barbas III, C. F. A Short Enantioselective Synthesis of 1-Deoxy-L-Xylulose by Antibody Catalysis. Tetrahedron Letters 1999, 40, 1437–1440.

List, B.; Barbas III, C. F.; Lerner, R. A. Aldol Sensors for the Rapid Generation of Tunable Fluorescence by Antibody Catalysis. Proceedings of the National Academy of Sciences of the United States of America 1998, 95, 15351–15355.

Zhong, G.; Shabat , D.; List, B.; Anderson, J.; Sinha, S. C.; Lerner, R. A.; Barbas, C. F. Catalytic Enantioselective Retro‐Aldol Reactions: Kinetic Resolution of β‐Hydroxyketones with Aldolase Antibodies. Angewandte Chemie International Edition 1998, 37, 2481–2484.

List, B.; Shabat, D.; Barbas III, C. F.; Lerner, R. A. Enantioselective Total Synthesis of Some Brevicomins Using Aldolase Antibody 38C2. Chemistry – A European Journal 1998, 4, 881–885.

Barbas III, C. F.; List, B. Alchemy, Enzymes, and the Blind-Watchmaker. Nature Biotechnology 1998, 16, 423–424.

Hoffmann, T.; Zhong, G.; List, B.; Shabat, D.; Anderson, J.; Gramatikova , S.; Lerner, R. A.; Barbas III, C. F. Aldolase Antibodies of Remarkable Scope. Journal of the American Chemical Society 1998, 120, 2768–2779.

Barbas III, C. F.; Heine, A.; Zhong, G.; Hoffmann, T.; Gramatikova, S.; Björnestedt, R.; List, B.; Anderson, J.; Stura, E. A.; Wilson, I. A.; Lerner, R. A. Immune Versus Natural Selection: Antibody Aldolases with Enzymic Rates But Broader Scope. Science 1997, 278, 2085–2092.

Mulzer, J.; List, B.; Bats, J. W. Stereocontrolled Synthesis of a Nonracemic Vitamin B₁₂ A−B-Semicorrin. Journal of the American Chemical Society 1997, 119, 5512–5518.

Mulzer, J.; Bats, J. W.; List, B.; Opatz, T.; Trauner, D. The Phenanthrenone Approach to Opium Alkaloids: Formal Total Synthesis of Morphine by Sigmatropic Rearrangement. Synlett 1997, 1997, 441–444.

Mulzer, J.; Martin, H. J.; List, B. One-Pot Three Component Synthesis of α, β-Unsaturated Ketones. Tetrahedron Letters 1996, 37, 9177–9178.

Mulzer, J.; List, B. [2,3]-Wittig Rearrangements of (Trimethylsilyl)Methyl Allyl Ethers. Tetrahedron Letters 1996, 37, 2403–2404.

Mulzer, J.; List, B. Highly Stereoselective Synthesis of Tetrasubstituted Alkenes Via [2,3]-Wittig Rearrangement. Tetrahedron Letters 1994, 35, 9021–9024.

Asymmetric Organocatalysis 1: Lewis Base and Acid Catalysts; List, B., Ed.; Georg Thieme Verlag KG: Stuttgart, 2012.

Čorić, I.; Vellalath, S.; Müller, S.; Cheng, X.; List, B. Developing Catalytic Asymmetric Acetalizations; Gooßen, L. J., Ed.; Gooßen, L. J., Series ed.; Topics in Organometallic Chemistry, Vol. 44: Inventing Reactions; Springer Verlag: Berlin Heidelberg, 2013; Vol. 44, pp 165–193.