Publications of Benjamin List

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.

Mahlau, M.; List, B. Asymmetric Counteranion-Directed Catalysis (ACDC). In Asymmetric Synthesis II; Christmann, M., Bräse, S., Eds.; Christmann, M., Bräse, S., Series Eds.; Wiley-VCH Verlag GmbH: Weinheim, 2012; pp 79–85.

List, B.; Liao, S.-H.; Shirakawa, S.; Maruoka, K.; Gong, L. Z.; Xiao, W.-J. The Proline-Catalyzed Mannich Reaction and the Advent of Enamine Catalysis. In Organic Chemistry - Breakthroughs and Perspectives; Ding, K., Dai, L.-X., Eds.; Ding, K., Dai, L.-X., Series Eds.; Wiley-VCH Verlag & Co. KGaA: Weinheim, 2012; pp 367–384.

Kampen, D.; Reisinger, C. M.; List, B. Chiral Brønsted Acids for Asymmetric Organocatalysis; List, B., Ed.; List, B., Series ed.; Topics in Current Chemistry, Vol. 291: Asymmetric Organocatalysis; Springer Verlag: Berlin Heidelberg, 2010; Vol. 291, pp 395–456.

List, B. Enough Organocatalysis?; List, B., Ed.; List, B., Series ed.; Topics in Current Chemistry, Vol. 291: Asymmetric Organocatalysis; Springer Verlag: Berlin Heidelberg, 2010; Vol. 291, pp ix-x.