Stereochemistry in All Its Shapes and Forms: The 56th Bürgenstock Conference.

M. Lancaster, M. Roemelt, P. Ettenhuber, Y. Hu, M. W. Ribbe, F. Neese, U. Bergmann, S. DeBeer, Science 2011, 334, 974 - 977; 71 Z. Mathe, O. McCubbin Stepanic, S. Peredkov, S. DeBeer, Chem. Sci. 2021, 12, 7888 - 7901; 72 Y. Pang, N. Nöthling, M. Leutzsch, L. Kang, E. Bill, M. van Gastel, E. Reijerse, R. Goddard, L. Wagner, D. SantaLucia, S. DeBeer, F. Neese, J. Cornella, Science 2023, 380, 1043 - 1048. Rev. 1955, 55, 625 - 657; 13 G. S. Hammond, P. A. Leermakers, N. J. Turro, J. Am. Chem. Soc. 1961, 83, 2396 - 2397; 14 J. Saltiel, G. S. Hammond, J. Am. Chem. Soc. 1963, 85, 2515 - 2516; 15 T. Arai, H. Sakuragi, K. Tokumaru, Chem. Keywords: Bürgenstock Conference; Catalysis; Chemical Biology; Organic Chemistry; Stereochemistry EN Bürgenstock Conference Catalysis Chemical Biology Organic Chemistry Stereochemistry 1 7 7 09/20/23 20230925 NES 230925 Acknowledging the crucial role of stereochemistry in fields as diverse as total synthesis, synthetic methodology, spectroscopy, and the study of the origin of life, the 56th SCS Conference on Stereochemistry, better known as the BÃ1/4rgenstock Conference, brought together a diverse range of chemistry expertise in Brunnen, Switzerland. 83 F. Neese, W. G. Zumft, W. E. Antholine, P. M. H. Kroneck, J. Am. Chem. Soc. 1996, 118, 8692 - 8699; 84 F. Neese, PhD thesis, Universität Konstanz, 1997; 85 F. Neese, Wiley Interdiscip. [Extracted from the article]