PPT-Enantioselective

XH insertion reactions based on carbenoids Speaker Shaolong Zhang Supervisor David Zhigang Wang Date Jan 3 nd 2014 1 Outline Background Construction of CX bond via metal . brPage 2br 2 brPage 3br 3 brPage 4br 4 brPage 5br 5 of . olefin. Baihua. YE. 06/06/2011. Summary. 1. Introduction. 2. . Rhodium-. catalyzed. . i. ntermolecular. . hydroamination. 2.1. Rh-. catalyzed. . hydroamination. of . ethylene. 2.2. . Rh-. catalyzed. Aldehyde C-H Activation. Hua Wu (. Jieping. Zhu’s Lab). Laboratory. of . Synthesis. and Natural . Products. (. LSPN. ). Ecole Polytechnique Fédérale . de . Lausanne (. EPFL. ). 1. Group Seminar. SONEAS Swiss - based XiMo AG focuses on the development and application of proprietary metathesis catalysts for use in the specialty chemical, agro chemical, renewables, pharmaceutical, polymers an H imines s. Wangqing Kong . Zhu’s group meeting. 2. 3. th. , Feb, 2017. Outline. 1. I. ntroduction. 2. . Methods for C. ontrol of . Asymmetr. y . in Radical Chemistry. . (1) . Chiral Lewis Acid Chelation. Written by world-renowned and best-selling experts, Nobel Laureate E. J. Corey and Laszlo Kurti, Enantioselective Chemical Synthesis offers an authoritative and comprehensive overview of the field\'s progress the processes and tools for key formations future development for complex, stereocontrolled (enantiomeric or diastereoisomeric) molecules and valuable examples of multi-step syntheses. Utilizing a color-coded scheme to illustrate chemical transformations, Enantioselective Chemical Synthesis provides clear explanation and guidance through vital asymmetrical syntheses and insight into the next steps for the field. Researchers, professionals, and academics will benefit from this valuable, thorough, and unique resource.In Part I, the authors present clearly, comprehensively and concisely the most useful enantioselective processes available to synthetic chemists. Part II provides an extensive discussion of the most logical ways to apply these new enantioselective methods to the planning of syntheses of stereochemically complex molecules. This hitherto neglected area is essential for the advancement of enantioselective synthesis to a more rational and powerful level. Part III describes in detail many reaction sequences which have been used successfully for the construction of a wide variety of complex target molecules (+)-. Aberrarone. Erick . M. . Carreira. . Eidgenössiche. . Technische. . Hochschule. Zürich. . . J. Am. Chem. Soc. . 2022 . Publication . Date: August 19, . 2022. https://doi.org/10.1021/jacs.2c07150. Teerawat. . Songsichan. 1. st. June 2017. Laboratory of Synthesis and Natural Products (LSPN). Content. 1. Introduction. 2. Electrophilic Fluorination. 2.1 Metal-Catalyzed Fluorination Involving Enolates.