Lecture

Reactive Intermediates: Annulations and Additions

Graph Chat

Chat with Graph Search

Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.

DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.

In course

CH-707: Frontiers in Chemical Synthesis. Towards Sustainable Chemistry

This training will empowered the student with all the tools of modern chemistry, which will be highly useful for his potential career as a process or medicinal chemist in industry. ...

Description

This lecture covers the types of reactive intermediates, background, main innovations, and selected examples in annulations and formal 1,2-additions. It explores the use of homo enolate equivalents, acyl azoliums, and conjugated enolate equivalents in various reactions. The instructor discusses the reactivity overview and concludes with future research directions.

Instructors (2)

Xile Hu

Xile Hu was born in 1978 in Putian, southeastern China. He entered the Peking University in Beijing in 1996. Besides learning too little chemistry, his biggest regret in the college was not able to correct his southern accent in Mandarin. After graduated from PKU, he went to the United States and began his doctoral studies at the University of California, San Diego. In December 2004, he finished with a Ph.D. in chemistry and some fond memories of the beautiful city of San Diego. He then moved to the Los Angeles area and become a postdoctoral scholar at the California Institute of Technology. There he enjoyed numerous stimulating scientific (and other) discussions with friends and colleagues. He also made plenty of friends outside the campus and was a frequent in many local Chinese restaurants. In 2007, after two pleasant visits to Switzerland, he decided to move across the continent one more time and join the faculty of the École Polytechnique Fédérale de Lausanne (EPFL). He now directs the Laboratory of Inorganic Synthesis and Catalysis and is interested in developing chemistry for synthesis, energy and sustainability.

Jérôme Waser

Jérôme Waser biography and CV's are available on the following website: http://lcso.epfl.ch/waser

Official source

Related concepts (32)

Michael addition reaction

In organic chemistry, the Michael reaction or Michael 1,4 addition is a reaction between a Michael donor (an enolate or other nucleophile) and a Michael acceptor (usually an α,β-unsaturated carbonyl) to produce a Michael adduct by creating a carbon-carbon bond at the acceptor's β-carbon. It belongs to the larger class of conjugate additions and is widely used for the mild formation of carbon-carbon bonds.

Addition reaction

In organic chemistry, an addition reaction is an organic reaction where two or more molecules combine to form a larger one (the adduct). Addition reactions are limited to chemical compounds that have multiple bonds, such as molecules with carbon–carbon double bonds (alkenes), or with triple bonds (alkynes), and compounds that have rings, which are also considered points of unsaturation. Molecules containing carbon—hetero double bonds like carbonyl () groups, or imine () groups, can undergo addition, as they too have double-bond character.

Nucleophilic addition

In organic chemistry, a nucleophilic addition reaction is an addition reaction where a chemical compound with an electrophilic double or triple bond reacts with a nucleophile, such that the double or triple bond is broken. Nucleophilic additions differ from electrophilic additions in that the former reactions involve the group to which atoms are added accepting electron pairs, whereas the latter reactions involve the group donating electron pairs.

Reactive intermediate

In chemistry, a reactive intermediate or an intermediate is a short-lived, high-energy, highly reactive molecule. When generated in a chemical reaction, it will quickly convert into a more stable molecule. Only in exceptional cases can these compounds be isolated and stored, e.g. low temperatures, matrix isolation. When their existence is indicated, reactive intermediates can help explain how a chemical reaction takes place.

Free-radical addition

In organic chemistry, free-radical addition is an addition reaction which involves free radicals. The addition may occur between a radical and a non-radical, or between two radicals. The basic steps with examples of the free-radical addition (also known as radical chain mechanism) are: Initiation by a radical initiator: A radical is created from a non-radical precursor.

Related lectures (53)

Catalytic Asymmetric Reactions in Organic Chemistry

Explores catalytic asymmetric reactions in organic chemistry, covering Lewis and Brønsted acids activation, Aldol Reaction, Allylation, Ene Reactions, and more.

Asymmetric Reactions in Organic Chemistry

Delves into asymmetric reactions in organic chemistry, highlighting mechanisms, catalysts, and selectivity.

Catalytic Asymmetric Reactions in Organic Chemistry

Covers catalytic asymmetric reactions, including activation of electrophiles, use of iodine reagents, and various catalytic reactions in organic chemistry.

Catalytic Asymmetric Reactions in Organic Chemistry

Explores catalytic asymmetric reactions in organic chemistry, focusing on proline-catalyzed reactions and amination of aldehydes and ketones.

Synthesis Strategies: Tamiflu

Covers the synthesis strategies for the active ingredient of Tamiflu, focusing on retrosynthesis and regioselective openings.

Related concepts (32)

Michael addition reaction

Addition reaction

Nucleophilic addition

Reactive intermediate

Free-radical addition