Home / Seminar & Event /Past Seminars / (333) Reversible Reservoirs for Radicals. A Powerful Strategy for the Construction of Carbon-Carbon Bonds
Home / Seminar & Event /Past Seminars / (333) Reversible Reservoirs for Radicals. A Powerful Strategy for the Construction of Carbon-Carbon Bonds
(333) Reversible Reservoirs for Radicals. A Powerful Strategy for the Construction of Carbon-Carbon Bonds
Seminar: (333) Reversible Reservoirs for Radicals. A Powerful Strategy for the Construction of Carbon-Carbon Bonds
Speaker: Prof. Samir Z. Zard, Director of Research, Laboratoire de Synthèse Organique, CNRS, & Professor at Ecole Polytechnique
Time: 2018-10-31 11:00 to 2018-10-31 12:00
Venue: Meeting room (406), Building 24
Organizer:

Health Science Platform


Biography: Prof. Samir Z. Zard currently holds the positions of “Director of Research” (Exceptional Class) in the C. N. R. S. and part-time Professor at Ecole Polytechnique. Professor Zard was born in 1955 in Ife, Nigeria. His training as a chemist started at the American University of Beirut (interrupted by the civil war in 1975), then at Imperial College, London, and finally at the Institut de Chimie des Substances Naturelles at Gif-sur-Yvette, France, where he received his doctorate under the supervision of Professor Sir Derek Barton in 1983. His main research concerns the study and development of new reactions and processes. He is the author of 357 scientific publications and 38 filed patents. In addition to a number of academic awards, he received in 2007 the Croix de Chevalier de la Légion d’Honneur.

 

Abstract: Radical reactions offer many of the properties desired by synthetic organic chemists, in terms of variety, mildness of conditions, and a selectivity that is often complementary to that of ionic chemistry, making many protection steps superfluous. There is however one major difficulty, which derives from the propensity of radicals to interact with themselves (dimerisation, disproportionation) with extremely fast rates that are close to diffusion. In order to overcome this complication, it is essential to keep the steady-state concentration of radical species very low. This can be accomplished for example by contriving a chain reaction where the propagating steps are themselves quite fast, as for example in the typical, and now extremely popular, stannane based processes. While various unimolecular cyclisation and fragmentation steps can be efficiently incorporated into the radical sequence, kinetically slower bimolecular transformations, and in particular intermolecular additions to un-activated alkenes, have proven more difficult to implement. In the case of stannanes, the relatively slow addition to the alkene has to compete with premature hydrogen atom abstraction from the organotin hydride, a step that is usually thousands of times faster.

      Over the years, we have shown that xanthates and related thiocarbonylthio derivatives allow the generation of radicals under conditions where the radicals possess a considerably increased effective lifetime even in a concentrated medium. Intermolecular additions to un-activated alkenes, as well as a variety of reputedly difficult radical transformations can now be easily accomplished. No metals, heavy or otherwise, are required, and the starting materials and reagents are cheap and readily available. Complex, densely functionalized structures can be constructed in a convergent, modular fashion. In the course of our study of the scope and limitations of this chemistry, we have uncovered a few surprising transformations. Recent results and some mechanistic aspects will be presented and discussed briefly.


(333) Reversible Reservoirs for Radicals. A Powerful Strategy for the Construction of Carbon-Carbon Bonds
Seminar: (333) Reversible Reservoirs for Radicals. A Powerful Strategy for the Construction of Carbon-Carbon Bonds
Speaker: Prof. Samir Z. Zard, Director of Research, Laboratoire de Synthèse Organique, CNRS, & Professor at Ecole Polytechnique
Time: 2018-10-31 11:00 to 2018-10-31 12:00
Venue: Meeting room (406), Building 24
Organizer:

Health Science Platform


Biography: Prof. Samir Z. Zard currently holds the positions of “Director of Research” (Exceptional Class) in the C. N. R. S. and part-time Professor at Ecole Polytechnique. Professor Zard was born in 1955 in Ife, Nigeria. His training as a chemist started at the American University of Beirut (interrupted by the civil war in 1975), then at Imperial College, London, and finally at the Institut de Chimie des Substances Naturelles at Gif-sur-Yvette, France, where he received his doctorate under the supervision of Professor Sir Derek Barton in 1983. His main research concerns the study and development of new reactions and processes. He is the author of 357 scientific publications and 38 filed patents. In addition to a number of academic awards, he received in 2007 the Croix de Chevalier de la Légion d’Honneur.

 

Abstract: Radical reactions offer many of the properties desired by synthetic organic chemists, in terms of variety, mildness of conditions, and a selectivity that is often complementary to that of ionic chemistry, making many protection steps superfluous. There is however one major difficulty, which derives from the propensity of radicals to interact with themselves (dimerisation, disproportionation) with extremely fast rates that are close to diffusion. In order to overcome this complication, it is essential to keep the steady-state concentration of radical species very low. This can be accomplished for example by contriving a chain reaction where the propagating steps are themselves quite fast, as for example in the typical, and now extremely popular, stannane based processes. While various unimolecular cyclisation and fragmentation steps can be efficiently incorporated into the radical sequence, kinetically slower bimolecular transformations, and in particular intermolecular additions to un-activated alkenes, have proven more difficult to implement. In the case of stannanes, the relatively slow addition to the alkene has to compete with premature hydrogen atom abstraction from the organotin hydride, a step that is usually thousands of times faster.

      Over the years, we have shown that xanthates and related thiocarbonylthio derivatives allow the generation of radicals under conditions where the radicals possess a considerably increased effective lifetime even in a concentrated medium. Intermolecular additions to un-activated alkenes, as well as a variety of reputedly difficult radical transformations can now be easily accomplished. No metals, heavy or otherwise, are required, and the starting materials and reagents are cheap and readily available. Complex, densely functionalized structures can be constructed in a convergent, modular fashion. In the course of our study of the scope and limitations of this chemistry, we have uncovered a few surprising transformations. Recent results and some mechanistic aspects will be presented and discussed briefly.