Dan weix cross electrophile coupling

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August undefined, 2024

WebThe Weix group is focused on the development of new reactions for organic synthesis, the development of new concepts in catalysis, and the study of reaction mechanisms. Our …

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Cross electrophile coupling is a type of cross-coupling reaction that occurs between two electrophiles often catalyzed by transition metal catalyst(s). Unlike conventional cross-coupling reactions of an electrophile with an organometallic reagent, the coupling partners in cross electrophile coupling reactions are both electrophiles. Generally, additional reductant to regenerate active catalyst is needed in this reaction. WebJan 13, 2024 · Matt then pursued a postdoctoral position with Professor Dan Weix at the University of Rochester before moving with Professor Weix to the University of Wisconsin – Madison. In the Weix Lab he contributed to cross-electrophile coupling methodology and discovered his fascination with nickel as a base metal suitable for scaleup, green … alertmedia mobile app

PUBLICATIONS – WEIX RESEARCH GROUP – UW–Madison

WebJul 9, 2024 · A tale of two esters: Abundant carboxylic acids can be converted into dialkyl and aryl alkyl ketones through a decarboxylative, non-symmetric coupling. The keys to this approach are the use of a nickel catalyst with an electron-poor bipyridine or terpyridine ligand, a THF/DMA mixed solvent system, and ZnCl 2 to enhance the reactivity of the … WebMay 13, 2014 · The purpose of this Synopsis is to introduce the variety of approaches known for the selective joining of two different electrophiles … WebA variety of cross-electrophile coupling reactions that have been developed in the Weix group, including aryl halides with alkyl halides, alkyl halides with acid chlorides, enones … alertmedia inc

Ni-Catalyzed Formal Cross-Electrophile Coupling of Alcohols …

Stoichiometric Reactions of Acylnickel (II) Complexes with ...

WebDec 17, 2024 · Despite their importance to medicine and materials science, the synthesis of biheteroaryls by cross-coupling remains challenging. We describe here a new, general approach to biheteroaryls: the Ni- and Pd-catalyzed multimetallic cross-Ullmann coupling of heteroaryl halides with triflates. An array of 5-membered, 6-membered, and fused … WebAug 5, 2024 · We report here the coupling reactions between vinyl/aryl and alkyl C–O electrophiles that can be derived from chemical feedstocks and naturally occurring functional groups. This method provides an efficient approach to the synthesis of a wide range of functionalized, and/or secondary alkyl substituted cycloa alertmedia integrationsWebDec 21, 2024 · Although alcohols are one of the largest pools of alkyl substrates, approaches to utilize them in cross-coupling and cross-electrophile coupling are limited. We report the use of 1° and 2° alcohols in cross-electrophile coupling with aryl and vinyl halides to form C(sp3)–C(sp2) bonds in a one-pot strategy utilizing a very fast (<1 min) … alertmedia provisioning

"WebNov 18, 2014 · Dan Weix. Department of Chemistry University of Rochester. Weix Group . Research Area: Inorganic Chemistry . The Power of Two: Multimetallic Approaches to Cross-Electrophile Coupling. Cross-electrophile coupling is the broadly-defined union of two different electrophiles through transition-metal catalysis under reducing conditions. … " - Dan weix cross electrophile coupling

Dan weix cross electrophile coupling

Asymmetric Induction in the Electrochemical Cross-Coupling of …

WebMay 15, 2014 · The purpose of this Synopsis is to introduce the variety of approaches known for the selective joining of two different electrophiles (R 1 -X and R 2 -X, Figure 1) … WebThese new ligands gave improved yields for challenging cross-couplings of pharmaceutically relevant substrates compared with those of those of previously published ligands. Keywords: alkyl-halides, allylic acetates, …

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WebDirect coupling of unactivated alcohols remains a challenge in current synthetic chemistry. We herein demonstrate a strategy building upon in situ halogenation/reductive coupling of alcohols with aryl halides to forge Csp2–Csp3 bonds. The combination of 2-chloro-3-ethylbenzo[d]oxazol-3-ium salt (CEBO) and TBAB as the mild bromination reagents … WebSep 4, 2024 · The C(sp3)–C(sp3) cross-coupling of alkyl halides with alkyl tosylates has been developed by employing a combination of nickel and nucleophilic cobalt catalysts in the presence of a manganese reductant. This method provides a straightforward route to a diverse set of not only secondary–primary but also primary–primary C(sp3)–C(sp3) …

WebA variety of cross-electrophile coupling reactions that have been developed in the Weix group, including aryl halides with alkyl halides, alkyl halides with acid chlorides, enones … WebFeb 21, 2024 · Main. Transition-metal-catalysed cross-coupling represents one of the most reliable approaches towards the formation of carbon–carbon (C–C) bonds in organic synthesis 6. These transformations ...

WebJun 20, 2024 · Alkyl chlorides are bench-stable chemical feedstocks that remain among the most underutilized electrophile classes in transition metal catalysis. Overcoming intrinsic limitations of C(sp3)–Cl bond activation, we report the development of a novel organosilane reagent that can participate in chlorine atom abstraction under mild photocatalytic … WebFeb 10, 2016 · he formation of Csp2−Csp3 bonds by cross-coupling has advanced rapidly in recent years,1 but remains less advanced than the synthesis of Csp 2−Csp bonds. One challenge for these cross-coupling reactions is the lower availability of alkyl coupling reagents compared to aryl coupling reagents.2 As a potential solution, alkanoic acids …

WebJul 21, 2024 · Despite their importance, the synthesis of alkylated heterocycles from the cross-coupling of Lewis basic nitrogen heteroaryl halides with alkyl halides remains a challenge. We report here a general solution to this challenge enabled by a new collection of ligands based around 2-pyridyl-N-cyanocarboxamidine and 2-pyridylcarboxamidine cores.

WebThe first nickel-catalyzed, magnesium-mediated reductive cross-coupling between benzyl chlorides and aryl chlorides or fluorides is reported. A variety of diarylmethanes can be prepared in good to excellent yields in a one-pot manner using easy-to-access mixed PPh3/NHC Ni(II) complexes of Ni(PPh3)(NHC)Br2 (NHC = 1,3-bis(2,6 … alertmedia proWebMethods and Mechanisms for Cross-Electrophile Coupling of Csp 2 Halides with Alkyl Electrophiles. DJ Weix. Accounts of Chemical Research 48 (6), 1767-1775. , 2015. 646. 2015. Mechanism and selectivity in nickel-catalyzed cross-electrophile coupling of aryl halides with alkyl halides. S Biswas, DJ Weix. Journal of the American Chemical Society ... alertmaster audio alarm transmitterWeb17. Everson, D. A.; Weix, D. J. Cross-electrophile coupling: principles of reactivity and selectivity. J. Org. Chem. 2014, 79, 4793-8. 16. Everson, D. A.; Buonomo, J. A.; Weix, D. … Joined In: 2024 Ph.D. 2024 (Chemistry), Shanghai Institute of Organic Chemistry … alertmedia sign in