Site-selective C–H alkylation of complex arenes by a two-step aryl thianthrenation-reductive alkylation sequence

B Lansbergen, P Granatino, T Ritter - Journal of the American …, 2021 - ACS Publications
Herein, we present an undirected para-selective two-step C–H alkylation of complex arenes
useful for late-stage functionalization. The combination of a site-selective C–H …

Direct arene C–H fluorination with 18F via organic photoredox catalysis

W Chen, Z Huang, NES Tay, B Giglio, M Wang… - Science, 2019 - science.org
Positron emission tomography (PET) plays key roles in drug discovery and development, as
well as medical imaging. However, there is a dearth of efficient and simple radiolabeling …

Mechanochemical Activation of Zinc and Application to Negishi Cross‐Coupling

Q Cao, JL Howard, E Wheatley… - Angewandte …, 2018 - Wiley Online Library
A form independent activation of zinc, concomitant generation of organozinc species and
engagement in a Negishi cross‐coupling reaction via mechanochemical methods is …

Wittig/B─H insertion reaction: A unique access to trisubstituted Z-alkenes

FK Guo, YL Lu, MY Huang, JM Yang, JL Guo… - Science …, 2023 - science.org
The Wittig reaction, which is one of the most effective methods for synthesizing alkenes from
carbonyl compounds, generally gives thermodynamically stable E-alkenes, and synthesis of …

Efficient Pd‐Catalyzed Direct Coupling of Aryl Chlorides with Alkyllithium Reagents

T Scherpf, H Steinert, A Großjohann… - Angewandte …, 2020 - Wiley Online Library
Organolithium compounds are amongst the most important organometallic reagents and
frequently used in difficult metallation reactions. However, their direct use in the formation of …

Reductive Cross‐Coupling of a Vinyl Thianthrenium Salt and Secondary Alkyl Iodides

B Lansbergen, S Tewari, I Tomczyk… - Angewandte Chemie …, 2023 - Wiley Online Library
We report the first reductive vinylation of alkyl iodides. The reaction uses a vinyl
thianthrenium salt, a palladium catalyst, and an alkyl zinc intermediate formed in situ to trap …

Ni-Catalyzed reductive Liebeskind–Srogl alkylation of heterocycles

Y Ma, J Cammarata, J Cornella - Journal of the American …, 2019 - ACS Publications
Herein we present a Ni-catalyzed alkylation of C–SMe with alkyl bromides for the decoration
of heterocyclic frameworks. The protocol, reminiscent to the Liebeskind–Srogl coupling …

Regiodivergent enantioselective C–H functionalization of Boc-1,3-oxazinanes for the synthesis of β2- and β3-amino acids

W Lin, KF Zhang, O Baudoin - Nature catalysis, 2019 - nature.com
Abstract β2-and β3-amino acids are important chiral building blocks for the design of new
pharmaceuticals and peptidomimetics. Here, we report a straightforward regio-and …

Conversion of aldehydes to branched or linear ketones via regiodivergent rhodium-catalyzed vinyl bromide reductive coupling–redox isomerization mediated by …

RA Swyka, WG Shuler, BJ Spinello… - Journal of the …, 2019 - ACS Publications
A regiodivergent catalytic method for direct conversion of aldehydes to branched or linear
alkyl ketones is described. Rhodium complexes modified by P t Bu2Me catalyze formate …

Samarium-based Grignard-type addition of organohalides to carbonyl compounds under catalysis of CuI

S Xiao, C Liu, B Song, L Wang, Y Qi… - Chemical Communications, 2021 - pubs.rsc.org
Grignard-type additions were readily achieved under the mediation of CuI (10 mol%) and
samarium (2 equiv.) by employing various organohalides, eg benzyl, aryl, heterocyclic and …