Results 1 to 10 of about 374,817 (289)

Advances in Cross-Coupling Reactions [PDF]

open access: yesMolecules, 2020
Cross-coupling reactions stand among the most important reactions in chemistry [...]
José Pérez Sestelo, Luis A. Sarandeses
doaj   +3 more sources

Synthesis of fluoroalkenes and fluoroenynes via cross-coupling reactions using novel multihalogenated vinyl ethers [PDF]

open access: yesBeilstein Journal of Organic Chemistry
In this study, we develop the synthesis methods of fluoroalkenes and fluoroenynes via Suzuki–Miyaura and Sonogashira cross-coupling reactions using novel multihalogenated fluorovinyl ethers, which are easily prepared from the reaction between phenols and
Yukiko Karuo   +5 more
doaj   +2 more sources

Vinyl Esters and Vinyl Sulfonates as Green Alternatives to Vinyl Bromide for the Synthesis of Monosubstituted Alkenes via Transition-Metal-Catalyzed Reactions

open access: yesChemistry, 2023
This review summarizes the applications of vinyl sulfonate and vinyl acetate as green alternatives for vinyl bromide in cross-coupling reactions. In the first part, the preparation of vinyl sulfonates and their cross-coupling reactions are briefly ...
Tomáš Tobrman
doaj   +1 more source

Palladium-Catalyzed Cross-Coupling Reaction of Bis(cyclopentadienyl)diaryltitaniums with Terminal Alkynes

open access: yesReactions, 2023
Organotitanium compounds find application in diverse reactions, including carbon–carbon bond formation and oxidation. While titanium (IV) compounds have been used in various applications, the potential of bis(cyclopentadienyl)diaryltitanium in cross ...
Yuki Murata   +3 more
doaj   +1 more source

Microwave-assisted synthesis of a MK2 inhibitor by Suzuki-Miyaura coupling for study in Werner syndrome cells [PDF]

open access: yes, 2015
Microwave-assisted Suzuki-Miyaura cross-coupling reactions have been employed towards the synthesis of three different MAPKAPK2 (MK2) inhibitors to study accelerated aging in Werner syndrome (WS) cells, including the cross-coupling of a 2-chloroquinoline
Bagley, Mark C   +5 more
core   +7 more sources

Cross-coupling Reactions of Monosubstituted Tetrazines [PDF]

open access: yesOrganic Letters, 2021
A fast and mild method for the Pd-catalyzed cross-coupling reaction of monosubstituted 3-bromo-1,2,4,5-tetrazine is presented. Investigation of silver-based additives revealed that Ag2CO3 is the optimal mediator, enabling the process without the need for strong bases or high temperatures.
Hoff, Lukas V   +4 more
openaire   +3 more sources

Cross sections for pentaquark baryon production from protons in reactions induced by hadrons and photons [PDF]

open access: yes, 2003
Using hadronic Lagrangians that include the interaction of pentaquark $\Theta^+$ baryon with $K$ and $N$, we evaluate the cross sections for its production from meson-proton, proton-proton, and photon-proton reactions near threshold.
C. H. Li   +7 more
core   +2 more sources

Impact of Cross-Coupling Reactions in Drug Discovery and Development

open access: yesMolecules, 2020
Cross-coupling reactions have played a critical role enabling the rapid expansion of structure–activity relationships (SAR) during the drug discovery phase to identify a clinical candidate and facilitate subsequent drug development processes.
Melissa J. Buskes, Maria-Jesus Blanco
doaj   +1 more source

Validity of the linear coupling approximation in heavy-ion fusion reactions at sub barrier energies [PDF]

open access: yes, 1996
The role of higher order coupling of surface vibrations to the relative motion in heavy-ion fusion reactions at near-barrier energies is investigated.
Dasgupta, M.   +4 more
core   +3 more sources

Recent Applications of Pd-Catalyzed Suzuki–Miyaura and Buchwald–Hartwig Couplings in Pharmaceutical Process Chemistry

open access: yesOrganics, 2022
Cross-coupling reactions have changed the way complex molecules are synthesized. In particular, Suzuki–Miyaura and Buchwald–Hartwig amination reactions have given opportunities to elegantly make pharmaceutical ingredients.
Balaram S. Takale   +2 more
doaj   +1 more source

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