Results 101 to 110 of about 395,120 (176)
New Concepts for Organocatalysis
Organocatalysis, catalysis with low-molecular weight catalysts in which a metal is not part of the catalytic principle or the reaction substrate, can be as efficient and selective as metal- or biocatalysis.
List, B., B. List, Pan, S., S. C. Pan
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Recent Progress in the Asymmetric Organocatalysis
AbstractFor Abstract see ChemInform Abstract in Full Text.
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Asymmetric organocatalysis on a technical scale: current status and future challenges
Gröger H. Asymmetric organocatalysis on a technical scale: current status and future challenges. In: Reetz MT, List B, Jaroch S, Weinmann H, Schering Stiftung, eds. Organocatalysis. Ernst Schering Foundation Symposium Proceedings, 2007-2.
Reetz, M.T. +6 more
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AVANÇOS RECENTES NA HIDROAMINAÇÃO DE COMPOSTOS INSATURADOS
This review presents thermodynamics and kinetics aspects of the hydroamination reaction, recent advancements on this field for non-activated alkenes, alkynes and allenes, employing transition metal catalysis or organocatalysis, including activation by ...
Luiz F. T. Novaes, Julio C. Pastre
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Among the current huge development activities in C-H functionalization, asymmetric oxidative C(sp(3))-H bond coupling strategies have remained underrepresented. Beyond the initial examples using chiral metal complexes, the use of organocatalysis provides
Stockerl, Sebastian +1 more
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Asymmetric Counteranion-Directed Lewis Acid Organocatalysis.
This work describes studies on asymmetric counteranion-directed Lewis acid organocatalysis. In the first part, the development of a catalytic asymmetric Hosomi–Sakurai reaction using BINOL-derived disulfonimides is described. Good to excellent yields and
van Gemmeren, M.
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Searching for untrodden paths in organocatalysis territory
In spite of the tremendous growth experienced by the field of asymmetric organocatalysis in the last decade, it is important to realize that we are still far away from having explored all of the possible pathways in organocatalysis ‘territory'; the ...
Xavier Companyó +12 more
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Synthesis of the Southern Tripeptide (C1–N12) of Sanglifehrins Using Asymmetric Organocatalysis
The tripeptide southern region of the novel cyclophilin binding natural product macrolides, namely sanglifehrins, is synthesized involving asymmetric organocatalysis as chirality-inducing step.
Radhika, Laghuvarapu +1 more
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Asymmetric Organocatalysis: The Emerging Utility of α,β-Unsaturated Acylammonium Salts. [PDF]
Vellalath S, Romo D.
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Enantiopurity-Dependent Peptide Coacervates and Asymmetric Organocatalysis. [PDF]
Vetrano A +21 more
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