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Computational Organic Chemistry: The Frontier for Understanding and Designing Bioorthogonal Cycloadditions. [PDF]
Top Curr Chem (Cham)Svatunek D.
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Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions
Chemical Reviews, 2008AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Mukund P Sibi
exaly +6 more sources
Theory of 1,3-Dipolar Cycloadditions: Distortion/Interaction and Frontier Molecular Orbital Models
Journal of the American Chemical Society, 2008Quantum chemical calculations of activation barriers and reaction energies for 1,3-dipolar cycloadditions by the high-accuracy CBS-QB3 method reveal previously unrecognized quantitative trends in activation barriers.
K N Houk
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Asymmetric 1,3-Dipolar Cycloadditions
Tetrahedron, 2007This review is intended to update the recent developments in asymmetric 1,3-dipolar cycloaddition reactions involving a variety of heteroylides (or ylide equivalents) and dipolarophiles, covering the literature from 2001 to 2006. Figure options Download
H. Pellissier
semanticscholar +4 more sources
Natural 1,3-Dipolar Cycloadditions.
Angewandte Chemie International Edition, 2015[3+2] in the wild: Biomimetic natural product syntheses and theoretical considerations have indicated that 1,3-dipolar cycloadditions take place in nature.
M. Baunach, C. Hertweck
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Recent Advances of Catalytic Asymmetric 1,3-Dipolar Cycloadditions
Chemical Reviews, 2015Takuya Hashimoto, Keiji Maruoka
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Journal of Organic Chemistry, 2002
The cycloaddition of azides to alkynes is one of the most important synthetic routes to 1H-[1,2,3]-triazoles. Here a novel regiospecific copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes to azides on solid-phase is reported.
C. Tornøe, C. Christensen, M. Meldal
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The cycloaddition of azides to alkynes is one of the most important synthetic routes to 1H-[1,2,3]-triazoles. Here a novel regiospecific copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes to azides on solid-phase is reported.
C. Tornøe, C. Christensen, M. Meldal
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Angewandte Chemie, 2007
In 2001, Sharpless and co-workers introduced "click" chemistry, a new approach in organic synthesis that involves a handful of almost perfect chemical reactions.
Jean‐François Lutz
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In 2001, Sharpless and co-workers introduced "click" chemistry, a new approach in organic synthesis that involves a handful of almost perfect chemical reactions.
Jean‐François Lutz
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1,3-Dipolar Cycloadditions. Past and Future†
, 1963In contrast to the very large number of special methods applicable to syntheses in the heterocyclic series, relatively few general methods are available. The 1,3-dipolar addition offers a remarkably wide range of utility in the synthesis of five-membered
R. Huisgen
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