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Decarboxylation-Driven Double Annulations: Innovative Multi-Component Reaction Pathways [PDF]
A concerted five-component reaction strategy has been developed, featuring double [3+2] cycloadditions utilizing aspartic acid. This approach provides valuable insights into mechanistic pathways, allowing for the distinction between concerted and ...
Desheng Zhan +4 more
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Department of Chemistry, Laboratory of Macromolecular and Organic Chemistry, University of Louvain, B-3030 Heverlee, Belgium Received 4 September 1972 Thennostable poly-1,2,3-triazoles (7) were prepared by the regiospecific rt:action of bisazides with. keto-stabilhed bisalkylidenephosporanes (6) in DMSO solution.
Pierre A Ykman, G. L' ABBE, G. SMETS
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The one-pot [3 + 2] cycloaddition of an azomethine ylide with a maleimide followed by another [3 + 2] cycloaddition of an azide with the second maleimide gives a 1,5-diamino intermediate which is used for a sequential aminomethylation reaction with ...
Xiaofeng Zhang +6 more
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1, 3-Dipolar Cycloaddition of Furancarbonitrile Oxide with Olefins
Tadashi Sasaki
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Structure, liquid and solid state synthesis for dimers via [3+3] dipolar cycloadditions [PDF]
Gheorghita N. Zbancioc +3 more
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Gram Scale Synthesis of (±)-Gregatin A via 1, 3-dipolar Cycloaddition Strategy [PDF]
Yiming Ding +7 more
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[3+2] Cycloaddition of alkyl aldehydes and alkynes enabled by photoinduced hydrogen atom transfer
In contrast to the prevalence of 1,3-dipolar cycloadditions, radical [3+2] annulations of alkynes are underexplored. Here, the authors describe [3+2] cycloadditions of various internal alkynes with readily accessible aliphatic aldehydes via photoinduced ...
Siya Le +6 more
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Studies on the [2+3] cycloaddition reaction of nitrile oxides to abietic acid esters [PDF]
[2+3] Dipolar cycloadditions of aromatic nitrile oxides to abietic acid esters were investigated. The reactions showed complete site selectivity and regioselectivity, while the stereoselectivity depended on the structures of the dipolarophiles.
Gucma Mirosław +3 more
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Reaction profiles for quantum chemistry-computed [3 + 2] cycloaddition reactions
Bio-orthogonal click chemistry based on [3 + 2] dipolar cycloadditions has had a profound impact on the field of biochemistry and significant effort has been devoted to identify promising new candidate reactions for this purpose.
Thijs Stuyver +2 more
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Discovery of new mutually orthogonal bioorthogonal cycloaddition pairs through computational screening. [PDF]
Density functional theory (DFT) calculations and experiments in tandem led to discoveries of new reactivities and selectivities involving bioorthogonal sydnone cycloadditions.
Houk, KN +3 more
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