1,3-dipolar cycloadditions - Open Access .click

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Relative Rates of Metal-Free Azide-Alkyne Cycloadditions: Tunability over 3 Orders of Magnitude. [PDF]

, 2019
The thermal (3 + 2) dipolar azide-alkyne cycloaddition, proceeding without copper or strained alkynes, is an underutilized ligation with potential applications in materials, bioorganic, and synthetic chemistry.
Braslau, Rebecca +6 more
core

Theoretical Study of 1,3-Dipolar Cycloadditions Regioselectivity of Benzyl Azide with Glycosyl-O Acetylene Using Density Functional Theory (DFT)

Orbital: The Electronic Journal of Chemistry, 2017
A theoretical study of 1,3-cycloaddition has been carried out using density functional theory (DFT) methods at the B3LYP/6-31G* level. The regioselectivity of the reaction have been clarified through different theoretical approaches: Case of a Two-Center
Adib Ghaleb +5 more
doaj

Mechanistic impact of oxime formation accompanying 1,3-dipolar cycloadditions of nitrile oxides [PDF]

, 1989
Baran, Janusz, Mayr, Herbert
core +1 more source

1,3-Dipolar cycloadditions of acridine with nitrile oxides

ARKIVOC, 2002
Antonino Corsaro +5 more
doaj +1 more source

Studies on 1,3-dipolar cycloadditions

, 2000
Centre of Advanced Studies on Natural Products, Department of Chemistry, University of Calcutta, 92 Acharya Prafulla Chandra Road, Calcutta-700 009, India E-mail : ab@cucc.ernet.in Manuscript received 2 November 2000 Studies on 1,3-dipolar ...
openaire +1 more source

Synthesis and spectroscopic and structural characterization of spiro[indoline-3,3'-indolizine]s formed by 1,3-dipolar cycloadditions between isatins, pipecolic acid and an electron-deficient alkene. [PDF]