Results 211 to 220 of about 43,074 (261)
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In Situ Generation of Nitrile Oxides from NaCl-Oxone Oxidation of Various Aldoximes and Their 1,3-Dipolar Cycloaddition.

Organic Letters, 2019
Reported is a new green protocol for the efficient in situ generation of nitrile oxides through NaCl/Oxone oxidation of aldoximes and their dipolar cycloaddition.
Guodong Zhao   +3 more
semanticscholar   +1 more source

ChemInform Abstract: Asymmetric 1,3‐Dipolar Cycloadditions of Acrylamides

ChemInform, 2010
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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.
Kissane, Marie, Maguire, Anita R.
openaire   +5 more sources

Stereo- and Regioselective 1,3-Dipolar Cycloaddition of the Stable Ninhydrin-Derived Azomethine Ylide to Cyclopropenes: Trapping of Unstable Cyclopropene Dipolarophiles.

Journal of Organic Chemistry, 2019
A stereo- and regioselective 1,3-dipolar cycloaddition of the stable ninhydrin-derived azomethine ylide [2-(3,4-dihydro-2 H-pyrrolium-1-yl)-1-oxo-1 H-inden-3-olate, DHPO] to differently substituted cyclopropenes has been established.
A. Filatov   +6 more
semanticscholar   +1 more source

ChemInform Abstract: 1,3‐Dipolar Cycloadditions to Allenes

ChemInform, 1996
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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.
BROGGINI, GIANLUIGI   +1 more
openaire   +3 more sources

ChemInform Abstract: 1,3‐Dipolar Cycloadditions to Oxidopyraziniums.

ChemInform, 1987
Abstract 1,5-Dimethyl-3-oxidopyrazinium (6) undergoes cycloadditions with methyl acrylate, acrylonitrile, diethyl maleate, maleimide, methyl propiolate and diethyl acetylenedicarboxylate.
Miklos Kiss   +2 more
openaire   +3 more sources

1,3-Dipolare Cycloaddition

1994
Von Huisgen 1,2) wurde 1963 die 1,3-dipolare Cycloaddition 3–5) als Reaktionsprinzip zum Aufbau von Heterocyclen systematisiert. Man versteht darunter die Addition eines 1,3-Dipols 1, der aus den verschiedenen Kombinationen von Kohlenstoff-, Stickstoff- und Sauerstoffatomen bestehen kann und vier nicht dienische π-Elektronen umfast, an eine ...
Thomas Laue, Andreas Plagens
openaire   +2 more sources

Transition Metal Complexation in 1,3-Dipolar Cycloadditions

HETEROCYCLES, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
BROGGINI, GIANLUIGI   +3 more
openaire   +5 more sources

Synthesis of Spiro[oxindole-3,2'-pyrrolidine] Derivatives from Benzynes and Azomethine Ylides through 1,3-Dipolar Cycloaddition Reactions.

Journal of Organic Chemistry, 2018
A novel synthetic strategy employing benzyne and azomethine ylides for the construction of spiro[oxindole-3,2'-pyrrolidine] derivatives has been achieved in good yields.
Heesun Ryu, J. Seo, H. Ko
semanticscholar   +1 more source

Asymmetric 1,3-dipolar cycloadditions

Tetrahedron, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
openaire   +3 more sources

Boryl Azides in 1,3-Dipolar Cycloadditions

The Journal of Organic Chemistry, 2014
The 1,3-dipolar cycloaddition reaction of boron azides with alkynes has been investigated experimentally and computationally. At room temperature pinBN3 (pin = pinacolato) reacts with the strained triple bond of cyclooctyne with formation of an oligomeric boryl triazole.
Holger F. Bettinger   +2 more
openaire   +3 more sources

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