Results 151 to 160 of about 451,004 (214)

Eco-Friendly 1,3-Dipolar Cycloaddition Reactions on Graphene Quantum Dots in Natural Deep Eutectic Solvent. [PDF]

Nanomaterials (Basel), 2020
Giofrè SV, Tiecco M, Celesti C, Patanè S, Triolo C, Gulino A, Spitaleri L, Scalese S, Scuderi M, Iannazzo D.   +9 more
europepmc   +1 more source

Michael Addition - 1,3-dipolar Cycloaddition Reaction as an Easy Entry to Artificial Oligosaccharides

We report a novel approach for a synthesis of sugar clusters which is based on Michael addition/1,3-dipolar cycloaddition reaction ...
Lugiņina, Jevgeņija, Beļakovs, Sergejs, Turks, Māris, Rjabovs, Vitālijs   +3 more
core  

Study on Regio- and Diastereoselectivity of the 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylide with 2-(Benzo[d]thiazol-2-yl)-3-(aryl)acrylonitrile: Synthesis, Spectroscopic, and Computational Approach. [PDF]

ACS Omega
Hussein EM, Moussa Z, Al-Fahemi JH, Al-Rooqi MM, Obaid RJ, Malik MS, Abd-El-Aziz AS, Ahmed SA.   +7 more
europepmc   +1 more source

Ethynyl-substituted benzosiloxaboroles: the role of C(π)⋯B interactions in their crystal packing and use in Cu(i)-catalyzed 1,3-dipolar cycloaddition. [PDF]

RSC Adv
Pacholak P, Durka K, Woźniak K, Krajewska J, Laudy AE, Luliński S.   +5 more
europepmc   +1 more source

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Asymmetric 1,3-Dipolar Cycloaddition Reactions

Chemical Reviews, 1998
Karl Anker Jørgensen, Kurt V Gothelf
exaly   +3 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. Now, the structure, biosynthesis, and function of a heavily modified prenylated flavin cofactor have been elucidated.
Martin, Baunach, Christian, Hertweck
openaire   +2 more sources

Nanoparticle‐Catalysed 1,3‐Dipolar Cycloadditions

European Journal of Organic Chemistry, 2020
The 1,3‐dipolar cycloadditions of azomethine‐ylides and ‐imines, nitrones, nitrilimines, and azides catalysed by inorganic nanoparticles are described. Emphasis is given to the nanometric catalysts involved, their structure, characterisation, and recyclability and, when remarkable, their preparation.
Ponti A, Molteni G
openaire   +2 more sources

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   +1 more source

1,3-Dipolar Cycloadditions in Aqueous Media

HETEROCYCLES, 2006
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   +2 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.
Matthias, Müller, Cäcilia, Maichle-Mössmer, Holger F, Bettinger   +2 more
openaire   +2 more sources