Results 151 to 160 of about 99,145 (214)

The Huisgen Reaction: Milestones of the 1,3-Dipolar Cycloaddition. [PDF]

Angew Chem Int Ed Engl, 2020
Breugst M, Reissig HU.
europepmc   +1 more source

Theoretical Study of the Mechanism of the Formation of Azomethine Ylide from Isatine and Sarcosine and Its Reactivity in 1,3-Dipolar Cycloaddition Reaction with 7-Oxabenzonorbornadiene. [PDF]

Int J Mol Sci
Antol I, Štrbac P, Murata Y, Margetić D.   +3 more
europepmc   +1 more source

Atroposelective Synthesis of Axially Chiral Naphthylpyrroles by a Catalytic Asymmetric 1,3-Dipolar Cycloaddition/Aromatization Sequence. [PDF]

Org Lett
Maclean I, Gallent E, Orozco O, Molina A, Rodríguez N, Adrio J, Carretero JC.   +6 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  

Density Functional Theory Calculations: A Useful Tool to Investigate Mechanisms of 1,3-Dipolar Cycloaddition Reactions. [PDF]

Int J Mol Sci
Chiacchio MA, Legnani L.
europepmc   +1 more source

Diazomethyl-λ³-iodane meets aryne: dipolar cycloaddition and C-to-N iodane shift leading to indazolyl-λ³-iodanes. [PDF]

Chem Sci
Otsuki S, Kanemoto K, Martos DC, Kwon E, Wencel-Delord J, Yoshikai N.   +5 more
europepmc   +1 more source

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