Results 151 to 160 of about 24,842 (217)

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

Heterohelicenes through 1,3-Dipolar Cycloaddition of Sydnones with Arynes: Synthesis, Origins of Selectivity, and Application to pH-Triggered Chiroptical Switch with CPL Sign Reversal. [PDF]

JACS Au, 2021
Yen-Pon E, Buttard F, Frédéric L, Thuéry P, Taran F, Pieters G, Champagne PA, Audisio D.   +7 more
europepmc   +1 more source

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

Solvent-free synthesis of 3,5-isoxazoles via 1,3-dipolar cycloaddition of terminal alkynes and hydroxyimidoyl chlorides over Cu/Al₂O₃ surface under ball-milling conditions. [PDF]

RSC Adv, 2022
Hernandez R RA, Burchell-Reyes K, Braga APCA, Lopez JK, Forgione P.   +4 more
europepmc   +1 more source

Covalent organic functionalization of graphene nanosheets and reduced graphene oxide via 1,3-dipolar cycloaddition of azomethine ylide. [PDF]

Nanoscale Adv, 2021
Basta L, Moscardini A, Fabbri F, Bellucci L, Tozzini V, Rubini S, Griesi A, Gemmi M, Heun S, Veronesi S.   +9 more
europepmc   +1 more source

The Rich Chemistry Resulting from the 1,3‐Dipolar Cycloaddition Reactions of Enamines and Azides

, 2018
V. Bakulev, T. Beryozkina, Joice Thomas, W. Dehaen   +3 more
semanticscholar   +1 more source

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

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

Telodendrimer-Based Macromolecular Drug Design using 1,3-Dipolar Cycloaddition for Applications in Biology. [PDF]

Molecules, 2020
Yazdani H, Kaul E, Bazgir A, Maysinger D, Kakkar A.   +4 more
europepmc   +1 more source

Highly regioselective 1,3-dipolar cycloaddition of 3'-O-propargyl guanosine with nitrile oxide: An efficient method for the synthesis of guanosine containing isoxazole moiety. [PDF]

Tetrahedron Lett, 2020
Shanmugasundaram M, Senthilvelan A, Kore AR.   +2 more
europepmc   +1 more source