Results 101 to 110 of about 22,593 (123)

Targeted 1,3-dipolar cycloaddition with acrolein for cancer prodrug activation. [PDF]

Chem Sci, 2021
Pradipta AR, Ahmadi P, Terashima K, Muguruma K, Fujii M, Ichino T, Maeda S, Tanaka K.   +7 more
europepmc   +1 more source

1,3-Dipolar Cycloaddition and Mannich Reactions of Alkynyl Triterpenes: New Trends in Synthetic Strategies and Pharmacological Applications. [PDF]

Int J Mol Sci
Petrova AV, Kazakova OB.
europepmc   +1 more source

Correction: 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

1,3-Dipolar Cycloaddition of Nitrile Oxides and Nitrilimines to (-)-β-Caryophyllene: Stereoselective Synthesis of Polycyclic Derivatives and Their Biological Testing. [PDF]

Int J Mol Sci
Shybanov DE, Kukushkin ME, Grishin YK, Roznyatovsky VA, Tafeenko VA, Abo Qoura L, Pokrovsky VS, Yarovaya OI, Belyaevskaya SV, Volobueva AS, Esaulkova IL, Zarubaev VV, Zarubaev VV, Beloglazkina EK.   +13 more
europepmc   +1 more source

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

3-Benzoylisoxazolines by 1,3-Dipolar Cycloaddition: Chloramine-T-Catalyzed Condensation of α-Nitroketones with Dipolarophiles. [PDF]

Molecules, 2021
Pan X, Xin X, Mao Y, Li X, Zhao Y, Liu Y, Zhang K, Yang X, Wang J.   +8 more
europepmc   +1 more source

Lewis Acid-Catalyzed 1,3-Dipolar Cycloaddition of Bicyclobutanes with Isatogens: Access to Tetracyclic 2-Oxa-3-azabicyclo[3.1.1]heptanes. [PDF]

JACS Au
Deswal S, Das RC, Sarkar D, Biju AT.
europepmc   +1 more source

How the Lewis Base F^- Catalyzes the 1,3-Dipolar Cycloaddition between Carbon Dioxide and Nitrilimines. [PDF]

J Org Chem, 2021
Svatunek D, Hansen T, Houk KN, Hamlin TA.   +3 more
europepmc   +1 more source

Acceleration and Selectivity of 1,3-Dipolar Cycloaddition Reactions Included in a Polar [4 + 2] Octa-imine Bis-calix[4]pyrrole Cage. [PDF]

JACS Au
Li Y, Mirabella CFM, Aragay G, Ballester P.   +3 more
europepmc   +1 more source

Asymmetric Synthesis of Tetrahydroisoquinoline Derivatives through 1,3-Dipolar Cycloaddition of C,N-Cyclic Azomethine Imines with Allyl Alkyl Ketones. [PDF]

Molecules, 2021
Feng G, Ma G, Chen W, Xu S, Wang K, Wang S.   +5 more
europepmc   +1 more source