Results 141 to 150 of about 13,198 (167)

<i>N</i>‑Iminopyridinium Ylides as Chemically Stable Pharmacophores Enabling Targeted Degradation of SMARCA Proteins. [PDF]

JACS Au
Zhang S, Zhang X, Lou J, Jing H, Yan Z, Wang Y, Gui Y, Xu L, Lyu X, Lu Y, Wang Z, Liu C, Xiao X, Meng L, Zhao Y.   +14 more
europepmc   +1 more source

Fused-Linked and Spiro-Linked N-Containing Heterocycles. [PDF]

Int J Mol Sci
Moskalik MY, Shainyan BA.
europepmc   +1 more source

Formal nitrogen-to-carbon replacement in isoindolines to form indenes <i>via N</i>-alkyl tetrahydroisoquinolines. [PDF]

Chem Sci
Steele RT, Domack J, Sarpong R.
europepmc   +1 more source

Mechanistic insights into the (3 + 2) cycloaddition of azomethine ylide with dimethyl acetylenedicarboxylate <i>via</i> bond evolution theory. [PDF]

RSC Adv
Chellegui M, Al-Mokhtar RM, Salih RN, Benhamed L, Benmetir S, Vicente de Julián-Ortiz J, Mohammad-Salim HA, Ben Ahmed A.   +7 more
europepmc   +1 more source

Dispiroindolinone-Glutarimide Conjugates: Synthesis and Evaluation as Potential Hetero-PROTACs for p53 Reactivation. [PDF]

Molecules
Polyakov VS, Grishin YK, Tafeenko VA, Ivanova ES, Pogodaeva SS, Moldavskii DV, Shtil AA, Beloglazkina EK.   +7 more
europepmc   +1 more source

Advances in the biomimetic and Maillard route synthesis and regulation of pyrazine flavour compounds. [PDF]

RSC Adv
Wang B, Zhao Y, Zhao L, Zhu W, Ren J.
europepmc   +1 more source

Transforming the Buckyball: Regioselective Synthesis of Water-Soluble [60]Fullerene Derivatives for Biomedical Applications. [PDF]

Molecules
Kraevaya OA, Troshin PA.
europepmc   +1 more source

Enantioselective Copper-Catalyzed [3+3] Cycloaddition of Azomethine Ylides With Azomethine Imines

Angewandte Chemie - International Edition, 2013
Enantioselective Copper-Catalyzed [3+3] Cycloaddition of Azomethine Ylides with Azomethine ...
Risong Na, Hui Jiang, Hongchao Guo
exaly   +2 more sources

Conjugated Azomethine Ylides [PDF]

European Journal of Organic Chemistry, 2006
The 1,3-dipolar cycloaddition of azomethine ylides is an efficient and versatile tool for the construction of five-membered nitrogen-heterocycles. When the azomethine ylide is conjugated with a double bond or a 1,3-diene moiety, other reactivity pathways

exaly   +2 more sources

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Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

Chemical Reviews, 2005
Iain Coldham
exaly