Results 201 to 210 of about 4,540 (259)

Competitive cyclization of ethyl trifluoroacetoacetate and methyl ketones with 1,3-diamino-2-propanol into hydrogenated oxazolo- and pyrimido-condensed pyridones. [PDF]

Beilstein J Org Chem
Kushch SO, Goryaeva MV, Burgart YV, Ezhikova MA, Kodess MI, Slepukhin PA, Volobueva AS, Zarubaev VV, Saloutin VI.   +8 more
europepmc   +1 more source

A retrospective 9-years overview of sulfated polyborate as a robust catalyst for organic transformations. [PDF]

RSC Adv
Chhaperwal P, Soni S, Teli S, Rundla HK, Agarwal S.   +4 more
europepmc   +1 more source

Structural reassignment of compound 968, an allosteric glutaminase inhibitor. [PDF]

Beilstein J Org Chem
Albertelli LA, Jallow S, Li C, Ulrich SM.   +3 more
europepmc   +1 more source

An Environmentally Friendly Solvent-free Synthesis of 3,4-Dihydropyrimidinones using a p -Aminobenzene Sulfonic Acid Catalyzed Biginelli Reaction

, 2010
Ming Shu Wu, Ping He, Xiang Zhu Zhang
openalex   +1 more source

Innovative synthesis of antimicrobial Biginelli compounds using a recyclable iron oxide-based magnetic nanocatalyst. [PDF]

Sci Rep
Taravati A, Nouri M, Poursattar Marjani A, Akbari Dilmaghani K.   +3 more
europepmc   +1 more source

Synthesis of some new pyrimidine-based pyrene/benzochromene hybrids as EGFR kinase inhibitors in HCT-116 cancer cells through apoptosis. [PDF]

RSC Adv
Mohammed YAA, Kheder NA, Nafie MS, Abbas AA, Dawood KM.   +4 more
europepmc   +1 more source

Once Upon a Time Without DMF: Greener Paths in Peptide and Organic Synthesis. [PDF]

Molecules
Scognamiglio A, Magli E, Caliendo G, Perissutti E, Santagada V, Severino B.   +5 more
europepmc   +1 more source

Designing and the anticancer activity of chitosan and chitosan oligosaccharide lactate nanobeads loaded with Biginelli hybrid. [PDF]

RSC Adv
Janković N, Ristovski J, Žižak Ž, Radan M, Cvijić S, Nikolić K, Ignjatović NL.   +6 more
europepmc   +1 more source

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The Biginelli Reaction

Journal of Chemical Education, 2001
The utilization of the Biginelli reaction, a one-pot condensation of an aldehyde, a β-keto ester, and urea, is described. This reaction involves a number of individual steps, each of which is accessible to first-year organic students. The product, a 3,4-dihydropyrimidinone, is a member of a medicinally useful class of compounds.
Michael S. Holden, R. David Crouch
openaire   +1 more source