Results 161 to 170 of about 3,427 (216)

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

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

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

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

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Biginelli reaction: an overview

Tetrahedron Letters, 2016
Abstract Biginelli reaction involves acid-catalyzed one-pot synthesis of 3,4-dihydropyrimidin-2(1H)-ones (DHPMs) using easily-accessible starting materials, namely, aldehyde, active methylene compound and (thio)urea. DHPMs have stimulated resurgence of interest in the past two decades due to their wide ranging pharmacological activities and presence ...
Arindam Mukhopadhyay, Jarugu Narasimha Moorthy   +1 more
exaly   +2 more sources

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

2‐Phenacylbenzothiazole in the Biginelli Reaction.

ChemInform, 2002
AbstractFor Abstract see ChemInform Abstract in Full Text.
I. B. Dzvinchuk, T. V. Makitruk, M. O. Lozinskii   +2 more
openaire   +1 more source

An Inexpensive Protocol for Biginelli Reaction

Synthetic Communications, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
A. Manjula, B. Vittal Rao, Parvathi Neelakantan   +2 more
openaire   +1 more source