Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 34 checked references that resolve
resolves10.1016/j.ejmech.2017.12.004Design, synthesis, biological evaluation and cocrystal structures with tubulin of chiral β -lactam bridged combretastatin A-4 analogues as potent antitumor agents
resolves10.1039/C8MD00147BSynthesis and biological evaluation of new 3-amino-2-azetidinone derivatives as anti-colorectal cancer agents
resolves10.1021/jm0255825Stereoselective Synthesis of β-Lactams with Polyaromatic Imines: Entry to New and Novel Anticancer Agents
resolves10.1021/cr0307300β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products
resolves10.1007/7081_2009_11β-Lactam Ring Opening: A Useful Entry to Amino Acids and Relevant Nitrogen-Containing Compounds
resolves10.1021/jo061339sSynthesis of Docetaxel and Butitaxel Analogues through Kinetic Resolution of Racemic β-Lactams with 7-<i>O</i>-Triethylsilylbaccatin III
resolves10.1002/ps.4330Review of anthraquinone applications for pest management and agricultural crop protection
resolves10.1039/C9MD00258HDevelopment of benzochalcone derivatives as selective CYP1B1 inhibitors and anticancer agents
resolves10.1039/C9MD00242ASynthesis and anti-cancer activities of glycosides and glycoconjugates of diterpenoid isosteviol
resolves10.1016/j.bioorg.2019.103515Synthesis, in vitro biological evaluation and in silico molecular docking studies of novel β-lactam-anthraquinone hybrids
resolves10.1007/s11030-005-1306-xA structurally diverse heterocyclic library: A benzothiazepine-fused ? -lactam library derived from reaction of 2,3-dihydro-1,5-benzothiazepines and acyl chlorides: Synthesis and stereochemistry
resolves10.1016/j.bioorg.2019.102928Synthesis of novel Schiff bases and azol-β-lactam derivatives starting from morpholine and thiomorpholine and investigation of their antitubercular, antiurease activity, acethylcolinesterase inhibition effect and antioxidant capacity
resolves10.1021/cr4005549Chemical Synthesis of β-Lactams: Asymmetric Catalysis and Other Recent Advances
resolves10.1016/j.tetlet.2014.07.089A straightforward approach to 2-azetidinones from imines and carboxylic acids using dimethyl sulfoxide and acetic anhydride
resolves10.1016/j.ejmech.2011.04.039Retraction notice to “2-Azetidinone derivatives: Design, synthesis, in vitro anti-microbial, cytotoxic activities and DNA cleavage study”, European Journal of Medicinal Chemistry (2009) 5123–5130
resolves10.1007/s00706-014-1217-6An efficient and green method for the synthesis of 2-azetidinones mediated by propylphosphonic anhydride (T3P®)
resolves10.1016/j.ejmech.2014.09.077Diastereoselective synthesis of potent antimalarial cis-β-lactam agents through a [2 + 2] cycloaddition of chiral imines with a chiral ketene
resolves10.1016/j.tet.2012.04.011Synthesis of novel β-lactams bearing an anthraquinone moiety, and evaluation of their antimalarial activities
The 3 references without a DOI — listed, not checked
no DOI — not checkedMorin RB, Gorman M (eds) (1982) Chemistry and biology of β-lactam antibiotics, vol 1-3. Academic Press, New York
no DOI — not checkedSilverman RB (2004) The organic chemistry of drug design and drug action, 2nd edn. Amsterdam, Elsevier
no DOI — not checkedZollinger H (1991) Colour chemistry, synthesis, properties and applications of organic dyes and pigments. VCH Publishers, New York
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