Relevant bibliographies by topics / Azetidinones

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Azetidinones'

Author: Grafiati
Published: 5 June 2025
Last updated: 15 July 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Azetidinones.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Azetidinones"

1

Alcaide, Benito, Pedro Almendros, Teresa Martínez del Campo, and Teresa Naranjo. "Gold-catalyzed preparation of annelated 2-azetidinones via divergent heterocyclization of enyne-tethered oxazolidines." Organic Chemistry Frontiers 5, no. 5 (2018): 817–21. http://dx.doi.org/10.1039/c7qo00950j.

Full text
Abstract:
The divergent and selective syntheses of two types of annelated β-lactams, namely, furan- and tetrahydropyridine-fused 2-azetidinones, have been accomplished directly from 2-azetidinone-tethered oxazolidine-enynes through gold catalysis.
APA, Harvard, Vancouver, ISO, and other styles
2

Baruah, Shyamal, Amrit Puzari, Farhana Sultana, and Jayanta Barman. "Synthesis, Characterization and Evaluation of Antimicrobial Properties of (R)-(-)-4-Phenyl-2 Oxazolidinone Based Azetidinones." Anti-Infective Agents 16, no. 2 (2018): 104–13. http://dx.doi.org/10.2174/2211352516666180619153317.

Full text
Abstract:
Introduction: A series of (R)-(-)-4-Phenyl-2 oxazolidinone based azetidinones (4a-i) were synthesized from the reaction of (2-Oxo-4-phenyl-oxazolidin-3-yl) acetic acid with aromatic imines (3a-i) in the presence of Thionyl chloride and Triethylamine as a base. Methods: The transformation proceeds through the formation of acid chloride to ketene which finally forms the azetidinones through [2+2] cycloaddition with aromatic imines. Products obtained were screened to evaluate their antibacterial activity with respect to known bacteria like Escherichia Coli (E. Coli) and Bacillus subtilis. Results
APA, Harvard, Vancouver, ISO, and other styles
3

AL-Tamimi, Entesar Obeed, Raad Mahjoub Muslih, and Khalida Ali Thejeel. "Synthesis, Characterization and Antibacterial Studies of 2-azetidinones Compounds Derived from Amoxicillin." Al Mustansiriyah Journal of Pharmaceutical Sciences 15, no. 1 (2015): 14–23. http://dx.doi.org/10.32947/ajps.v15i1.160.

Full text
Abstract:
In this study, the new azetidinones were synthesized from Schiff bases 2(a-j) that derived from amoxicillin (1) on treatment with chloroacetyl chloride in presence of triethylamine gave azetidinone 3(a-j). The structure of these compounds have been elucidated on the basis of their physical and spectral. Azetidinone compounds were also screened for their antibacterial activity against some bacterial species using amoxicillin as standard.
APA, Harvard, Vancouver, ISO, and other styles
4

Sakarya, Handan Can, and Aslı Ketrez. "Synthesis of Novel cis-2-Azetidinones from Imines and Chloroacetyl Chloride Using Triethylamine." Acta Chimica Slovenica 70, no. 4 (2023): 628–33. http://dx.doi.org/10.17344/acsi.2023.8451.

Full text
Abstract:
A synthesis of a novel series of cis-2-azetidinones 2a–c was carried out by the cycloaddition reaction of imine 1a–c and chloroacetyl chloride in dry dichloromethane at 0–5 °C using triethylamine. The cycloaddition of the Schiff bases with chloroacetyl chloride resulted in the corresponding major product cis-2-azetidinone stereoisomers 2a–c. The synthesized compounds were characterized by analytical and spectral techniques (infrared, 1H NMR, 13C NMR, and elemental analysis).
APA, Harvard, Vancouver, ISO, and other styles
5

Bhat, Ishwar, Sunil Chaithanya, P. D. Satyanarayana, and Balakrishna Kalluraya. "The synthesis and antimicrobial study of some azetidinone derivatives with the para-anisidine moiety." Journal of the Serbian Chemical Society 72, no. 5 (2007): 437–42. http://dx.doi.org/10.2298/jsc0705437b.

Full text
Abstract:
Azetidinones were synthesized from p-anisidine in two steps. First the Schiff's bases were prepared by reacting the hydrazide of an anisidine derivative with different aromatic aldehydes. Cyclocondensation of the Schiff's bases with chloroacetyl chloride in the presence of triethylamine resulted in the formation of the corresponding azetidinone analogues. The structures of the newly synthesized compounds were confirmed by IR, 1H NMR and mass spectroscopic analysis. The antibacterial and antifungal potential of the synthesized compounds were evaluated by the agar disc method.
APA, Harvard, Vancouver, ISO, and other styles
6

Tamador A. Mahmood. "Synthesis of new N-Substituted -3- chloro -2- azetidinones for 2, 4-Diamino-6-phenyl-1,3,5-triazine." Journal of the College of Basic Education 21, no. 88 (2023): 1–12. http://dx.doi.org/10.35950/cbej.v21i88.9948.

Full text
Abstract:
The current study involved synthesis of several new N-Substituted -
 3- chloro -2- azetidinones for 2,4-Diamino-6-phenyl-1,3,5-triazine by two
 steps. The first step includes preparation of Schiff bases (Al-A6) by
 condensation of 2,4-Diamino-6-pheny]-1,3,5-triazine with many substituted
 aldehydes, then the second step includes preparation new six azetidinone
 compounds (B1-B6) by reaction of chloro acetyl chloride with the
 prepared Schiff bases in first step. The prepared compounds were
 characterized by physical properties, FT-IR, UV and some of them by '
APA, Harvard, Vancouver, ISO, and other styles
7

Zarei, Maaroof. "Cerium(IV) Tetrabutylammonium Nitrate (CTAN): A Mild and Efficient N-dearylation Agent for Synthesis of N-unsubstituted 2-azetidinones." Journal of Chemical Research 41, no. 4 (2017): 246–49. http://dx.doi.org/10.3184/174751917x14902201357392.

Full text
Abstract:
A simple and efficient protocol for the conversion of N-p-methoxyphenyl, N-p-ethoxyphenyl, N-p-methoxynaphthyl, N-3,4-dimethoxybenzyl and N-p-methoxybenzyl-2-azetidinones to N-unsubstituted 2-azetidinones using cerium(IV) tetrabutylammonium nitrate (CTAN) in dichloromethane is described. The method is compatible with a number of functional groups, and N-unsubstituted 2-azetidinones can be prepared under mild conditions at room temperature. The reaction is rapid, and pure products are obtained in good yields.
APA, Harvard, Vancouver, ISO, and other styles
8

Govindarao Kamala, Sri Laya A, Sri Nandini G, et al. "Quinoline Based 2-Azetidinones, 4-Thiazolidinones and Their Potential Pharmacological Activities." Journal of Pharma Insights and Research 2, no. 4 (2024): 107–24. http://dx.doi.org/10.69613/r73gtb07.

Full text
Abstract:
Globally, many diseases with unmet therapeutic needs persist, including cancer, tuberculosis, and various infectious diseases. The rapid development of new drugs is crucial to counteract these health challenges. Medicinal chemists, in collaboration with other scientists, continuously strive to design and develop novel lead molecules with potential therapeutic applications. Molecular hybridization is a common approach in this field, often resulting in the synthesis of new compounds with synergistic or novel activities. Quinoline-based hybrid molecules, particularly those incorporating 2-azetidi
APA, Harvard, Vancouver, ISO, and other styles
9

Just, George, and Guerino Sacripante. "Synthesis of tricyclic azetidinones by intramolecular free radical cyclization." Canadian Journal of Chemistry 65, no. 1 (1987): 104–9. http://dx.doi.org/10.1139/v87-017.

Full text
Abstract:
The synthesis of strained tricyclic azetidinones was achieved by free radical cyclization of N-substituted azetidinones involving a tributyltin hydride/AIBN mediated chain reaction. The 5-exo cyclization led to benzo carbapenems 10, 12, and 13, which were relatively unstable in solution. The 6-exo mode, however, afforded stable benzo carbacephems 20, 22, 24, and 25.
APA, Harvard, Vancouver, ISO, and other styles
10

V., K. SRIVASTAVA, PALIT G., SINGH S., DHAWAN R., and SHANKER K. "Thiouryl F ormazan, Thiazolidinone and. Azetidinone Derivatives as Antiparkinsonian Agents." Journal of Indian Chemical Society Vol. 67, April 1990 (1990): 335–38. https://doi.org/10.5281/zenodo.6163513.

Full text
Abstract:
Department of Pharmacology and Therapeutics, K. G. s Medical College, Lucknow-226 003 <em>Manuscript received 8 March 1989, revised 9 August 1989, accepted&nbsp;21 November 1989</em> Substituted thiouryl formazans, thiazolidinones and azetidinones were synthesised and their antiparkinsonian&nbsp;activity was studied. The study showed that thiouryl formazans derivative&nbsp;having dimethylamino and chloro group, thouryl thiazolidinones and azetidinones having phenyl, 4--methoxyphenyl group at 2nd and 4th position were found most potent. Some compounds showed lesser toxicity. &nbsp; &nbsp;
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Azetidinones"

1

Sharma, Madan Kumar. "Approaches to 3,3-disubstituted azetidinones." Thesis, University of Ottawa (Canada), 1990. http://hdl.handle.net/10393/5577.

Full text
Abstract:
Chapter 1 contains a very brief overview of 3,3-disubstituted azetidinones. Also included in this chapter are the approaches to 'hybrid' azetidinones, i.e. those which contain the structural features of more than one class of azetidinones. Finally the target molecules for the present studies are listed. Chapter 2 contains details of use of various 2,3-dihydroxybutyric acid derivatives in enantioselective syntheses of 3-alkoxyazetidinones with an additional substituent at position 3. In chapter 3 similar studies on threonine derivatives for the syntheses of 3-amino-3-hydroxyethylazetidinones ar
APA, Harvard, Vancouver, ISO, and other styles
2

Burtoloso, Antonio Carlos Bender. "3-azetidinonas e 3-azetidinois : preparação e aplicações na sintese de azetidinas substituidas." [s.n.], 2006. http://repositorio.unicamp.br/jspui/handle/REPOSIP/249762.

Full text
Abstract:
Orientador: Carlos Roque Duarte Correia<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-08-05T22:30:16Z (GMT). No. of bitstreams: 1 Burtoloso_AntonioCarlosBender_D.pdf: 10110814 bytes, checksum: 1e36973f12232933308e658cdad952fe (MD5) Previous issue date: 2006<br>Doutorado<br>Quimica Organica<br>Doutor em Ciências
APA, Harvard, Vancouver, ISO, and other styles
3

ADONIAS, MIREILLE. "Synthese de 2-azetidinones trisubstituees inhibiteurs potentiels d'elastases. Nouvelles voie d'acces radicalaire a des cycles carbapenames et carbapenemes." Paris 11, 1993. http://www.theses.fr/1993PA112324.

Full text
Abstract:
Cette these decrit la synthese enantioselective de beta-lactames utilisant la reaction de staudinger, avec la d-glucosamine comme auxiliaire chiral. Le chapitre i concerne la synthese de monobactames 1,3,4-trisubstitues dont l'etape cle est une reaction de cycloaddition 2+2 entre un cetene et une imine. Le cetene genere a partir de l'acide methoxy acetique ou de l'acide hexanoique, reagit avec une base de schiff chirale obtenue par condensation entre le 3,4;5,6-di-o-isopropylidene 1-propane dithioacetal d-glucosamine et le cinnamaldehyde, ou le methyl-cinnamaldehyde. Les beta-lactames monocycl
APA, Harvard, Vancouver, ISO, and other styles
4

O'Gorman, P. A. "Some aspects of the chemistry of small ring organic molecules : 1-azetines, 1-azetidinones, 3-oxo-β-sultams and cyclopropenones". Thesis, University of Huddersfield, 2009. http://eprints.hud.ac.uk/id/eprint/6310/.

Full text
Abstract:
The -lactams and the related -sultams are attractive targets for synthesis because of their central importance in antibiotics such as the penicillins. These heterocycles are of further interest because of their potential as inhibitors of the serine protease class of enzymes113, believed to be responsible for diseases such as rheumatoid arthritis and cystic fibrosis. This thesis will describe the synthesis of the 4-vinyl beta lactams (A)25, thiation of these compounds using Lawesson’s reagent to yield thio lactams (B) and subsequent conversion into the corresponding 1-azetine (C) using Meerwe
APA, Harvard, Vancouver, ISO, and other styles
5

Shimamoto, Yasuhiro. "Exploration of New Reactivities of Azetidinols and Alkynylborates." 京都大学 (Kyoto University), 2014. http://hdl.handle.net/2433/188616.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Gollins, David William. "The use of 2-azetidinone-4-carboxylic acid as a chiral synthon." Thesis, University of Oxford, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386889.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Silva, Junior Jose Antunes da. "Estudo da reatividade de 1-azirinas-3-funcionalizadas frente a difenilceteno-sintese de novas 2-pirrolonas e 2-azetidinonas derivadas." [s.n.], 1996. http://repositorio.unicamp.br/jspui/handle/REPOSIP/250599.

Full text
Abstract:
Orientador: Albert James Kascheres<br>Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-07-22T06:57:36Z (GMT). No. of bitstreams: 1 SilvaJunior_JoseAntunesda_D.pdf: 6047431 bytes, checksum: 6ac6494cd056b3d8851771ceb02674ff (MD5) Previous issue date: 1996<br>Doutorado
APA, Harvard, Vancouver, ISO, and other styles
8

ABBIATI, GIORGIO. "Reazioni di cicloaddizione tra 1,3-diazabuta-1,3-dieni e cheteni:sintesi di diidropirimidinoni e 4-immino-azetidinoni." Doctoral thesis, Università degli Studi di Milano, 2000. http://hdl.handle.net/2434/651275.

Full text
Abstract:
The work of this Ph.D. thesis is an in depth study on [4+2] and [2+2] cycloaddition reactions of 1-(4-methylphenyl) and 1-benzyl-1,3-diaza-1,3-butadienes with different ketenes, usually generated from the corresponding acid halide in the presence of a base. Reaction with phenyl, diphenyl, chloro and ethoxycarbonylketenes are described and the mechanism involved is discussed. Moreover, thermal and photochemical ring expansion reactions of azetidinones to 5,6-dihydro-3H-pyrimidin-4-ones are studied. Finally, the [2+2] cycloaddition reactions of 1-benzyl-2,4-diphenyl-1,3-diaza-1,3-butadiene with
APA, Harvard, Vancouver, ISO, and other styles
9

Nobre, Cintia Maria Rubo de Souza. "Adição de IN3 a derivados de acidos -alquil cinamicos : obtenç2o de 2-alquil-3-fenil-1-azirinas e 3-azido-2-azetidinonas." [s.n.], 1987. http://repositorio.unicamp.br/jspui/handle/REPOSIP/250489.

Full text
Abstract:
Orientador : Albert James Kascheres<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Quimica<br>Made available in DSpace on 2018-07-17T03:51:17Z (GMT). No. of bitstreams: 1 Nobre_CintiaMariaRubodeSouza_M.pdf: 5224874 bytes, checksum: 477c2718ef7c65ea238a8cd7606090a1 (MD5) Previous issue date: 1987<br>Mestrado
APA, Harvard, Vancouver, ISO, and other styles
10

Murphy, Deirdre M. "STUDIES OF THE METALLO BETA LACTAMASE CCrA FROM BACTERIODES FRAGILIS AND A DANSYLATED MONOCYCLIC BETA LACTAM (1-(5-DIMETHYLAMINO-1-NAPTHALENESULFONYL HYDRAZIDO)-3-ACETAMIDO-4-METHOXY-2-AZETIDINONE." University of Cincinnati / OhioLINK, 2001. http://rave.ohiolink.edu/etdc/view?acc_num=ucin990561318.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Azetidinones"

1

Alcaide, Benito, Pedro Almendros, and Amparo Luna. "The Chemistry of 2-Azetidinones (β-Lactams)." In Modern Heterocyclic Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527637737.ch24.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "31 C3H5NO 2-Azetidinone." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_32.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Demaison, J. "307 C3H5NO 2-Azetidinone." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_55.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Prieto, A., J. I. Iribarren, S. Muñoz-Guerra, C. Bui, and H. Sekiguchi. "Structural Study on the Chiral Nylon-3, Poly(3,3-Ethyl Phenyl-2-Azetidinone)." In Crystallization of Polymers. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1950-4_65.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

BATESON, JOHN H. "Asymmetric Synthesis of Azetidinones." In A Critical Review of the 1990 Literature Preceded by Two Chapters on Current Heterocyclic Topics. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-08-040589-6.50006-0.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

von Angerer, S. "Reaction of Azetidinones with Imidates." In Science of Synthesis Knowledge Updates KU 2011/1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-116-00254.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Boyd, G. V. "From an Azetidinone." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00621.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Mahapatra, Monalisa, Kakarla Pakeeraiah, Suman Kumar Mekap, and Sudhir Kumar Paidesetty. "AZETIDINONE DERIVED DRUGS: BIOLOGICAL SIGNIFICANCE AND THEIR FUTURE SCOPE IN CHEMICAL SYNTHESIS." In Futuristic Trends in Chemical Material Sciences & Nano Technology Volume 3 Book 19. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bacs19p1ch2.

Full text
Abstract:
Drug discovery and chemical synthesis have been globalizing the pharmaceutical market. The process of drug discovery takes along many stages of drug development viz., targeting a disease, repurposing an existing drug, conjugating obsolete drugs with natural compounds, searching for different receptors for specificity and rationality, and finally testing the toxicity before exposing it tothe clinical trial. This long path from targeting to clinical trial takes many efforts of scientists and chemists. When entering into the drug development core, the heterocyclic compounds were ruling the world by their swiftness in reaction mechanism and displaying good pharmacological activity. Focusing on the heterocyclic compounds, β-lactam is a well-known pharmacophore being accepted for many existing drugs viz., Penicillin, cefixime, cefalixine, and other derivatives of penicillin. The congeners of 2-azetidine were also known to possess numerous biological actions viz., antitubercular, anti-inflammatory, anticancer, antidiabetic, antipsychotic, anti-inflammatory,and vasopressin via antagonist activities
APA, Harvard, Vancouver, ISO, and other styles
9

Pramod, N., C. Bharath Kumar, P. Sri Lekha, and B. Mayuri. "Role of Pyridine Containing Azetidinone Derivatives as Privileged Scaffolds in Anti Tubercular Agents." In Technological Innovation in Pharmaceutical Research Vol. 11. Book Publisher International (a part of SCIENCEDOMAIN International), 2021. http://dx.doi.org/10.9734/bpi/tipr/v11/3921f.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Taber, Douglass F. "C-N Ring Construction: The Synthesis of Decursivine by Mascal and by Jia." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0056.

Full text
Abstract:
Barry M. Trost and Justin Du Bois of Stanford University described (Org. Lett. 2011, 13, 3336) the cyclization of 1 to the activated aziridine 2. Liming Zhang of the University of California, Santa Barbara, rearranged (Angew. Chem. Int. Ed. 2011, 50, 3236) the propergylic amine 3 to the azetidinone 4 by N-H insertion of an intermediate Au carbene. Xiao Zheng and Pei-Qiang Huang of Xiamen University effected (J. Org. Chem. 2011, 76, 4952) reductive coupling of 6 with 7 to deliver the ester 8 . Eiji Tayama of Niigata University found (Tetrahedron Lett. 2011, 52, 1819) that 9 could be alkenylated with 10 with substantial retention of absolute configuration. Duncan J. Wardrop of the University of Illinois at Chicago, en route to a synthesis of (-)-swainsonine, observed (Org. Lett. 2011 , 13, 2376) high diastereocontrol in the cyclization of 12 to 13. Iain Coldham of the University of Sheffield also observed (J. Org. Chem. 2011, 76, 2360) substantial diastereoselection in the cyclization of 14 to 15. Robert E. Gawley of the University of Arkansas established (Org. Lett. 2011, 13, 394) that exposure of metalated 16 to just 5 mol % of a chiral ligand was sufficient to enable enantioselective coupling, to deliver 17. Christian Nadeau of Merck Frosst effected (J. Am. Chem. Soc. 2011, 133, 2878) enantioselective addition to the pyridinium salt 19 to give 20. Jiyong Hong of Duke University observed (Org. Lett. 2011, 13, 796) that enantiomerically pure 21 cyclized to the cis diastereomer of 22. With the Hayashi catalyst, cyclization could be driven toward the trans diastereomer, 22, enabling the synthesis of (+)-myrtine. Dawei Ma of the Shanghai Institute of Organic Chemistry found (Org. Lett. 2011, 13, 1602) that the Hayashi catalyst also directed the relative and absolute outcome in the addition of 24 to 23 , to give the piperidine 25. Donn G. Wishka of Pfizer/Groton devised (J. Org. Chem. 2011, 76, 1937) a practical route to the cis-substituted azepane 27, by Beckmann rearrangement of the enantiomerically pure 26 followed by reduction and oxidative cleavage.
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Azetidinones"

1

Kadhim, Amani Nadhim, Zeid Hassan Abood, Husham Attallah Suhail, and Sarah Salah Jalal. "Antibacterial actions of some new easy azetidinone derivatives." In PHYSICAL MESOMECHANICS OF CONDENSED MATTER: Physical Principles of Multiscale Structure Formation and the Mechanisms of Nonlinear Behavior: MESO2022. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0157221.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Hassan, Hammed H. A. M., and Raafat Soliman. "DI-ALPHA-N-(2'-AZETIDINONE)-2-AZETIDINONE HAVING N-SULFONAMIDE DRUGS SIDE CHAIN: A NEW TYPE OF BETA-LACTAMS CONTAINING CARBOHYDRATES." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.636.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Sankar, P. Siva, K. Divya, G. Dinneswara Reddy, V. Padmavathi, and Grigory V. Zyryanov. "Synthesis, characterization and antimicrobial activity of azetidinone and thiazolidinone derivatives." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087379.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Luna, Amparo, Pedro Almendros, and Benito Alcaide. "Diastereoselective direct aldol reaction and subsequent cyclization of 2-azetidinone-tethered azides for the preparation of a 4-hydroxypipecolic acid analogue." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00174.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Azetidinones' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography