Relevant bibliographies by topics / Erlenmeyer Azlactone Synthesis / Journal articles
To see the other types of publications on this topic, follow the link: Erlenmeyer Azlactone Synthesis.

Journal articles on the topic 'Erlenmeyer Azlactone Synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

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

Select a source type:

Consult the top 24 journal articles for your research on the topic 'Erlenmeyer Azlactone Synthesis.'

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.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Karade, N. N., S. G. Shirodkar, B. M. Dhoot, and P. B. Waghmare. "Montmorillonite K-10 mediated Erlenmeyer synthesis of 4-arylmethylene-2-phenyl-5(4H)-oxazolones." Journal of Chemical Research 2005, no. 1 (January 2005): 46–47. http://dx.doi.org/10.3184/0308234053431176.

Full text
Abstract:
Aromatic aldehydes and hippuric acid in acetic anhydride undergoes classical Erlenmeyer synthesis in the presence of a catalytic amount of Montmorillonite K-10 to afford the corresponding azlactones in excellent yields with high selectivity. The azlactone formation does not proceed in the absence of either acetic anhydride or Montmorillonite.
APA, Harvard, Vancouver, ISO, and other styles
2

Shafiee, Behnaz, Laleh Hadian, and Ahmad R. Khosropour. "An innovation for development of Erlenmeyer–Plöchl reaction and synthesis of AT-130 analogous: a new application of continuous-flow method." RSC Advances 6, no. 24 (2016): 19861–66. http://dx.doi.org/10.1039/c6ra00301j.

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

Chandrasekhar, Sosale, and Phaneendrasai Karri. "Aromaticity in azlactone anions and its significance for the Erlenmeyer synthesis." Tetrahedron Letters 47, no. 32 (August 2006): 5763–66. http://dx.doi.org/10.1016/j.tetlet.2006.06.006.

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

Chandrasekhar, Sosale, and Phaneendrasai Karri. "Erlenmeyer azlactone synthesis with aliphatic aldehydes under solvent-free microwave conditions." Tetrahedron Letters 48, no. 5 (January 2007): 785–86. http://dx.doi.org/10.1016/j.tetlet.2006.11.174.

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

Verma, Tarawanti, Manish Sinha, and Nitin Bansal. "Synthesis of Novel 1,2-Dihydro-1,2,4-Triazin-6(5H)-one Derivatives as Anticancer Agents." Current Bioactive Compounds 16, no. 7 (October 28, 2020): 1116–31. http://dx.doi.org/10.2174/1573407215666191022123310.

Full text
Abstract:
Introduction: Cancer is still an untreatable disease and the second leading cause of death globally. The heterocyclic compounds have always played a major role in the anticancer drug discovery program. 1,2,4-Triazine-6-ones is a heterocyclic privileged structure with diversified activities. In the presented study, 21 novel 2,5-disubstituted-3-phenyl-1,2-dihydro-1,2,4-triazin-6 (5H)-one derivatives (13(a-k), 18(a-j) and 21(a1-a4, b)) have been synthesized and tested for their anticancer activity. Methods: The 2,5-disubstituted-3-phenyl-1,2-dihydro-1,2,4-triazin-6(5H)-one derivatives (13(a-k), 18(a-j) and 21(a1-a4, b) were synthesized by refluxing substituted-2-phenyloxazol-5(4H)-one and hydrazine derivatives. Substituted aldehydes were synthesized via Vilsmeier-Haack reaction, while substituted- 2-phenyloxazol-5(4H)-one derivatives were synthesized by Erlenmeyer Plochl azlactone synthesis. Twenty-one compounds were selected and screened at the National Cancer Institute (NCI), USA, for anticancer activity at a single high dose (10-5M) in full NCI 60 cell panel assay. Results and Conclusion: The selected compounds (13a, 13b, 13c, 13f, 13h, 13i, 13j, 18h, 18i, 21a4) were found to be active against different cancer cell lines. The compound, 5-((5-chloro-3-methyl-1- phenyl-1H-pyrazol-4-yl)methylene)-2-(4-nitrobenzoyl)-3-phenyl-1,2-dihydro-1,2,4-triazin-6(5H)-one (13a) was found to be a potent anti-cancer agent as electron-rich moiety on phenyl at position 2 of triazine nucleus, having a great impact on anticancer activity.
APA, Harvard, Vancouver, ISO, and other styles
6

Parveen, Mehtab, Faheem Ahmad, Ali Mohammed Malla, Shaista Azaz, Manuela Ramos Silva, and P. S. Pereira Silva. "[Et3NH][HSO4]-mediated functionalization of hippuric acid: an unprecedented approach to 4-arylidene-2-phenyl-5(4H)-oxazolones." RSC Advances 5, no. 65 (2015): 52330–46. http://dx.doi.org/10.1039/c5ra09290f.

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

Jagadale, Megha, Altafhusen Naikwade, Rajashri Salunkhe, Mohan Rajmane, and Gajanan Rashinkar. "An ionic liquid gel: a heterogeneous catalyst for Erlenmeyer–Plochl and Henry reactions." New Journal of Chemistry 42, no. 13 (2018): 10993–1005. http://dx.doi.org/10.1039/c8nj00367j.

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

Zhou, Baocheng, and Wenxing Chen. "The Zwitterionic Imidazolium Salt: First Used for Synthesis of 4-Arylidene-2-phenyl-5(4H)-oxazolones under Solvent-Free Conditions." Journal of Chemistry 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/280585.

Full text
Abstract:
The zwitterionic imidazolium salt was prepared and characterized by1H NMR. It was first used for synthesis of azlactones via Erlenmeyer synthesis from aromatic aldehydes and hippuric acid under solvent-free conditions. It was found that aldehyde substituents play an important role in these reactions. Better conversions and therefore higher isolated yields were observed when electron-withdrawing groups (EWG-) were present in the aromatic aldehyde. Opposite results were shown when electron-donating groups (EDG-) were present in the aromatic aldehyde. However, azlactones were obtained in moderate to high yields.
APA, Harvard, Vancouver, ISO, and other styles
9

El-Mekabaty, Ahmed. "ChemInform Abstract: Erlenmeyer Azlactones. Synthesis, Reactions and Biological Activity." ChemInform 44, no. 34 (August 1, 2013): no. http://dx.doi.org/10.1002/chin.201334216.

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

Kiyani, Hamzeh, and Shiva Aslanpour. "Synthesis of Erlenmeyer-Plöchl Azlactones Promoted by 5-Sulfosalicylic Acid." HETEROCYCLES 94, no. 7 (2017): 1314. http://dx.doi.org/10.3987/com-17-13711.

Full text
APA, Harvard, Vancouver, ISO, and other styles
11

Conway, Philip A., Kevin Devine, and Francesca Paradisi. "A simple and efficient method for the synthesis of Erlenmeyer azlactones." Tetrahedron 65, no. 15 (April 2009): 2935–38. http://dx.doi.org/10.1016/j.tet.2009.02.011.

Full text
APA, Harvard, Vancouver, ISO, and other styles
12

Parveen, Mehtab, Akhtar Ali, Sarfaraz Ahmed, Ali Mohammed Malla, Mahboob Alam, P. S. Pereira Silva, Manuela Ramos Silva, and Dong-Ung Lee. "Synthesis, bioassay, crystal structure and ab initio studies of Erlenmeyer azlactones." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 104 (March 2013): 538–45. http://dx.doi.org/10.1016/j.saa.2012.11.054.

Full text
APA, Harvard, Vancouver, ISO, and other styles
13

Rostamizadeh, Nader, Alireza Khajeh-Amiri, and Hassan Moghanian. "Microwave-Assisted Erlenmeyer Synthesis of Azlactones Catalyzed by MgO/Al2O3Under Solvent-Free Conditions." Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry 46, no. 5 (December 15, 2015): 631–34. http://dx.doi.org/10.1080/15533174.2014.989575.

Full text
APA, Harvard, Vancouver, ISO, and other styles
14

Yu, Chuanming, Baocheng Zhou, Weike Su, and Zhenyuan Xu. "Erlenmeyer Synthesis for Azlactones Catalyzed by Ytterbium(III) Triflate under Solvent‐Free Conditions." Synthetic Communications 36, no. 22 (November 1, 2006): 3447–53. http://dx.doi.org/10.1080/00397910600941521.

Full text
APA, Harvard, Vancouver, ISO, and other styles
15

Monk, Keith A., Dusan Sarapa, and Ram S. Mohan. "Bismuth (III) Acetate: A New Catalyst for Preparation of Azlactones via the Erlenmeyer Synthesis." Synthetic Communications 30, no. 17 (September 2000): 3167–70. http://dx.doi.org/10.1080/00397910008086926.

Full text
APA, Harvard, Vancouver, ISO, and other styles
16

Monk, Keith A., Dusan Sarapa, and Ram S. Mohan. "ChemInform Abstract: Bismuth(III) Acetate: A New Catalyst for Preparation of Azlactones via the Erlenmeyer Synthesis." ChemInform 31, no. 44 (October 31, 2000): no. http://dx.doi.org/10.1002/chin.200044138.

Full text
APA, Harvard, Vancouver, ISO, and other styles
17

Fadavi, Abdulhamid, and Maaroof Zarei. "One-pot Vilsmeier reagent-mediated multicomponent reaction: A direct synthesis of oxazolones and Erlenmeyer azlactones from carboxylic acids." Comptes Rendus Chimie 21, no. 1 (January 2018): 9–13. http://dx.doi.org/10.1016/j.crci.2017.12.001.

Full text
APA, Harvard, Vancouver, ISO, and other styles
18

Kiyani, Hamzeh, and Shiva Aslanpour. "Correction to “Synthesis of Erlenmeyer-Plöchl Azlactones Promoted by 5-Sulfosalicylic Acid”: HETEROCYCLES, 2017, 94, 1314, DOI: 10.3987/COM-17-13711." HETEROCYCLES 98, no. 4 (2019): 619. http://dx.doi.org/10.3987/correction-com-17-13711.

Full text
APA, Harvard, Vancouver, ISO, and other styles
19

Chandrasekhar, Sosale, and Phaneendrasai Karri. "Erlenmeyer Azlactone Synthesis with Aliphatic Aldehydes under Solvent-Free Microwave Conditions." ChemInform 38, no. 17 (April 24, 2007). http://dx.doi.org/10.1002/chin.200717119.

Full text
APA, Harvard, Vancouver, ISO, and other styles
20

Mogilaiah, K., M. Prashanthi, and Ch Srinivas Reddy. "Solid Support Erlenmeyer Synthesis of Azlactones (III) Using Microwaves." ChemInform 34, no. 52 (December 30, 2003). http://dx.doi.org/10.1002/chin.200352130.

Full text
APA, Harvard, Vancouver, ISO, and other styles
21

Conway, Philip A., Kevin Devine, and Francesca Paradisi. "ChemInform Abstract: A Simple and Efficient Method for the Synthesis of Erlenmeyer Azlactones." ChemInform 40, no. 33 (August 18, 2009). http://dx.doi.org/10.1002/chin.200933133.

Full text
APA, Harvard, Vancouver, ISO, and other styles
22

Yu, Chuanming, Baocheng Zhou, Weike Su, and Zhenyuan Xu. "Erlenmeyer Synthesis for Azlactones Catalyzed by Ytterbium(III) Triflate under Solvent-Free Conditions." ChemInform 38, no. 16 (April 17, 2007). http://dx.doi.org/10.1002/chin.200716120.

Full text
APA, Harvard, Vancouver, ISO, and other styles
23

Anil, Seegehalli M., Muddenahalli S. Sudhanva, Toreshettahally R. Swaroop, Ajjampura C. Vinayaka, Narasimhamurthy Rajeev, Kuppalli R. Kiran, Rangappa Shobith, and Maralinganadoddi P. Sadashiva. "Base Induced Condensation of Malononitrile with Erlenmeyer Azlactones: An Unexpected Synthesis of Multi‐Substituted Δ 2 ‐Pyrrolines and Their Cytotoxicity." Chemistry & Biodiversity 17, no. 5 (April 16, 2020). http://dx.doi.org/10.1002/cbdv.202000014.

Full text
APA, Harvard, Vancouver, ISO, and other styles
24

Shinde, Rameshwar S., Aditya R. Narnawre, Prashik M. Walke, and Nandkishor N. Karade. "(Diacetoxyiodo)benzene Mediated Oxidative Conversion of Erlenmeyer Azlactones to 2‐Substituted Oxazolines Under Basic Conditions: Synthesis of 4‐Methoxy‐2‐phenyl‐5‐aryl‐4,5‐dihydrooxazole‐4‐carboxylate." ChemistrySelect 8, no. 1 (January 2, 2023). http://dx.doi.org/10.1002/slct.202203899.

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