Collect. Czech. Chem. Commun.
1990, 55, 524-534
https://doi.org/10.1135/cccc19900524
Nitriles in heterocyclic synthesis: A novel route for the synthesis of naphthodipyrans, pyridines. 2H- and 4H-Pyrans
Abdel Ghani A. Elagameya, Fathy M. A. El-Taweela, Salah Z. A. Sowellima, Mamdouh A. Sofana and Mohamed H. Elnagdib
a Chemistry Department, Mansoura University, Damietta, Egypt
b Chemistry Department, Cairo University, Cairo, Egypt
Crossref Cited-by Linking
- Rajabi‐salek Mostafa, Zolfigol Mohammad Ali, Zarei Mahmoud, Noroozizadeh Ehsan, Mohammadpoor‐Baltork Iraj, Rudbari Hadi Amiri: Synthesis and Characterization of 1‐(Carboxymethyl)Pyridinium Bromide [CMPy]Br Molten Salt: Application as a Novel Nanocatalyst for the Synthesis of Bis‐Naphthodipyrans. ChemistrySelect 2018, 3, 12791. <https://doi.org/10.1002/slct.201802971>
- Rosati Ornelio, Lanari Daniela, Scavo Raffaella, Persia Diana, Marmottini Fabio, Nocchetti Morena, Curini Massimo, Piermatti Oriana: Zirconium potassium phosphate methyl and/or phenyl phosphonates as heterogeneous catalysts for Knoevenagel condensation under solvent free conditions. Microporous and Mesoporous Materials 2018, 268, 251. <https://doi.org/10.1016/j.micromeso.2018.04.035>
- Khazaei Ardeshir, Bashirian Ehsan, Ranjbaran Azam, Khazaei Marzieh, Moosavi‐Zare Ahmad Reza: The Synthesis of 2,11‐Diamino‐4,9‐diphenyl‐4,9‐dihydrobenzo [f] pyrano[3,2‐h]chromene‐3,10‐dicarbonitrile Derivatives using Triethanolammonium Acetate as a Green Ionic Liquid. J Chinese Chemical Soc 2017, 64, 757. <https://doi.org/10.1002/jccs.201700019>
- Salama Soad K., Darweesh Ahmed F., Abdelhamid Ismail A., Elwahy Ahmed H. M.: Microwave Assisted Green Multicomponent Synthesis of Novel bis(2‐Amino‐tetrahydro‐4H‐chromene‐3‐carbonitrile) Derivatives Using Chitosan as Eco‐friendly Basic Catalyst. Journal of Heterocyclic Chem 2017, 54, 305. <https://doi.org/10.1002/jhet.2584>
- Bardasov Ivan N., Alekseeva Anastasiya U., Mihailov Denis L., Ershov Oleg V., Grishanov Dmitry A.: Double heteroannulation reactions of 1-naphthol with alkyl- and arylmethylidene derivatives of malononitrile dimer. Tetrahedron Letters 2015, 56, 1830. <https://doi.org/10.1016/j.tetlet.2015.02.081>
- Osipov D. V., Osyanin V. A., Klimochkin Yu. N.: New synthesis of 3-amino-1H-benzo[f]chromene-2-carbonitriles. Russ J Org Chem 2013, 49, 398. <https://doi.org/10.1134/S1070428013030147>
- Khalil Khaled, Al-Matar Hamad: Chitosan Based Heterogeneous Catalyses: Chitosan-Grafted-Poly(4-Vinylpyridne) as an Efficient Catalyst for Michael Additions and Alkylpyridazinyl Carbonitrile Oxidation. Molecules 2013, 18, 5288. <https://doi.org/10.3390/molecules18055288>
- Abd El-Wahab Ashraf H. F.: Synthesis, Reactions and Evaluation of the Antimicrobial Activity of Some 4-(p-Halophenyl)-4H-naphthopyran, Pyranopyrimidine and Pyranotriazolopyrimidine Derivatives. Pharmaceuticals 2012, 5, 745. <https://doi.org/10.3390/ph5070745>
- Mahmoud Alaa F., Abd El‐Latif Fathy F., Ahmed Amira M.: Microwave Assisted One‐pot Synthesis of 2‐Amino‐4H‐chromenes and Spiropyrano[2,3‐d]pyrimidine. Chin. J. Chem. 2010, 28, 91. <https://doi.org/10.1002/cjoc.201090041>
- Behbehani Haider, Mohamed Ibrahim Hamada, Makhseed Saad: Studies with 3-Oxoalkanonitriles: Synthesis and Reactivity of 3-Oxo-3-(1-methylindoloyl)propanenitrile. HETEROCYCLES 2009, 78, 3081. <https://doi.org/10.3987/COM-09-11818>
- Balalaie Saeed, Ramezanpour Sorour, Bararjanian Morteza, Gross Jürgen H.: DABCO‐Catalyzed Efficient Synthesis of Naphthopyran Derivatives via One‐Pot Three‐Component Condensation Reaction at Room Temperature. Synthetic Communications 2008, 38, 1078. <https://doi.org/10.1080/00397910701862865>
- Khafagy Mostafa M, Abd El-Wahab Ashraf H.F, Eid Fathy A, El-Agrody Ahmed M: Synthesis of halogen derivatives of benzo[h]chromene and benzo[a]anthracene with promising antimicrobial activities. Il Farmaco 2002, 57, 715. <https://doi.org/10.1016/S0014-827X(02)01263-6>
- Sharanin Yu A, Goncharenko M P, Litvinov Victor P: Reactions of carbonyl compounds with α,β-unsaturated nitriles as a convenient pathway to carbo- and heterocycles. Russ. Chem. Rev. 1998, 67, 393. <https://doi.org/10.1070/RC1998v067n05ABEH000371>
- Erian Ayman Wahba, Elkholy Yehya Mahmoud, Al-arab Elham Ezz, Elnagdf Mohamed Hilmy: POLYFUNCTIONALLY SUBSTITUTED HETEROCYCLES: SYNTHESIS OF NEW POLYFUNCTIONALLY SUBSTITUTED PHTHALAZINES, PYRIDO[3,4-C]PYRIDAZINES AND PYRAZOLO[3,4-C]PYRIDAZINES. Phosphorus, Sulfur, and Silicon and the Related Elements 1997, 122, 133. <https://doi.org/10.1080/10426509708043501>
- Sadek Kamal Usef, Selim Maghraby Ali, Ali Mohamed, Elnagdi Mohamed Hilmy: Nitriles in heterocyclic synthesis: The reaction of ethyl 2‐oxoindoliden‐3‐ylidene cyanoacetate and of 3‐dicyanoethylideneindoliden‐2‐one with phenols and amines. Heteroatom Chemistry 1995, 6, 597. <https://doi.org/10.1002/hc.520060618>
- El-Taweel Fathy Mohamed Abdel Aziz, Sowellim Salah Zaki Ahmed, Elagamey Abdel Ghani Ali: Reactions with 2(1H)-Quinolinone and Coumarine Derivatives: New Routes to Polysubstituted 2(1H)-Quinolinone and Coumarine Derivatives. Bulletin of the Chemical Society of Japan 1995, 68, 905. <https://doi.org/10.1246/bcsj.68.905>
- Kotali Antigoni, Harris Philip A.: o-HYDROXYARYL KETONES IN ORGANIC SYNTHESIS. A REVIEW. Organic Preparations and Procedures International 1994, 26, 159. <https://doi.org/10.1080/00304949409458025>
- Elagamey Abdel Ghani Ali, El-Taweel Fathy Mohamed Abdel-Aziz, Khodeir Mohamed Nabil Mohamed, Elnagdi Mohamed Hilmy: Nitriles in Heterocyclic Synthesis. The Reaction of Polyhydric Naphthalenes, 4-Methylcoumarin-3-carbonitrile, and Alkylidenemalononitrile with Methylenemalononitrile. Bulletin of the Chemical Society of Japan 1993, 66, 464. <https://doi.org/10.1246/bcsj.66.464>
- Hafez Ali A. Abdel, Awad Ibrahim M. A., Monem Maisa I. Abdel: Nitriles in heterocyclic synthesis. Part III: New sulpha drugs related to cyanopyridine derivatives. J of Chemical Tech & Biotech 1992, 55, 333. <https://doi.org/10.1002/jctb.280550405>
- ELAGAMEY A. G. A., EL‐TAWEEL F. M. A., SOWELLIM S. Z. A., SOFAN M. A., ELNAGDI M. H.: ChemInform Abstract: Nitriles in Heterocyclic Synthesis: A Novel Route for the Synthesis of Naphthodipyrans, Pyridines. 2H‐ and 4H‐Pyrans. ChemInform 1990, 21. <https://doi.org/10.1002/chin.199024159>