Academic literature on the topic 'Chroman derivatives synthesis'

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Journal articles on the topic "Chroman derivatives synthesis"

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Matta, Akanksha, Ajendra K. Sharma, Shilpi Tomar, et al. "Synthesis and anti-inflammatory activity evaluation of novel chroman derivatives." New Journal of Chemistry 44, no. 32 (2020): 13716–27. http://dx.doi.org/10.1039/d0nj02125c.

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In an effort to develop potent anti-inflammatory agents, a series of novel chroman derivatives including acyclic amidochromans, chromanyl esters and chromanyl acrylates have been designed, synthesized and fully characterized.
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Jakkampudi, Satish, Ramarao Parella, and John C. G. Zhao. "Stereoselective synthesis of chromane derivatives via a domino reaction catalyzed by modularly designed organocatalysts." Organic & Biomolecular Chemistry 17, no. 1 (2019): 151–55. http://dx.doi.org/10.1039/c8ob02677g.

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Lv, Xue-Jiao, Wei-Wei Zhao, Ying-Han Chen, Sheng-Biao Wan, and Yan-Kai Liu. "Organocatalytic asymmetric synthesis of both cis- and trans-configured pyrano[2,3-b]chromenes via different dehydration pathways." Organic Chemistry Frontiers 6, no. 12 (2019): 1972–76. http://dx.doi.org/10.1039/c9qo00366e.

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Tangeti, Venkata S., Kattaru R. Babu, Dasari Vasundhara, K. V. V. V. Satyanarayana, Himabindu Mylapalli, and Kaja S. P. Kumar. "One Pot Synthesis of Novel Substituted 2',4'-Dihydrospiro[chroman-2,3'-pyrazol]-4- one Derivatives." Current Organic Synthesis 15, no. 2 (2018): 267–74. http://dx.doi.org/10.2174/1570179414666171011161836.

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Aim and Objective: In the work, we have successfully presented a synthetic route for the synthesis of novel 2',4'-dihydrospiro[chroman-2,3'-pyrazol]-4-one derivatives via one pot multicomponent approach. Materials and Method: Substituted 2',4'-dihydrospiro[chroman-2,3'-pyrazol]-4-one were prepared through cascade three-component condensation of ortho-hydroxyacetophenone, β-ketoester, hydrazine in the presence of pyrrolidine as a catalyst under ethanol reflux conditions. Results: A series of novel 2',4'-dihydrospiro[chroman-2,3'-pyrazol]-4-one have been synthesized through a facile strategy. Th
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Geng, Zhi-Cong, Shao-Yun Zhang, Nai-Kai Li, et al. "Organocatalytic Diversity-Oriented Asymmetric Synthesis of Tricyclic Chroman Derivatives." Journal of Organic Chemistry 79, no. 22 (2014): 10772–85. http://dx.doi.org/10.1021/jo501560m.

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Hashmi, A. Stephen K, Matthias Rudolph, Jan W Bats, Wolfgang Frey, Frank Rominger, and Thomas Oeser. "Gold-Catalyzed Synthesis of Chroman, Dihydrobenzofuran, Dihydroindole, and Tetrahydroquinoline Derivatives." Chemistry - A European Journal 14, no. 22 (2008): 6672–78. http://dx.doi.org/10.1002/chem.200800210.

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Subba Reddy, B. V., V. Hanuman Reddy, Durgaprasad Medaboina, B. Sridhar, and Y. V. Rami Reddy. "A tandem Prins spirocyclization for the stereoselective synthesis of tetrahydrospiro[chroman-2,4′-pyran] derivatives." Organic & Biomolecular Chemistry 14, no. 12 (2016): 3234–37. http://dx.doi.org/10.1039/c5ob02639c.

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A novel cascade process has been developed for the synthesis of tetrahydrospiro[chroman-2,4′-pyran] derivatives by condensation of aldehydes with 2-(5-hydroxy-3-methylenepentyl)phenols using BF<sub>3</sub>·OEt<sub>2</sub> under mild reaction conditions.
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Li, Jun-Hua, and Da-Ming Du. "Correction: Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide." Organic & Biomolecular Chemistry 13, no. 26 (2015): 7337. http://dx.doi.org/10.1039/c5ob90099a.

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Correction for ‘Enantioselective synthesis of chiral heterocycles containing both chroman and pyrazolone derivatives catalysed by a chiral squaramide’ by Jun-Hua Li, et al., Org. Biomol. Chem., 2015, 13, 5636–5645.
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Y. Raoof, Moneera. "Synthesis of some Thiadiazoline Derivatives from 2- Phenyl Chroman-4-one." Rafidain Journal of Science 24, no. 9 (2013): 32–41. http://dx.doi.org/10.33899/rjs.2013.78757.

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Geng, Zhi-Cong, Shao-Yun Zhang, Nai-Kai Li, et al. "ChemInform Abstract: Organocatalytic Diversity-Oriented Asymmetric Synthesis of Tricyclic Chroman Derivatives." ChemInform 46, no. 18 (2015): no. http://dx.doi.org/10.1002/chin.201518173.

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Dissertations / Theses on the topic "Chroman derivatives synthesis"

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Shervington, L. A. "Studies on a new synthesis of chromans." Thesis, Bucks New University, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.380298.

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Nocanda, Xolani Wittleton. "Applications of Baylis-Idllman methodology in the synthesis of chromene derivatives." Thesis, Rhodes University, 2001. http://hdl.handle.net/10962/d1018257.

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The reaction of salicylaldehyde with various activated alkenes, viz., methyl vinyl ketone, ethyl vinyl ketone, phenyl vinyl sulfone, phenyl vinylsulfonate, acrolein and acrylonitrile, under Baylis-Hillman conditions, has been found to proceed with the chemoselective formation of chromene derivatives. The reaction conditions have been optimised and chromene derivatives have been obtained in isolated yields up to 87 %. The generality of the reaction, using 1,4-diazabicyclo[2.2.2]octane (DABCO), as the catalyst, and a heterogeneous (chloroform-water) solvent system, has been established using a r
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Ramaite, Ipfani David Isaiah. "Synthetic and physical organic studies of chromone derivatives." Thesis, Rhodes University, 1997. http://hdl.handle.net/10962/d1005045.

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A range of chromone-2-carboxylic acids has been prepared by condensing suitably substituted 2-hydroxyacetophenones with diethyl oxalate. pK₂ Studies of these acids revealed that 6- or 7-methoxy substituents decreased acidity while the 6-nitro group enhanced acidity; the strongest acid was the 3-chloro derivative, the increase in acidity being attributed to steric inhibition of acid-weakening delocalisation between the carboxyl group and the chromone system. Various chromone-2-carboxamides, derived from acid chloride precursors, were converted to polysubstituted acrylamides by nucleophilic ring
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Molefe, Duduzile Mabel. "Studies directed towards the synthesis of chromone carbaldehyde-derived HIV-1 protease inhibitors." Thesis, Rhodes University, 2008. http://hdl.handle.net/10962/d1015542.

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A series of chromone-3-carbaldehydes have been prepared using Vilsmeier-Haack methodology while a corresponding series of chromone-2-carbaldeydes have been synthesized via the Kostanecki-Robinson reaction. Baylis-Hillman reactions have been conducted on both series of chromone carbaldehydes using three different catalysts, viz., 1,4-diazabicyclo(2.2.2]octane (DABCO), 1,8-diazabicyclo[5.4.0]undec- 7-ene (DBU) and 3-hydroxyquinuclidine (3HQ), and acrylonitrile, methyl acrylate and methyl vinyl ketone as the activated alkenes. These reactions have typically (but not always!) afforded both normal
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Huang, Chia-Yu, and 黃傢裕. "Synthesis of Indole, Indoline, Benzofuran and Chroman Derivatives from Nitroalkenes." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/79382536634409889369.

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碩士<br>國立臺灣師範大學<br>化學系<br>103<br>The contents of the thesis is divided into two chapters, each chapter individually including preface, research goal, result and discussion, and conclusion. Chapter I deals with the copper-catalyzed Ullmann reaction to synthesize 3-arylindoles, in which the precursors are furnished by AlCl3-catalyzed Friedel-Crafts alkylation of beta-nitrostyrenes and arenes followed by reduction. Chapter II discuss about the applicability of beta-nitrostyrene derivatives for the synthesis of structurally three types of compounds. The chapter is divided into three parts, first pa
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YANG, YA-AN, and 楊雅安. "Part I、Synthesis of Coumarin-fused Pyrido[2,1-a]isoquinolin-8-ium Heterocycles and Their DerivativesPart II、Multicomponent Synthesis of (3E)-3-[Alkylamino(aryl)methylidene]chroman-2,4-diones and -Nitro Amide Derivatives." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/z6e558.

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碩士<br>東海大學<br>化學系<br>106<br>Part I、Synthesis of Coumarin-fused Pyrido[2,1-a]isoquinolin -8-ium Heterocycles and Their Derivatives Protoberberines are alkaloids that exhibit a wide range of biological activities such as antimicrobial, anti-inflammatory, antimalarial, and antitumor. Previous synthetic efforts have been primarily focused on the biological and therapeutic applications of protoberberines, their intrinsic photochemical properties were much less explored. In this study, a coumarin and pyrido[2,1-a]isoquinolin-8-ium-fused heterocycles were synthesized by p-TsOH-mediated coupling
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Chang, Ho-Chiang, and 張豪晉. "1. Synthesis of Substituted 1-Benzoxepin-2-one from Isovanillin via Ring-Closing Metathesis (RCM)2. A New Approach for the Synthesis of Mellein Derivatives from Isovanillin via 3,4-Dihydro-2-chroman Intermediate." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/88918019211283716041.

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碩士<br>高雄醫學大學<br>醫藥暨應用化學研究所<br>98<br>Part I Isovanillin was used as starting material which underwent sequential reactions such as O-alkylation, and ring-closing metathesis (RCM) to provide substituted 1-benzoxepin-2-one derivatives. Part II Utilization of O-alkylation, Claisen rearrangement, reduction, oxymercuration-demercuration and oxidation in sequences, a series of mellein derivatives were synthesized via 3,4-dihydro-2-chroman intermediate from isovanillin.
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Gonçalves, Ana Alexandra Gomes. "Synthesis of chromene derivatives with potential anticancer activity." Master's thesis, 2013. http://hdl.handle.net/1822/28328.

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Dissertação de mestrado em Química Medicinal<br>Colorectal carcinoma (CRC) is the second leading cause of cancer-related death in industrialized countries and the search for new therapeutic approaches is of prime importance. Chromene-based compounds are present in many natural products and their interest in organic chemistry is mainly due to the multiple biological properties. In this work, several chromene derivatives were synthesized using simple and environmentally benign approaches, and were tested in vitro against human cancer cell lines HCT116, HT29 and RKO. The first part of this
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Li, Da-Fang, and 李達方. "A new method for the synthesis of chromene derivatives." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/68874984114167477458.

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碩士<br>高雄醫學大學<br>醫藥暨應用化學研究所碩士在職專班<br>96<br>A new route to the synthesis of chromene derivatives from resorcinol is studied.The synthetic rout involues Wittg reaction, alkylation, ring-closing metathesis (RCM) and Claisen rearrangement. The final products have the similar skeleton to osthol structure. In the new synthetic approach, the chromene derivatives prepare from the resorcinol that was reacted with acetyl chloride, benzyl bromide, allyl bromide and methoxyacetophenone. Then, the diene compounds were reacted with Grubb’2nd catalyst via ring-closing metathesis (RCM).
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Ramonetha, Thata Golden. "Synthetic and spectroscopic studies of 6-substituted chromone derivatives." Diss., 2015. http://hdl.handle.net/11602/772.

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Book chapters on the topic "Chroman derivatives synthesis"

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Taber, Douglass F. "Substituted Benzenes: The Reddy Synthesis of Isofregenedadiol." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0062.

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Jianbo Wang of Peking University (Org. Lett. 2011, 13, 4988) and Patrick Y. Toullec and Véronique Michelet of Chimie ParisTech (Org. Lett. 2011, 13, 6086) developed conditions for the electrophilic acetoxylation of a benzene derivative 1. Seung Hwan Cho and Sukbok Chang of KAIST (J. Am. Chem. Soc. 2011, 133, 16382) and Brenton DeBoef of the University of Rhode Island (J. Am. Chem. Soc. 2011, 133, 19960) devised protocols for the electrophilic imidation of a benzene derivative 3. Vladimir V. Grushin of ICIQ Tarragona devised (J. Am. Chem. Soc. 2011, 133, 10999) a simple protocol for the cyanation of a bromobenzene 6 to the nitrile 7. Hua-Jian Xu of the Hefei University of Technology (J. Org. Chem. 2011, 76, 8036) and Myung-Jong Jin of Inha University (Org. Lett. 2011, 13, 5540) established conditions for the efficient Heck coupling of a chlorobenzene 8. Jacqueline E. Milne of Amgen/Thousand Oaks reduced (J. Org. Chem. 2011, 76, 9519) the adduct from the addition of 11 to 12 to deliver the phenylacetic acid 13. Jeffrey W. Bode of ETH Zurich effected (Angew. Chem. Int. Ed. 2011, 50, 10913) Friedel-Crafts alkylation of 14 with the hydroxamate 15 to give the meta product 16. B.V. Subba Reddy of the Indian Institute of Chemical Technology, Hyderabad took advantage (Tetrahedron Lett. 2011, 52, 5926) of the directing ability of the amide to effect selective ortho acetoxylation of 17. Similarly, Frederic Fabis of the Université de Caen Basse-Normandie used (J. Org. Chem. 2011, 76, 6414) the methoxime of 19 to direct ortho bromination, leading to 20. Teck-Peng Loh of Nanyang Technological University showed (Chem. Commun. 2011, 47, 10458) that the carbamate of 21 directed ortho C–H functionalization to give the ester 23. Yoichiro Kuninobu and Kazuhiko Takai of Okayama University rearranged (Chem. Commun. 2011, 47, 10791) the allyl ester 24 directly to the ortho-allylated acid 25. Youhong Hu of the Shanghai Institute of Materia Medica (J. Org. Chem. 2011, 76, 8495) and Graham J. Bodwell of Memorial University (J. Org. Chem. 2011, 76, 9015) condensed a chromene 26 with a nucleophile 27 to give the arene 28. C.V. Ramana of the National Chemical Laboratory prepared (Tetrahedron Lett. 2011, 52, 4627) the arene 31 by condensing 29 with 30 with high regioselectivity.
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Conference papers on the topic "Chroman derivatives synthesis"

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Stankovicová, Henrieta, Radoslav Flašík, Jana Donovalová, and Anton Gáplovský. "New 2H-chromen-2-one Derivatives Potentially Utilizable as Memory Media." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01210.

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Ghafuri, Hossein, mahsan zargari, Parya Lotfi, and Atefeh Emami. "Graphene-based polymer nanocomposite catalyzed one pot multi-component synthesis of chromene derivatives." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a004.

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Nikalje, Anna Pratima, Shailee Tiwari, Julio Seijas Vázquez, and M. Pilar Vazquez-Tato. "Ionic Liquid Mediated Synthesis Of Novel Chromone-Pyrimidine Coupled Derivatives." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04826.

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Maleki, Ali, and Vahid Eskandarpour. "Cellulose@Fe2O3-SO3H: A Novel Magnetic Composite Nanomaterial for the Synthesis of Chromene Derivatives." In 1st International Electronic Conference on Materials. MDPI, 2014. http://dx.doi.org/10.3390/ecm-1-b004.

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Javanshir, Shahrzad, and Mohammad Farhadnia. "Cellulose-Supported Metal Nanocomposite as a Green and Reusable Catalyst for One-Pot Multicomponent Synthesis of 2-Amino-4H-Chromene Derivatives." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a019.

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Maleki, Ali, and Sepide Azadegan. "Preparation and characterization of silica-supported magnetic nanocatalyst and application in the synthesis of 2-amino-4H-chromene-4-carboxylate and 2-amino-5H-pyrano[3,2-c]chromene-4-carboxylate derivatives." In The 19th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a017.

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Cortés, Iván, Andrea Bracca, and Teodoro Kaufman. "Short and efficient first total synthesis of the natural product chromanone A, a chromone derivative from the algicolous marine fungus <em>Penicillium</em> sp." In The 24th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08300.

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