Synthesis of 3-carboxycoumarins at room temperature in water extract of banana peels

Ajani OO, Nwinyi OC (2010) Microwave-assisted synthesis and evaluation of antimicrobial activity of 3-{3-(s-aryl and s-heteroaromatic) acryloyl}-2H-chromen-2-one derivatives. J Heterocycl Chem 47:179–187. doi: 10.1002/jhet.298

Alvim J Jr, Dias RL, Castilho MS, Oliva G, Corrêa AG (2005) Preparation and evaluation of a coumarin library towards the inhibitory activity of the enzyme gGAPDH from Trypanosoma cruzi. J Braz Chem Soc 16:763–773. doi: 10.1590/S0103-50532005000500014

Andrade LH, Utsunomiya RS, Omori AT, Porto AL, Comasseto JV (2006) Edible catalysts for clean chemical reactions: bioreduction of aromatic ketones and biooxidation of secondary alcohols using plants. J Mol Catal B Enzym 38:84–90. doi: 10.1016/j.molcatb.2005.11.009

Baldassarre F, Bertoni G, Chiappe C, Marioni F (2000) Preparative synthesis of chiral alcohols by enantioselective reduction with Daucus carota root as biocatalyst. J Mol Catal B Enzym 11:55–58. doi: 10.1016/S1381-1177(00)00189-2

Bandgar BP (1999) Solvent-free one-pot rapid synthesis of 3-carboxycoumarins using focused microwaves. Green Chem 1:243–245. doi: 10.1039/A905811G

Bandgar BP, Uppalla LS, Sadavarte VS (2002) Lithium perchlorate and lithium bromide catalysed solvent free one pot rapid synthesis of 3-carboxycoumarins under microwave irradiation. J Chem Res 2002:40–41. doi: 10.3184/030823402103170402

Bennamane M, Zeror S, Aribi-Zouioueche L (2015) Asymmetric reduction of ketones by biocatalysis using clementine mandarin (citrus reticulata) fruit grown in Annaba or by ruthenium catalysis for access to both enantiomers. Chirality 27:205–210. doi: 10.1002/chir.22413

Boruah PR, Ali AA, Saikia B, Sarma D (2015) A novel green protocol for ligand free Suzuki-Miyaura cross-coupling reactions in WEB at room temperature. Green Chem 17:1442–1445. doi: 10.1039/c4gc02522a

Chanda A, Fokin VV (2009) Organic synthesis “on water”. Chem Rev 109:725–748. doi: 10.1021/cr800448q

Chandraá Barua N (2015) H 2 O 2 in WEB: a highly efficient catalyst system for the Dakin reaction. Green Chem 17:4533–4536. doi: 10.1039/c5gc01404b

Chavan HV, Bandgar BP (2013) Aqueous extract of acacia concinna pods: an efficient surfactant type catalyst for synthesis of 3-carboxycoumarins and cinnamic acids via Knoevenagel condensation. ACS Sustain Chem Eng 1:929–936. doi: 10.1021/sc4000237

Chimenti F, Bizzarri B, Bolasco A, Secci D, Chimenti P, Granese A, Carradori S, Rivanera D, Zicari A, Scaltrito MM, Sisto F (2010) Synthesis, selective anti-Helicobacter pylori activity, and cytotoxicity of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides. Bioorg Med Chem Lett 20:4922–4926. doi: 10.1016/j.bmcl.2014.04.066

Deka DC, Talukdar NN (2007) Chemical and spectroscopic investigation of Kolakhar and its commercial importance. Ind J Tradit Knowl 6:72–78

Gašo-Sokač D, Bušić V, Cetina M, Jukić M (2014) An efficient synthesis of pyridoxal oxime derivatives under microwave irradiation. Molecules 19(6):7610–7620

Gupta M, Paul S, Gupta R (2010) General aspects of 12 basic principles of green chemistry with applications. Curr Sci 99:1341–1360

He X, Shang Y, Yu Z, Fang M, Zhou Y, Han G, Wu F (2014) FeCl3-Catalyzed four-component nucleophilic addition/intermolecular cyclization yielding polysubstituted pyridine derivatives. J Org Chem 79:8882–8888. doi: 10.1021/jo5014383

Hekmatshoar R, Rezaei A, Beheshtiha SS (2009) Silica sulfuric acid: a versatile and reusable catalyst for synthesis of coumarin-3-carboxylic acids in a solvent less system. Phosphorus Sulfur Silicon 184:2491–2496. doi: 10.1080/10426500802505580

Himaja M, Poppy D, Asif K (2011) Green technique-solvent free synthesis and its advantages. Int J Res Ayurveda Pharm 2:1079–1086

Hoult JRS, Paya M (1996) Pharmacological and biochemical actions of simple coumarins: natural products with therapeutic potential. Gen Pharmacol: Vasc Syst 27:713–722. doi: 10.1016/0306-3623(95)02112-4

Karami B, Farahi M, Khodabakhshi S (2012) Rapid synthesis of novel and known coumarin-3-carboxylic acids using stannous chloride dihydrate under solvent-free conditions. Helv Chim Acta 95:455–460. doi: 10.1002/hlca.201100342

Kempen I, Papapostolou D, Thierry N, Pochet L, Counerotte S, Masereel B, Foidart JM, Reboud-Ravaux M, Noël A, Pirotte B (2003) 3-Bromophenyl 6-acetoxymethyl-2-oxo-2H-1-benzopyran-3-carboxylate inhibits cancer cell invasion in vitro and tumour growth in vivo. Br J Cancer 88:1111–1118. doi: 10.1038/sj.bjc.6600856

Kempen I, Hemmer M, Counerotte S, Pochet L, De Tullio P, Foidart JM, Blacher S, Noël A, Frankenne F, Pirotte B (2008) 6-Substituted 2-oxo-2H-1-benzopyran-3-carboxylic acid derivatives in a new approach of the treatment of cancer cell invasion and metastasis. Eur J Med Chem 43:2735–2750. doi: 10.1016/j.ejmech.2008.01.024

Koeller KM, Wong CH (2001) Enzymes for chemical synthesis. Nature 409:232–240. doi: 10.1038/35051706

Mironowicz A (1998) Biotransformations of racemic acetates by potato and topinambur tubers. Phytochemistry 47:1531–1534. doi: 10.1016/S0031-9422(97)00758-9

Myung N, Connelly S, Kim B, Park SJ, Wilson IA, Kelly JW, Choi S (2013) Bifunctional coumarin derivatives that inhibit transthyretin amyloidogenesis and serve as fluorescent transthyretin folding sensors. Chem Commun 49:9188–9190. doi: 10.1039/C3CC44667K

Neog SR, Deka CD (2013) Salt substitute from banana plant (Musa Balbiciana Colla). J Chem Pharm Res 5:155–159

Pal R (2013) Fruit juice: a natural, green and biocatalyst system in organic synthesis. Open J Org Chem 1:47–56. doi: 10.12966/ojoc.10.02.2013

Rekhaá Boruah P, AzizáAli A (2015) Pd (OAc) 2 in WERSA: a novel green catalytic system for Suzuki-Miyaura cross-coupling reactions at room temperature. Chem Commun 51:11489–11492. doi: 10.1039/C5CC04561D

Seddighi M, Shirini F, Mamaghani M (2013) Sulfonated rice husk ash (RHA-SO 3 H) as a highly efficient and reusable catalyst for the synthesis of some bis-heterocyclic compounds. RSC Adv 3:24046–24053. doi: 10.1039/C3RA44053B

Shaabani A, Ghadari R, Rahmati A, Rezayan AH (2009) Coumarin synthesis via Knoevenagel condensation reaction in 1, 1, 3, 3-N, N, N′, N′-tetramethylguanidinium trifluoroacetate ionic liquid. J Iran Chem Soc 6:710–714. doi: 10.1007/BF03246160

Silver GM, Fall R (1991) Enzymatic synthesis of isoprene from dimethylallyl diphosphate in aspen leaf extracts. Plant Physiol 97:1588–1591

Undale KA, Gaikwad DS, Shaikh TS, Desai UV, Pore DM (2012) Potassium phosphate catalyzed efficient synthesis of 3-carboxycoumarins. Indian J Chem–Part B Org Incl Med 51:1039

Vekariya RH, Patel HD (2014) Recent advances in the synthesis of coumarin derivatives via knoevenagel condensation: a review. Synth Commun 44:2756–2788. doi: 10.1080/00397911.2014.926374

Wang CJ, Hsieh YJ, Chu CY, Lin YL, Tseng TH (2002) Inhibition of cell cycle progression in human leukemia HL-60 cells by esculetin. Cancer Lett 183:163–168. doi: 10.1016/S0304-3835(02)00031-9

Zhou X, Wang XB, Wang T, Kong LY (2008) Design, synthesis, and acetylcholinesterase inhibitory activity of novel coumarin analogues. Bioorg Med Chem 16:8011–8021. doi: 10.1016/j.bmc.2008.07.068