2018
DOI: 10.2174/1386207321666180315095422
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DABCO Catalyzed Green and Efficient Synthesis of 2-Amino-4H-Pyrans and Their Biological Evaluation as Antimicrobial and Anticancer Agents

Abstract: The present method is simple, rapid, and most efficient green protocol for the synthesis of 2-amino-4H-pyran derivatives using highly inexpensive and easily available DABCO as an efficient catalyst under grinding and solvent free condition at room temperature.

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Cited by 8 publications
(1 citation statement)
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“…Given the importance of these compounds, many catalyst have been developed for the synthesis of 2-amino-3-cyano-4 H -pyran such as Fe 3 O 4 @SiO 2 @GPTMS@guanidine, 31 Fe 3 O 4 @GA@IG, 32 Fe 3 O 4 @SiO 2 –NH 2 @TCT–guanidine, 33 boron nitride@Fe 3 O 4 , 34 montmorillonite, 35 GO-Fc@Fe 3 O 4 , 36 [EMIM][OH], 37 nano-SnO 2 , 38 sodium alginate, 39 [PEG(mim) 2 ][OH] 2 , 40 iodine, 41 cesium fluoride, 42 MNPs@Cu, 43 DABCO, 44 CeCl 3 ·7H 2 O, 45 Fe 3 O 4 @GA@IG, 46 EDA/(CH 2 ) 3 @SiO 2 @Fe 3 O 4 , 47 NH 4 H 2 PO 4 /Al 2 O 3 , 48 NiFe 2 O 4 @SiO 2 @H 14 [NaP 5 W 30 O 110 ], 49 Ag/Fe 3 O 4 @starch, 50 per-6-NH 2 –β-CD, 51 Fe 3 O 4 @NH 2 @TCT@HOProCu, 52 and molecular iodine. 53 Despite some advantages of the reported methods, some of them suffer from various limitations such as high temperatures, reflux conditions, expensive reagents, harsh reaction conditions, extended reaction times, generation of waste materials, tedious work-up procedures, and low yields.…”
Section: Introductionmentioning
confidence: 99%
“…Given the importance of these compounds, many catalyst have been developed for the synthesis of 2-amino-3-cyano-4 H -pyran such as Fe 3 O 4 @SiO 2 @GPTMS@guanidine, 31 Fe 3 O 4 @GA@IG, 32 Fe 3 O 4 @SiO 2 –NH 2 @TCT–guanidine, 33 boron nitride@Fe 3 O 4 , 34 montmorillonite, 35 GO-Fc@Fe 3 O 4 , 36 [EMIM][OH], 37 nano-SnO 2 , 38 sodium alginate, 39 [PEG(mim) 2 ][OH] 2 , 40 iodine, 41 cesium fluoride, 42 MNPs@Cu, 43 DABCO, 44 CeCl 3 ·7H 2 O, 45 Fe 3 O 4 @GA@IG, 46 EDA/(CH 2 ) 3 @SiO 2 @Fe 3 O 4 , 47 NH 4 H 2 PO 4 /Al 2 O 3 , 48 NiFe 2 O 4 @SiO 2 @H 14 [NaP 5 W 30 O 110 ], 49 Ag/Fe 3 O 4 @starch, 50 per-6-NH 2 –β-CD, 51 Fe 3 O 4 @NH 2 @TCT@HOProCu, 52 and molecular iodine. 53 Despite some advantages of the reported methods, some of them suffer from various limitations such as high temperatures, reflux conditions, expensive reagents, harsh reaction conditions, extended reaction times, generation of waste materials, tedious work-up procedures, and low yields.…”
Section: Introductionmentioning
confidence: 99%