2008
DOI: 10.1016/j.bmcl.2007.11.035
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An efficient, simple and expedition synthesis of 1-amidoalkyl-2-naphthols as ‘drug like’ molecules for biological screening

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Cited by 154 publications
(50 citation statements)
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“…It was shown that the aromatic aldehydes with electron withdrawing groups reacted faster than their analogues with electron releasing groups. In contrast to the previously reported methods [10,11] , in which aliphatic aldehydes were not transformed into the corresponding 1-amidoalkyl-2-naphtols, they were converted into the desired product in good yields in the current methodology. Findings revealed that this protocol is effective for a wide range of aldehydes.…”
Section: Synthesis Of Different α-Amidoakyl-β-naphtols In the Presencmentioning
confidence: 58%
“…It was shown that the aromatic aldehydes with electron withdrawing groups reacted faster than their analogues with electron releasing groups. In contrast to the previously reported methods [10,11] , in which aliphatic aldehydes were not transformed into the corresponding 1-amidoalkyl-2-naphtols, they were converted into the desired product in good yields in the current methodology. Findings revealed that this protocol is effective for a wide range of aldehydes.…”
Section: Synthesis Of Different α-Amidoakyl-β-naphtols In the Presencmentioning
confidence: 58%
“…These 1-amidoalkyl-2-naphthol and tetrahydrobenzo [b]pyran derivatives are of particular value because of their promising biological and pharmacological activities [7][8][9]. The preparation of amidoalkyl naphthols has been carried out by a three-component condensation of aldehydes, 2-naphthols and amides using different catalysts such as Ba 3 (PO 4 ) 2 [10], Nano Al 2 O 3 [11], supported heteropolyacid [12,13], magnetic sulfonic or phosphoric acid [14][15][16], β-CD-BSA [17], [C 6 [18], MWCNT@Co-complex [19], sulfonated polynapthalene [20] and grapheme oxide [21] in the last five years.Despite undeniable advantages of these methods, a great part of themsuffer from one or more shortcomings such as high reaction temperature, prolonged reaction time, low yield and difficult catalyst separation and recovery.…”
Section: Introductionmentioning
confidence: 99%
“…Although numerous methods for the synthesis of 1-amidoalkyl-2-naphthols have been reported, [3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22] there is still demand for simpler, less toxic, more effective, and milder catalysts. Our interest in developing a mild and efficient synthetic method that provides a variety of 1-amidoalkyl-2-naphthols has led us to looking into more convenient and safely usable catalysts.…”
mentioning
confidence: 99%