2015
DOI: 10.3998/ark.5550190.p008.894
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Alumina sulfuric acid (ASA), tungstate sulfuric acid (TSA), molybdate sulfuric acid (MSA) and xanthan sulfuric acid (XSA) as solid and heterogeneous catalysts in green organic synthesis: a review

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Cited by 17 publications
(3 citation statements)
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“…However, pure SiO 2 is not active in the S-3-CR, as indicated by Iwanami et al, 32 while silica sulfuric acid (SSA, SiO 2 -SO 3 H) is very effective, as demonstrated by Chen and Lu. 46 This reusable green and inexpensive heterogeneous acid catalyst has been widely investigated [47][48][49][50][51] since 2001, when Zol-gol described its preparation by using a simple reaction of neat chlorosulfonic acid and silica gel (Fig. 2A).…”
Section: Mcm-41 and Its Derivativesmentioning
confidence: 99%
“…However, pure SiO 2 is not active in the S-3-CR, as indicated by Iwanami et al, 32 while silica sulfuric acid (SSA, SiO 2 -SO 3 H) is very effective, as demonstrated by Chen and Lu. 46 This reusable green and inexpensive heterogeneous acid catalyst has been widely investigated [47][48][49][50][51] since 2001, when Zol-gol described its preparation by using a simple reaction of neat chlorosulfonic acid and silica gel (Fig. 2A).…”
Section: Mcm-41 and Its Derivativesmentioning
confidence: 99%
“…H. Patel and col./et al reviewed the utilization of several novel heterogeneous catalysts and their use in organic synthesis, for example, alumina sulfuric acid (ASA), tungstate sulfuric acid (TSA), molybdate sulfuric acid (MSA), and xanthan sulfuric acid (XSA) [2]. These materials are economical, efficient, and compatible with the environment.…”
Section: Introductionmentioning
confidence: 99%
“…These materials are economical, efficient, and compatible with the environment. Particularly, they described the use of alumina sulfuric acid, obtained by the reaction between chlorosulfonic acid and activated neutral alumina in the synthesis of several organic compounds such as benzimidazoles, quinoxalines, nitration of aromatic compounds, synthesis of 2,5-disubstituted 1,3,4oxadiazoles, dithioacetalization, ortho-silylation of alcohols, oximes and phenols, Biginelli-type condensation reaction, and Pechmann condensation [2].…”
Section: Introductionmentioning
confidence: 99%