2010
DOI: 10.1134/s107042801005026x
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Catalyzed synthesis of β-amino acids esters

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Cited by 5 publications
(4 citation statements)
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“…A mixture of dimethyl maleate 2 (60.2 g, 417 mmol), montmorillonite K10 (21 g), methanol (23 cm 3 ), and diallylamine (120 g, 1.23 mol) was stirred at 40°C for 72 h [26]. The catalyst was filtered off and washed with dichloromethane (75 cm 3 ).…”
Section: Synthesis Of Monomersmentioning
confidence: 99%
“…A mixture of dimethyl maleate 2 (60.2 g, 417 mmol), montmorillonite K10 (21 g), methanol (23 cm 3 ), and diallylamine (120 g, 1.23 mol) was stirred at 40°C for 72 h [26]. The catalyst was filtered off and washed with dichloromethane (75 cm 3 ).…”
Section: Synthesis Of Monomersmentioning
confidence: 99%
“…Cephalosporins and carbapenems (Figure 1) exhibit a broad spectrum of antibacterial activity. β-Amino acid ester derivatives can be used as building blocks for the synthesis of these types of antibiotics, making them useful in drug synthesis and other fields [10,11,12,13].…”
Section: Introductionmentioning
confidence: 99%
“…β-Amino ester derivatives are key intermediate in the synthesis of β-lactam antibiotics, which are important components of many natural products and therapeutic agents [12,13,14]. Therefore, the asymmetric synthesis of β-amino ester derivatives has become a field of increasing interest in organic synthetic chemistry over the past few years [15,16,17,18,19,20].…”
Section: Introductionmentioning
confidence: 99%
“…As an extension study of our group’s research [19,21], we have now synthesized a series of novel β-amino ester derivatives containing benzofuran and benzothiazole units. The structures of these newly synthesized compounds were confirmed by 1 H-NMR, 13 C-NMR, IR spectra, and MS (HREI) analysis.…”
Section: Introductionmentioning
confidence: 99%