1995
DOI: 10.1016/0957-4166(94)00385-o
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A convenient preparation of 2-substituted (S)-aziridines

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Cited by 22 publications
(11 citation statements)
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“…1 Their analytic data are identical to the reported ones. [1][2][3][4][5][6][7][8] Other reactants are commercial available and were used without further purification. All solvents were used without purification.…”
Section: Methodsmentioning
confidence: 99%
“…1 Their analytic data are identical to the reported ones. [1][2][3][4][5][6][7][8] Other reactants are commercial available and were used without further purification. All solvents were used without purification.…”
Section: Methodsmentioning
confidence: 99%
“…Cyanohydrin esters (1)(2)(3)(4)(5)(6)(7)(8) were synthesized in two consecutive reactions. Firstly, cyanohydrins were prepared from the corresponding aldehydes.…”
Section: Chemical Synthesismentioning
confidence: 99%
“…Cyanohydrins are versatile compounds with several applications as chiral building blocks. [1] In this context, they can be used as precursors of -amino alcohols, [2] α-hydroxy acids, [3] α-hydroxy ketones, [4] and other compounds with high added value in the pharmaceutical industry. [5] Cyanohydrins have already been used as precursors of different drugs, such as fluoxetine, duloxetine and its derivatives, [6] capuramycin, [7] bufuralol, [8] denopamine, and salbutamol.…”
Section: Introductionmentioning
confidence: 99%
“…Nitrilase-catalyzed hydrolysis of nitriles offers a "greener" alternative, [1] because this eco-friendly biotransformation allows the clean and mild synthesis of carboxylic acids with high yield and selectivity. [2][3][4][5][6][7][8][9][10][11][12][13][14][15] Cyanocarboxylic acids are important intermediates for a variety of applications. For example, 1-cyanocyclohexaneacetic acid is a useful precursor for the synthesis of gabapentin.…”
Section: Abstract: Cyanocarboxylic Acids; Dinitriles; Enzyme Catalysimentioning
confidence: 99%
“…The general procedure was followed: 1-Cyanocyclopentaneacetonitiles (200 mg, 1.31 mmol) was treated with the nitrilase (10 mg, 13.5 U) in potassium phosphate buffer (50 mL, 100 mM, pH 7.2). The reaction mixture was incubated at 30 8C and the reaction was monitored by 13…”
Section: Preparation Of 1-cyanocycloalkaneacetic Acidsmentioning
confidence: 99%