Erratum: Synthesis of chiral vicinal C2 symmetric and unsymmetric bis(sulfonamide) ligands based on trans-1,2-cyclohexanediamine by aminolysis of N-tosylaziridines (Tetrahedron Letters (2005) 46 (7935) DOI: 10.1016/j.tetlet.2005.09.089);Synthesis of chiral vicinal C2 symmetric and unsymmetric bis(sulfonamide) ligands based on trans-1,2-cyclohexanediamine by aminolysis of N-tosylaziridines

Tetrahedron Letters

Volumn 46, Issue 46, 2005, Pages 7935-7939

  Bisai, Alakesh ^a   Prasad, B A Bhanu ^a   Singh, Vinod K ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY KANPUR   (India)

Author keywords

Aminolysis; Aziridines; Chiral C2 symmetric and unsymmetric ligands; Sulfonamide ligands

Indexed keywords

1,2 DIAMINOCYCLOHEXANE; ALIPHATIC AMINE; AMINE; AZIRIDINE DERIVATIVE; DIAMINE; LIGAND; LITHIUM; SULFONAMIDE; TOLUENESULFONIC ACID DERIVATIVE;

AMINOLYSIS; ARTICLE; ASYMMETRIC SYNTHESIS; CATALYSIS; CHIRALITY; METHODOLOGY; RING OPENING;

EID: 26844479520     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.12.052     Document Type: Erratum

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48. 4 (0.1 mmol) in anhydrous acetonitrile (6 mL) under an argon atmosphere at rt. The reaction mixture was refluxed until completion of the reaction (usually 4-8 h, monitoring by TLC). Most of the acetonitrile was removed in vacuo and the crude reaction mixture was partitioned between EtOAc and water. The organic layer was washed with water, brine and dried over anhydrous sodium sulfate. It was concentrated in vacuo to give a crude product, which was purified by silica gel column chromatography using EtOAc and hexane to give the pure vicinal aminosulfonamide.
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