cheminform abstract: synthesis of trifluoromethanesulfinamidines and -sulfanylamides

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ChemInform 2009, 40, issue 17 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim www.cheminform.wiley-vch.de Thio compounds P 0440 Synthesis of Trifluoromethanesulfinamidines and -sulfanylamides. — Base-medi- ated treatment of the silanes (I) and (XII) with aminosulfur trifluorides and subsequent reaction with amines allows simple access to fluorinated sulfinamidines and sulfanyl- amides. Depending on the electronic nature of amine and conditions used, amidines or amides are formed. — (FERRY, A.; BILLARD*, T.; LANGLOIS, B. R.; BACQUE, E.; J. Org. Chem. 73 (2008) 23, 9362-9365; Inst. Chim. Biochim. Mol. Supramol., CNRS, Univ. Lyon 1, F-69622 Lyon, Fr.; Eng.) — Jannicke 17- 062

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www.cheminform.wiley-vch.de

Thio compoundsP 0440 Synthesis of Trifluoromethanesulfinamidines and -sulfanylamides. — Base-medi-

ated treatment of the silanes (I) and (XII) with aminosulfur trifluorides and subsequent reaction with amines allows simple access to fluorinated sulfinamidines and sulfanyl-amides. Depending on the electronic nature of amine and conditions used, amidines or amides are formed. — (FERRY, A.; BILLARD*, T.; LANGLOIS, B. R.; BACQUE, E.; J. Org. Chem. 73 (2008) 23, 9362-9365; Inst. Chim. Biochim. Mol. Supramol., CNRS, Univ. Lyon 1, F-69622 Lyon, Fr.; Eng.) — Jannicke

17- 062

ChemInform 2009, 40, issue 17 © 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim