Halogen-Bonding-Induced Hydrogen Transfer to CN Bond with Hantzsch Ester
Several bidentate dihydroimidazolines were prepared and investigated as catalysts for hydrogen transfer reduction of CN bond with Hantzsch ester. Highly efficient reactions were observed for quinolines and imines with low catalyst loading of 2 mol %. The presence of halogen bonding was elucidated u...
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Published in: | Organic letters Vol. 16; no. 12; pp. 3244 - 3247 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
American Chemical Society
20-06-2014
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Online Access: | Get full text |
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Summary: | Several bidentate dihydroimidazolines were prepared and investigated as catalysts for hydrogen transfer reduction of CN bond with Hantzsch ester. Highly efficient reactions were observed for quinolines and imines with low catalyst loading of 2 mol %. The presence of halogen bonding was elucidated using NMR studies and isothermal calorimeric titrations. Binding constants of the XB donors were also measured using isothermal calorimeric titrations (ITC). |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/ol501259q |