Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103050
Title: Halogen-bonding-induced hydrogen transfer to C═N bond with hantzsch ester
Authors: He, Wei
Ge, Yi-Cen
Tan, Choon-Hong
Keywords: DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2014
Source: He, W., Ge, Y.-C., & Tan, C.-H. (2014). Halogen-bonding-induced hydrogen transfer to C═N bond with hantzsch ester. Organic letters, 16(12), 3244-3247.
Series/Report no.: Organic letters
Abstract: Several bidentate dihydroimidazolines were prepared and investigated as catalysts for hydrogen transfer reduction of C═N 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).
URI: https://hdl.handle.net/10356/103050
http://hdl.handle.net/10220/24358
DOI: 10.1021/ol501259q
Schools: School of Physical and Mathematical Sciences 
Rights: © 2014 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Organic Letters, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [Article DOI: http://dx.doi.org/10.1021/ol501259q].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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