IRIS publication 726126
Enantioselective Intramolecular Buchner Reaction of alpha-Diazoketones
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TY - JOUR - O'Keeffe, S, Harrington, F, Maguire, AR - 2007 - July - Synlett - Enantioselective Intramolecular Buchner Reaction of alpha-Diazoketones - Validated - () - -1 - 15 - 2367 - 2370 - Enantioselectivities of up to 95% ee have been achieved in the intrarnolecular Buchner reaction catalysed by copper is oxazoline) complexes, the highest asymmetric inductions reported to date for this transformation. Significantly, use of a catalyst derived from a bis(oxazoline) ligand resulted in high enantioselectivities across several Substrates, indicating the possibility of developing a catalyst with general applicability.. - DOI 10.1055/s-2007-986626 DA - 2007/07 ER -
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@article{V726126, = {O'Keeffe, S and Harrington, F and Maguire, AR }, = {2007}, = {July}, = {Synlett}, = {Enantioselective Intramolecular Buchner Reaction of alpha-Diazoketones}, = {Validated}, = {()}, = {-1}, = {15}, pages = {2367--2370}, = {{Enantioselectivities of up to 95% ee have been achieved in the intrarnolecular Buchner reaction catalysed by copper is oxazoline) complexes, the highest asymmetric inductions reported to date for this transformation. Significantly, use of a catalyst derived from a bis(oxazoline) ligand resulted in high enantioselectivities across several Substrates, indicating the possibility of developing a catalyst with general applicability..}}, = {DOI 10.1055/s-2007-986626}, source = {IRIS} }
Data as stored in IRIS
AUTHORS | O'Keeffe, S, Harrington, F, Maguire, AR | ||
YEAR | 2007 | ||
MONTH | July | ||
JOURNAL_CODE | Synlett | ||
TITLE | Enantioselective Intramolecular Buchner Reaction of alpha-Diazoketones | ||
STATUS | Validated | ||
TIMES_CITED | () | ||
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VOLUME | -1 | ||
ISSUE | 15 | ||
START_PAGE | 2367 | ||
END_PAGE | 2370 | ||
ABSTRACT | Enantioselectivities of up to 95% ee have been achieved in the intrarnolecular Buchner reaction catalysed by copper is oxazoline) complexes, the highest asymmetric inductions reported to date for this transformation. Significantly, use of a catalyst derived from a bis(oxazoline) ligand resulted in high enantioselectivities across several Substrates, indicating the possibility of developing a catalyst with general applicability.. | ||
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DOI_LINK | DOI 10.1055/s-2007-986626 | ||
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