Enantioselective Intramolecular Buchner Reaction of alpha-Diazoketones

Typeset version

 

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  - 
@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}
}
AUTHORSO'Keeffe, S, Harrington, F, Maguire, AR
YEAR2007
MONTHJuly
JOURNAL_CODESynlett
TITLEEnantioselective Intramolecular Buchner Reaction of alpha-Diazoketones
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORD
VOLUME-1
ISSUE15
START_PAGE2367
END_PAGE2370
ABSTRACTEnantioselectivities 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..
PUBLISHER_LOCATION
ISBN_ISSN
EDITION
URL
DOI_LINKDOI 10.1055/s-2007-986626
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