TY  - JOUR
  - Collins SG, O'Sullivan OC, Kelleher PG, Maguire AR
  - 2013
  - February
  - Organic ; Biomolecular Chemistry
  - Design and synthesis of stable α-diazo-β-oxo sulfoxides.
  - Validated
  - Altmetric: 1 ()
  - 11
  - 10
  - 1706
  - 1725
  - Diazo transfer adjacent to a sulfoxide moiety to provide stable, isolable a-diazo-ß-oxo sulfoxides has been achieved. Use of monocyclic and bicyclic sulfoxide precursors is critical in enabling isolation of stable derivatives, through introduction of conformational constraint, while acyclic a-diazo-ß-oxo sulfoxides are too labile to isolate and characterize.
  - 10.1039/c3ob27061k
DA  - 2013/02
ER  - 

@article{V202485800,
   = {Collins SG,  O'Sullivan OC and  Kelleher PG,  Maguire AR },
   = {2013},
   = {February},
   = {Organic ; Biomolecular Chemistry},
   = {Design and synthesis of stable α-diazo-β-oxo sulfoxides.},
   = {Validated},
   = {Altmetric: 1 ()},
   = {11},
   = {10},
  pages = {1706--1725},
   = {{Diazo transfer adjacent to a sulfoxide moiety to provide stable, isolable a-diazo-ß-oxo sulfoxides has been achieved. Use of monocyclic and bicyclic sulfoxide precursors is critical in enabling isolation of stable derivatives, through introduction of conformational constraint, while acyclic a-diazo-ß-oxo sulfoxides are too labile to isolate and characterize.}},
   = {10.1039/c3ob27061k},
  source = {IRIS}
}