FN Archimer Export Format
PT J
TI New access to 1,3-diketones from aldehydes
BT 
AF FARGEAS, Valérie
   BAALOUCH, Myriam
   METAY, Estelle
   BAFFREAU, Jerôme
   MENARD, Delphine
   GOSSELIN, Pascal
   BERGE, Jean-Pascal
   BARTHOMEUF, Chantal
   LEBRETON, Jacques
AS 1:;2:;3:;4:;5:;6:;7:;8:;9:;
FF 1:;2:;3:;4:;5:;6:;7:PDG-DRV-VP-GA;8:;9:;
C1 CNRS, Fac Sci & Tech, UMR 6513, Organ Synth Lab, F-44322 Nantes 3, France.
   Univ Maine, Fac Sci, CNRS, UMR 6511,Lab Synth Organ, F-72085 Le Mans, France.
   IFREMER, Dept Valorisat Prod Mer, F-44311 Nantes 3, France.
   Univ Auvergne, Fac Pharm, Lab Pharmacognosie & Biotechnol, UMR,U 484,INSERM, F-63001 Clermont Ferrand, France.
C2 CNRS, FRANCE
   UNIV MAINE, FRANCE
   IFREMER, FRANCE
   UNIV AUVERGNE, FRANCE
SI NANTES
SE PDG-DRV-VP-GA
IN WOS Ifremer jusqu'en 2018
   copubli-univ-france
IF 2.643
TC 23
UR https://archimer.ifremer.fr/doc/2004/publication-829.pdf
LA English
DT Article
DE ;1,3 diketones;Alkylation;Sulfones;Aldehydes
AB A simple and efficient methodology to introduce an 1,3-diketone motif from various aldehyde precursors in three steps with good overall yields is described using beta-ketosulphone 7 as masked equivalent of acetone. 
PY 2004
PD NOV
SO Tetrahedron
SN 0040-4020
PU Elsevier
VL 60
IS 45
UT 000224448500027
BP 10359
EP 10364
DI 10.1016/j.tet.2004.07.087
ID 829
ER

EF