2024-03-29T11:49:13Zhttp://digital.csic.es/dspace-oai/requestoai:digital.csic.es:10261/309192016-08-09T10:03:26Zcom_10261_33com_10261_5col_10261_286
2011-01-04T14:08:28Z
urn:hdl:10261/30919
Synthesis of L-chiro-inositol and (−)-conduritol F from D -sorbitol by a highly stereoselective intramolecular pinacol coupling promoted by samarium diiodide
Chiara, José Luis
Valle, Nuria
4 páginas, 1 figura.
A synthesis of L-chiro-inositol and (−)-conduritol F starting from readily available D -sorbitol is described. The route involves as a key step an efficient one-pot sequence consisting of the Swern oxidation of a 1,6-diol followed by a highly stereoselective intramolecular pinacol coupling of the resultant dialdehyde, promoted by samarium diiodide.
2011-01-04T14:08:28Z
2011-01-04T14:08:28Z
1995-08
artículo
Tetrahedron Asymmetry 6(8): 1895-1898 (1995)
0957-4166
http://hdl.handle.net/10261/30919
10.1016/0957-4166(95)00246-L
eng
http://dx.doi.org/10.1016/0957-4166(95)00246-L
closedAccess
Elsevier