TY - JOUR
T1 - Stereocontrolled synthetic entries to homochiral hydroxylated norbornene derivatives. Formal synthesis of some carbocyclic nucleosides.
AU - Díaz, Miguel
AU - Ibarzo, Javier
AU - Jiménez, José M.
AU - Ortuño, Rosa M.
PY - 1994/1/1
Y1 - 1994/1/1
N2 - Several homochiral hydroxylated norbornene derivatives have been synthesized from D-mannitol. Stereocontrolled Diels-Alder cycloadditions and stereospecific hydroxylations are key processes for the creation of the stereogenic centers in the target molecules. These compounds are real or potential precursors in the synthesis of carbocyclic nucleosides and related products. © 1994.
AB - Several homochiral hydroxylated norbornene derivatives have been synthesized from D-mannitol. Stereocontrolled Diels-Alder cycloadditions and stereospecific hydroxylations are key processes for the creation of the stereogenic centers in the target molecules. These compounds are real or potential precursors in the synthesis of carbocyclic nucleosides and related products. © 1994.
UR - https://www.scopus.com/pages/publications/0028144276
U2 - 10.1016/S0957-4166(00)80493-0
DO - 10.1016/S0957-4166(00)80493-0
M3 - Article
SN - 0957-4166
VL - 5
SP - 129
EP - 140
JO - Tetrahedron: asymmetry
JF - Tetrahedron: asymmetry
IS - 1
ER -