Related Articles:

Asymmetric hydrogenation of olefins with aprotic oxygen functionalities catalyzed by BINAP-Ru (II) complexes

[Journal of Organic Chemistry, , vol. 60, # 2 p. 357 - 363]

Studies on structurally simple α, β-butenolides—II:(−)-(S)-γ-hydroxymethyl-α, β-butenolide and derivatives from d-ribonolactone efficient synthesis of (−)-ranunculin

[Camps, P.; Cardellach, J.; Font, J.; Ortuno, R. M.; Ponsati, O Tetrahedron, 1982 , vol. 38, # 15 p. 2395 - 2402]

Enantioselective hydrogenation of levulinic acid esters in the presence of the RuII-BINAP-HCl catalytic system

[Russian Chemical Bulletin, , vol. 54, # 10 p. 2374 - 2378]

Kinetic study of asymmetric hydrogenation of methyl levulinate using the (COD) Ru (2-methylallyl) 2–BINAP–HCl catalytic system

[Juszkiewicz; Asztemborska; Jurczak Polish Journal of Chemistry, 2002 , vol. 76, # 12 p. 1707 - 1711]

Enantiospecific preparation of the lactone fragment of murisolin

[Harmange, Jean-Christophe; Figadere, Bruno; Hocquemiller, Reynald Tetrahedron: Asymmetry, 1991 , vol. 2, # 5 p. 347 - 350]