Enantioselective annulation reactions of bisenolates prepared through dearomatization reactions of aromatic and heteroaromatic diesters
J Pérez??Vázquez, AX Veiga, G Prado…
Index: Perez-Vazquez, Jaime; Veiga, Alberte X.; Prado, Gustavo; Sardina, F. Javier; Paleo, M. Rita European Journal of Organic Chemistry, 2012 , # 5 p. 975 - 987
Full Text: HTML
Citation Number: 2
Abstract
Abstract A one-pot, enantioselective strategy for the dearomatization–annulation of aromatic diesters to give a range of highly functionalized polycyclic molecules with excellent enantioselectivity is presented. This methodology is based on the reaction of bisenolates, prepared by treating aromatic diesters with trialkyltin lithium reagents, which involves a stanna-Brook rearrangement, with 1, ω-dihaloalkanes and other biselectrophiles. We ...
Related Articles:
High-yield syntheses of 2, 3-disubstituted furans and thiophenes
[Carpenter, Andrew J.; Chadwick, Derek J Tetrahedron Letters, 1985 , vol. 26, # 14 p. 1777 - 1780]
2, 3-Furan, pyrrole and thiophenedicarboxylic acids
[Jones Journal of the American Chemical Society, 1955 , vol. 77, p. 4069,4072]
2, 3-Furan, pyrrole and thiophenedicarboxylic acids
[Jones Journal of the American Chemical Society, 1955 , vol. 77, p. 4069,4072]
One-step synthesis of furan-2, 5-dicarboxylic acid from furan-2-carboxylic acid using carbon dioxide
[Fischer, Robert; Fiserova, Maria Arkivoc, 2013 , vol. 2013, # 4 p. 405 - 412]
High-yield syntheses of 2, 3-disubstituted furans and thiophenes
[Carpenter, Andrew J.; Chadwick, Derek J Tetrahedron Letters, 1985 , vol. 26, # 14 p. 1777 - 1780]