Enantioselective formation of quaternary stereocenters using the catalytic intramolecular Stetter reaction
JL Moore, MS Kerr, T Rovis
Index: Moore, Jennifer L.; Kerr, Mark S.; Rovis, Tomislav Tetrahedron, 2006 , vol. 62, # 49 p. 11477 - 11482
Full Text: HTML
Citation Number: 58
Abstract
Catalytic carbon–carbon bond formation resulting in the creation of a quaternary stereocenter is a useful but challenging tool in organic chemistry. 1, 1a, 1b and 1c In addition to established approaches using chiral auxiliaries, 2, 2a and 2b significant progress has been made in recent years aimed at catalytic methods for the formation of quaternary stereocenters. These include the intramolecular Heck reaction, 3 rearrangement of enol carbonates, 4, 4a and 4b ...
Related Articles:
Thiazol-2-ylidene catalysis in intramolecular crossed aldehyde-ketone benzoin reactions
[Enders, Dieter; Niemeier, Oliver Synlett, 2004 , # 12 p. 2111 - 2114]
[Richard, John P.; Nagorski Journal of the American Chemical Society, 1999 , vol. 121, # 20 p. 4763 - 4770]
[Schiess, Peter; Huys-Francotte, Martine; Vogel, Caspar Tetrahedron Letters, 1985 , vol. 26, # 33 p. 3959 - 3962]