Catalytic Asymmetric Dihydroxylation of Enamides and Application to the Total Synthesis of (+)??Tanikolide

B Gourdet, HW Lam

Index: Gourdet, Benoit; Lam, Hon Wai Angewandte Chemie - International Edition, 2010 , vol. 49, # 46 p. 8733 - 8737

Full Text: HTML

Citation Number: 29

Abstract

Asymmetric transformations of 1, 1-disubstituted alkenes provide important building blocks for chemical synthesis, but are often plagued with low stereoselectivities because it can be difficult for a chiral reagent or catalyst to discriminate between the enantiotopic faces of these substrates.[1] Among the available methods, asymmetric dihydroxylation (AD) stands out as one of the more successful, and can provide high enantioselectivities in certain ...

Related Articles:

Radical additions to allyl bromides. A synthetically useful,'Tin-Free'method for carbon–carbon bond formation

[Struss, John A.; Sadeghipour, Mitra; Tanko, James M. Tetrahedron Letters, 2009 , vol. 50, # 18 p. 2119 - 2120]

Remarkable Behavior of a Bifunctional Alkynylborane Zirconocene Complex toward Donor Ligands and Acetylenes

[Xu, Xin; Kehr, Gerald; Daniliuc, Constantin G.; Erker, Gerhard Journal of the American Chemical Society, 2013 , vol. 135, # 17 p. 6465 - 6476]

More Articles...