Enantioselective straightforward access to benzo [b] thiophene analogs of Azatoxin
…, J Rey, F Popowycz, S Pellet-Rostaing, M Lemaire
Index: Gracia, Stephanie; Marion, Cedric; Rey, Jullien; Popowycz, Florence; Pellet-Rostaing, Stephane; Lemaire, Marc Tetrahedron Letters, 2012 , vol. 53, # 25 p. 3165 - 3168
Full Text: HTML
Citation Number: 3
Abstract
Horner-Wadsworth Emmons olefination followed by asymmetric hydrogenation allowed the first synthetic access to the chiral thiotryptophan with good enantiomeric excess. Oxazolidinone formation followed by a Pictet–Spengler condensation provided the benzothiophenic analog of Azatoxin.
Related Articles:
Palladium??Catalyzed Reductive Carbonylation of Aryl Bromides with Phosphinite Ligands
[Neumann, Helfried; Kadyrov, Renat; Wu, Xiao-Feng; Beller, Matthias Chemistry - An Asian Journal, 2012 , vol. 7, # 10 p. 2213 - 2216]
Synthesis of aromatic aldehydes by oxidative hydroxymethylation
[Synlett, , # 9 p. 1575 - 1576]
The Interaction of Heteroaryl??Acrylates and Alanines with Phenylalanine Ammonia??Lyase from Parsley
[Paizs, Csaba; Katona, Adrian; Retey, Janos Chemistry - A European Journal, 2006 , vol. 12, # 10 p. 2739 - 2744]
The Interaction of Heteroaryl??Acrylates and Alanines with Phenylalanine Ammonia??Lyase from Parsley
[Chemistry - A European Journal, , vol. 12, # 10 p. 2739 - 2744]