Tetrahedron letters

Palladium-catalyzed synthesis of amides and peptides

EC Roos, P Bernabé, H Hiemstra, WN Speckamp…

Index: Roos, Eric C.; Bernabe, Pablo; Hiemstra, Henk; Speckamp, W. Nico Tetrahedron Letters, 1991 , vol. 32, # 45 p. 6633 - 6636

Full Text: HTML

Citation Number: 15

Abstract

Abstract When the Pd (0)-catalyzed hydrostannolysis of the N-allyloxycarbonyl group is carried out in the presence of an activated carbonyl compound, a coupling product is formed. This new method appears to be applicable to the synthesis of a wide range of amides and peptides.

Related Articles:

Synthesis of dipeptides from N-hydroxy-3-azaspiro [5, 5] undecane-2, 4-dione activated α-amino acids

[Nowshuddin, Shaik; Ram Reddy Tetrahedron Asymmetry, 2011 , vol. 22, # 1 p. 22 - 25]

Palladium-catalyzed transprotection of allyloxycarbonyl-protected amines: efficient one-pot formation of amides and dipeptides

[Roos; Bernabe; Hiemstra; Speckamp; Kaptein; Boesten Journal of Organic Chemistry, 1995 , vol. 60, # 6 p. 1733 - 1740]

Palladium-catalyzed transprotection of allyloxycarbonyl-protected amines: efficient one-pot formation of amides and dipeptides

[Roos; Bernabe; Hiemstra; Speckamp; Kaptein; Boesten Journal of Organic Chemistry, 1995 , vol. 60, # 6 p. 1733 - 1740]

Oxidation of peptides by methyl (trifluoromethyl) dioxirane: the protecting group matters

[Rella, Maria Rosaria; Williard, Paul G. Journal of Organic Chemistry, 2007 , vol. 72, # 2 p. 525 - 531]

Oxidation of peptides by methyl (trifluoromethyl) dioxirane: the protecting group matters

[Rella, Maria Rosaria; Williard, Paul G. Journal of Organic Chemistry, 2007 , vol. 72, # 2 p. 525 - 531]

More Articles...