10080-41-8Relevant articles and documents
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Doering,DePuy
, p. 5955 (1953)
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Amino- and azidocarbonylation of iodoalkenes
Mikle, Gábor,Skoda-F?ldes, Rita,Kollár, László
, (2021/10/14)
Iodoalkenes, available from ketones via their hydrazones, underwent palladium-catalysed azidocarbonylation. Depending on the structure of the acyl azides, consecutive hydrolysis toward corresponding primary amides was observed. ‘Direct’ aminocarbonylation
ALKENE MIMICS
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Page/Page column 19-20, (2010/10/20)
Ac-Phe-Tyr-phosphoSer-Ψ[CH=C]-Pro-Arg-NH2AND Fmoc-bis(pivaloylmethoxy)phosphoSer-Ψ[CH=C]-Pro-2-aminoethyl-(3-indole); and their Phospho-(D)-serine stereoisomers are novel compounds. Ψ refers to a pseudo amide. Such novel compounds advantageousl
Serine-cis-proline and serine-trans-proline isosteres: Stereoselective synthesis of (Z)- and (E)-alkene mimics by Still-Wittig and Ireland-Claisen rearrangements
Wang, Xiaodong J.,Hart, Scott A.,Xu, Bailing,Mason, Matthew D.,Goodell, John R.,Etzkorn, Felicia A.
, p. 2343 - 2349 (2007/10/03)
Two new amide isosteres of Ser-cis-Pro and Ser-trans-Pro dipeptides were designed and stereo-selectively synthesized to be incorporated into potential inhibitors of the phosphorylation-dependent peptidylprolyl isomerase Pin1, an essential regulator of the