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ChemInform Abstract: [2, 3]‐Sigmatropic Rearrangement of Allylic Selenimides: Strategy for the Synthesis of Peptides, Peptidomimetics, and N‐Aryl Vinyl Glycines. Issue 39 (23rd September 2014)
Record Type:
Journal Article
Title:
ChemInform Abstract: [2, 3]‐Sigmatropic Rearrangement of Allylic Selenimides: Strategy for the Synthesis of Peptides, Peptidomimetics, and N‐Aryl Vinyl Glycines. Issue 39 (23rd September 2014)
Main Title:
ChemInform Abstract: [2, 3]‐Sigmatropic Rearrangement of Allylic Selenimides: Strategy for the Synthesis of Peptides, Peptidomimetics, and N‐Aryl Vinyl Glycines.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The scope of the NCS‐mediated amination/[2, 3]‐sigmatropic rearrangement of enantioenriched allylic selenides is expanded to provide access to the product classes listed in title.</p> </abstract>