Intramolecular Staudinger Ligation: A Powerful Ring‐Closure Method To Form Medium‐Sized Lactams
- 17 September 2003
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 42 (36) , 4373-4375
- https://doi.org/10.1002/anie.200351930
Abstract
No abstract availableKeywords
This publication has 33 references indexed in Scilit:
- Protein Assembly by Orthogonal Chemical Ligation MethodsJournal of the American Chemical Society, 2003
- Studies on the synthesis of cyclic pentapeptides as LHRH antagonists and the factors that influence cyclization yieldJournal of Peptide Science, 2002
- Staudinger Ligation of α-Azido Acids Retains StereochemistryThe Journal of Organic Chemistry, 2002
- Cyclic Peptides as Molecular Adapters for a Pore-Forming ProteinJournal of the American Chemical Society, 2000
- Cell Surface Engineering by a Modified Staudinger ReactionScience, 2000
- Synthesis and Application of Unprotected Cyclic Peptides as Building Blocks for Peptide DendrimersJournal of the American Chemical Society, 1997
- Chemoselective backbone cyclization of unprotected peptidesChemical Communications, 1997
- Synthesis of Proteins by Native Chemical LigationScience, 1994
- Conformation and Biological Activity of Cyclic PeptidesAngewandte Chemie International Edition in English, 1982
- Staudinger reaction between triarylphosphines and azides. MechanismJournal of the American Chemical Society, 1967