A highly efficient method for the synthesis of guanidinium derivatives
- 21 January 2002
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 43 (4), 565-567
- https://doi.org/10.1016/s0040-4039(01)02165-7
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Coupling Rational Design with Libraries Leads to the Production of an ATP Selective ChemosensorJournal of the American Chemical Society, 2000
- Solid‐Phase Organic SynthesisPublished by Wiley ,1999
- Solid phase synthesis of oligomeric guanidiniumsTetrahedron, 1998
- Design, synthesis and evaluation of synthetic receptors for the recognition of aspartate pairs in an α-helical conformationBioorganic & Medicinal Chemistry, 1997
- Facile and Efficient Guanylation of Amines Using Thioureas and Mukaiyama's ReagentThe Journal of Organic Chemistry, 1997
- Conversion of anilines to bis-Boc protected N-methylguanidinesTetrahedron Letters, 1996
- An Efficient Procedure for the Guanylation of Amines using N,N'-bis(Benzyloxycarbonyl)-S-methylisothioureaSynthetic Communications, 1996
- A Convenient Synthesis of DI-(Benzyloxycarbonyl)-Protected GuanidinesSynthetic Communications, 1996
- Conversion of Alcohols to Protected Guanidines Using the Mitsunobu ProtocolTetrahedron Letters, 1994
- A mild and efficient method for the preparation of guanidinesTetrahedron Letters, 1992