One step synthesis of orthogonally protected diaminodicarboxylic acids by mixed kolbe electrolysis
- 2 December 1997
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 7 (23) , 2963-2966
- https://doi.org/10.1016/s0960-894x(97)10130-5
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Structure−Activity Relationships of Novel Hematoregulatory PeptidesJournal of Medicinal Chemistry, 1996
- Synthesis and Evaluation of Novel Substrates and Inhibitors of N-Succinyl-ll-diaminopimelate Aminotransferase (DAP-AT) from Escherichia coliJournal of the American Chemical Society, 1996
- An asymmetric synthesis of differentially protected meso-2,6-diaminopimelic acidTetrahedron Letters, 1994
- Asymmetric synthesis of 2,6-diaminopimelic acidsThe Journal of Organic Chemistry, 1992
- Asymmetric synthesis of differentially protected meso-2,6-diaminopimelic acidTetrahedron Letters, 1992
- Stereoselektive Synthese von (2S,6S)‐2,6‐Diaminoheptandisäure und von unsymmetrischen Derivaten der meso‐2,6‐DiaminoheptandisäureHelvetica Chimica Acta, 1992
- Synthesis of nonreducible bicyclic analogs of somatostatinJournal of the American Chemical Society, 1980
- Useful intermediates for synthesis of dicarba analogs of cystine peptides: selectively protected .alpha.-aminosuberic acid and .alpha.,.alpha.'-diaminosuberic acid of defined stereochemistryThe Journal of Organic Chemistry, 1980