Synthesis of Diaminosuberic Acid Derivatives via Ring-Closing Alkyne Metathesis

This publication has 16 references indexed in Scilit:

• Asymmetric Synthesis of Differentially Protected 2,7-Diaminosuberic Acid, a Ring-Closure Metathesis Approach
  The Journal of Organic Chemistry, 1998
• Stereoselective Synthesis of meso-2,6-Diaminopimelic Acid and Its Selectively Protected Derivatives
  The Journal of Organic Chemistry, 1998
• Template-promoted dimerization of C-allylglycine: A convenient synthesis of (S,S)-2,7-diaminosuberic acid
  Tetrahedron Letters, 1998
• Synthesis of bis(α-amino acids) by palladium-catalyzed allylic double substitution
  Tetrahedron Letters, 1995
• Asymmetric synthesis of 2,6-diaminopimelic acids
  The Journal of Organic Chemistry, 1992
• Multiple metal carbon bonds. 35. A general route to tri-tert-butoxytungsten alkylidyne complexes. Scission of acetylenes by ditungsten hexa-tert-butoxide
  Organometallics, 1985
• Alkylation of Protected α-Amino Acid Derivatives in the Presence of Potassium Carbonate
  Synthesis, 1984
• Synthesis of nonreducible bicyclic analogs of somatostatin
  Journal 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 stereochemistry
  The Journal of Organic Chemistry, 1980
• The tungsten-tungsten triple bond. 8. Dinuclear alkoxides of tungsten(III) and structural characterization of hexaisopropoxybis(pyridine)ditungsten, the first compound with four-coordinated tungsten atoms united by a triple bond
  Inorganic Chemistry, 1979