X=Y-ZH systems as potential 1,3-dipoles
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 44 (23) , 7271-7282
- https://doi.org/10.1016/s0040-4020(01)86099-3
Abstract
No abstract availableThis publication has 45 references indexed in Scilit:
- X=Y-ZH Systems as potential 1,3-dipolesTetrahedron, 1988
- XY–ZH systems as potential 1,3-dipoles. Part 10. The decarboxylative route to azomethine ylides. Background and relevance to pyridoxal decarboxylasesJournal of the Chemical Society, Perkin Transactions 1, 1988
- The decarboxylative route to azomethine ylides. Stereochemistry of 1,3-dipole formationJournal of the Chemical Society, Chemical Communications, 1987
- The decarboxylative route to azomethine ylides. Mechanism of 1,3-dipole formationJournal of the Chemical Society, Chemical Communications, 1987
- XY–ZH Systems as potential 1,3-dipoles. Part 8. Pyrrolidines and Δ5-pyrrolines (3,7-diazabicyclo[3.3.0]octenes) from the reaction of imines of α-amino acids and their esters with cyclic dipolarophiles. Mechanism of racemisation of α-amino acids and their esters in the presence of aldehydesJournal of the Chemical Society, Perkin Transactions 1, 1986
- A new perspective on pyridoxal chemistry and its relevance to enzyme inhibitionBiochemical Society Transactions, 1986
- Decarboxylative transamination. A new route to spirocyclic and bridgehead-nitrogen compounds. Relevance to α-amino acid decarboxylasesJournal of the Chemical Society, Chemical Communications, 1984
- Decarboxylative transamination. Mechanism and applications to the synthesis of heterocyclic compoundsJournal of the Chemical Society, Chemical Communications, 1984
- Stereochemistry of pyridoxal phosphate catalyzed enzyme reactionsAccounts of Chemical Research, 1980
- DEAMINATION OF SERINEPublished by Elsevier ,1952