Synthesis of the chiral (8S)-7-aza-1,3(E),9-decatriene system from natural .alpha.-amino acids and its intramolecular Diels-Alder reaction directed toward chiral trans-hydroisoquinolones
- 1 August 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 54 (17) , 4114-4120
- https://doi.org/10.1021/jo00278a024
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- A synthesis of protected aminoalkyl epoxides from .alpha.-amino acidsThe Journal of Organic Chemistry, 1987
- Stereocontrolled synthesis of cis-fused hydroisoquinolines by an intramolecular Diels-Alder reaction of (Z)-dienesThe Journal of Organic Chemistry, 1985
- On the double bond isostere of the peptide bond: preparation of modified di- and tri-peptides incorporating proline and alanine analoguesJournal of the Chemical Society, Perkin Transactions 1, 1984
- The IntramolecularDiels–Alder ReactionPublished by Wiley ,1984
- On the double bond isostere of the peptide bond: preparation of an enkephalin analogueJournal of the Chemical Society, Perkin Transactions 1, 1982
- Congeners of the .alpha. conformer of dopamine derived from octahydrobenz[h]isoquinolineJournal of Medicinal Chemistry, 1980