Selective reduction and cleavage of the N-N bond of fused tetrahydropyridazines: a route to functionalised lactams
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (14) , 1573-1575
- https://doi.org/10.1016/s0040-4039(01)81045-5
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Total syntheses of (±) aminoallose derivativesTetrahedron Letters, 1986
- Zwei Strategien, ein Ziel: SwainsoninNachrichten aus Chemie, Technik und Laboratorium, 1986
- Hetero-Diels-Alder reaction in highly functionalized natural product synthesisAccounts of Chemical Research, 1986
- Stereospecific total synthesis of (.+-.)-gephyrotoxin 223ABJournal of the American Chemical Society, 1985
- De novo-synthesis of carbohydrates preparation of 4-amino-4-deoxy-Tetrahedron Letters, 1984
- The isoxazoline route to the molecules of natureAccounts of Chemical Research, 1984
- Total synthesis of (.+-.)-saxitoxinJournal of the American Chemical Society, 1984
- Isoxazolines‐Key Intermediates For Syntheses of Some Naturally Occuring Amino CompoundsBulletin des Sociétés Chimiques Belges, 1983
- Intramolecular Cycloaddition Reactions ofin situGenerated Azoalkenes; Synthesis of Pyrrolo[1,2-b]pyridazine Derivatives from α-Haloketone 4-PentenoylhydrazonesSynthesis, 1983
- Alkaloids from nitronesAccounts of Chemical Research, 1979