From a Biogenetic Scenario to a Synthesis of the ABC Ring of Manzamine A
- 21 February 2002
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 67 (6) , 1890-1897
- https://doi.org/10.1021/jo0162033
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Reactions of Aminopentadienal Derivatives with 5,6-Dihydropyridinium Salts as an Approach to Manzamine Alkaloids Based upon Biogenetic ConsiderationsThe Journal of Organic Chemistry, 1999
- Selective Entry to the Dimeric or Oligomeric Pyridinium Sponge Macrocycles via Aminopentadienal Derivatives. Possible Biogenetic Relevance with Manzamine AlkaloidsJournal of the American Chemical Society, 1998
- BIOMIMETIC AND SYNTHETIC APPROACHES TO MARINE SPONGE ALKALOIDS DERIVED FROMBIS-PYRIDINE MACROCYCLES. A REVIEWOrganic Preparations and Procedures International, 1998
- Chapter Three 3-Alkylpiperidine alkaloids isolated from marine sponges in the order haploscleridaPublished by Elsevier ,1996
- 1,2,3,4-tetrahydro-8-hydroxymanzamines, alkaloids from two different haplosclerid spongesTetrahedron, 1994
- Manzamine A, a novel antitumor alkaloid from a spongeJournal of the American Chemical Society, 1986
- Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidineJournal of the American Chemical Society, 1986