A facile synthesis of the 4-aza-analogs of 1-arylnaphthalene lignans chinensin, justicidin B, and Taiwanin C
- 1 December 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (48) , 8295-8296
- https://doi.org/10.1016/s0040-4039(97)10204-0
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Antiplatelet Arylnaphthalide Lignans from Justicia procumbensJournal of Natural Products, 1996
- A New Approach to the 1-Arylnaphthalene Lignans Utilizing a Tandem Pummerer-Diels-Alder Reaction SequenceThe Journal of Organic Chemistry, 1995
- New, short synthesis of arylnaphthofuranone lignans based on reactions of o-aroylbenzyllithiums with furan-2(5H)-oneJournal of the Chemical Society, Perkin Transactions 1, 1995
- Facile construction of the 1-phenylnaphthyl skeleton via an ester-mediated nucleophilic aromatic substitution reaction. Applications to the synthesis of phenylnaphthalide lignansJournal of the Chemical Society, Perkin Transactions 1, 1995
- A rapid entry into podophyllotoxin congeners: Synthesis of justicidin BTetrahedron Letters, 1994
- Justicidin E: A new leukotriene biosynthesis inhibitor.Bioorganic & Medicinal Chemistry Letters, 1993
- A concise synthesis of taiwanin E using a michael initiated ring closure protocolTetrahedron Letters, 1991
- The Antiviral Action of LignansPlanta Medica, 1989
- Justicidin B, a Cytotoxic Principle from Justicia pectoralisJournal of Natural Products, 1988
- Justicidin B, a Bioactive Trace Lignan from the Seeds of Sesbania drummondiiJournal of Natural Products, 1986