Fulvenes derived from illudin S
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Fungal Metabolites. The Structures of the Novel Sesquiterpenoids Illudin-S and -M
2. Illudin s (lampterol)
3. Structure of lampterol (illudin S)
4. The absolute configuration of illudin S; application of the dibenzoate chirality rule
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1. Total Synthesis of the Sesquiterpene (±)-Illudin C via an Intramolecular Nitrile Oxide Cycloaddition;Organic Letters;2001-07-06
2. Anti-leukemic action of the novel agent MGI 114 (HMAF) and synergistic action with topotecan;Leukemia;2000-01
3. Discovery and development of sesquiterpenoid derived hydroxymethylacylfulvene: a new anticancer drug;Bioorganic & Medicinal Chemistry;1999-05
4. An Approach toward the Illudin Family of Sesquiterpenes Using the Tandem Cyclization−Cycloaddition Reaction of Rhodium Carbenoids;The Journal of Organic Chemistry;1997-03-01
5. Acylfulvenes, a new class of potent antitumor agents;Experientia;1996-01
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