A new total synthesis of (±) steganone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Application de la reaction d'ulimann a la synthese de diaryles encombres precurseurs de lignanes bis-benzocyclootadieniques
2. Synthesis of (±)-podorhizone via intermediate α-hydroxyalkylation of a β-benzyl γ-butyrolactone
3. A new route to the bis-benzocyclooctadiene lignan skeleton: Total syntheses of (±) picrostegane, (±) isopicrostegane and (±) isostegane
4. Total synthesis of (+-)-steganacin
5. Total synthesis of the antileukaemic lignan (±)-steganacin
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1. Transition-Metal-Free Synthesis of a Known Intermediate in the Formal Synthesis of (-)-Steganacin;European Journal of Organic Chemistry;2016-12-23
2. A Concise Atroposelective Formal Synthesis of (-)-Steganone;European Journal of Organic Chemistry;2014-08-21
3. Copper-Mediated Aryl-Aryl Bond Formation Leading to Biaryls: A Century after the Ullmann Breakthrough;Copper-Mediated Cross-Coupling Reactions;2013-10-04
4. Progress in the Syntheses of Dibenzocyclooctadiene Lignans;Studies in Natural Products Chemistry;2013
5. Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products;Chemical Reviews;2010-10-12
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