Computer-assisted design and lactonization of model seco-acid derivatives of lankanolide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. The first stereoselective total synthesis of lankanolide. Part 1: Computer-assisted design and lactonization of model seco-acid derivatives
2. Stoffwechselprodukte von Actinomyceten. 21. Mitteilung. Lankamycin und Lankacidin
3. Stoffwechselprodukte von Mikroorganismen. 103. Mitteilung [1]. Zur Stereochemie des Lankamycins
4. Stereocontrolled synthesis of lankanolide from 1,6-anhydro-β-d-glucopyranose (levoglucosan): 1, synthesis of the C-1/7 and C-8/15 segments
5. Further Studies on the Anti-Selective Aldol Reaction of Chiral Imides
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1. An Adventurous Synthetic Journey with MNBA from Its Reaction Chemistry to the Total Synthesis of Natural Products;Bulletin of the Chemical Society of Japan;2014-02-15
2. Chemical Applications of Fluorous Reagents and Scavengers;Topics in Current Chemistry;2011
3. Evaluation of the Efficiency of the Macrolactonization Using MNBA in the Synthesis of Erythromycin A Aglycon;The Chemical Record;2009-12-25
4. New Development of Photo-induced Electron Transfer Reaction and Total Synthesis of Natural Product;YAKUGAKU ZASSHI;2005-01-01
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