An enantioselective approach to ring a of taxol using the wieland-miescher ketone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. A new and practical approach to the synthesis of taxol and taxol analogs: the pinene path.
2. TAXANE DITERPENE SYNTHESIS STRATEGIES. A REVIEW
3. A straightforward route to functionalized intermediates containing the CD substructure of taxol.
4. New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures
5. Synthesis and conversion of 2-methyl-2-(3-oxobutyl)-1,3-cyclopentanedione to the isomeric racemic ketols of the [3.2.1]bicyclooctane and of the perhydroindane series
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1. The Wieland-Miescher Ketone: A Journey from Organocatalysis to Natural Product Synthesis;Synlett;2011-12-09
2. Traces of Water as a Key Parameter for the Formation of an Epoxydithio Compound;Synlett;2007-06
3. One-Pot Conversion of Glycals to cis-1,2-Isopropylidene-α-glycosides;The Journal of Organic Chemistry;2003-08-26
4. Efficient and selective catalytic oxidative cleavage of α-hydroxy ketones using vanadium-based HPA and dioxygen;Chemical Communications;2001
5. Ring A building blocks for taxoids and taxamycins;Canadian Journal of Chemistry;1997-09-01
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