Synthesis of Termini-Differentiated 6-Carbon Stereotetrads: An Alkylative Oxidation Strategy for Preparation of the C21−C26 Segment of Apoptolidin1
Author:
Affiliation:
1. Department of Chemistry, Purdue University, West Lafayette, Indiana 47907
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol026377m
Reference20 articles.
1. Asymmetric Epoxy Cyclohexenyl Sulfones: Readily Accessible Progenitors of Stereodefined Six-Carbon Arrays1
2. Synthesis of 6-carbon termini-differentiated stereotriads via symchiral 2-trifloxy-1,3-cyclohexadiene monoepoxide
3. Scope and limitations in the Jacobsen epoxidation of dienyl sulfones
4. An efficient and convenient synthesis of enantiopure 4-(t-butyldimethylsilyloxy)-cyclohex-2-en-1-one: a formal synthesis of (±)-mesembranol
5. Syntheses of Highly Substituted Enantiopure C6 and C7 Enones1
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