The first total synthesis of calabricoside A
β Scribed by Yuguo Du; Guohua Wei; Robert J. Linhardt
- Book ID
- 104254292
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 164 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Quercetin 3-O-[a-L-rhamnopyranosyl-(12)-a-L-arabinopyranoside]-7-O-b-D-glucopyranoside (calabricoside A), a new flavonol triglycoside isolated from the aerial parts of Putoria calabrica showing strong radical scavenging activity, was synthesized through a combination of phase-transfer-catalyzed C-3 glycosylation and AgOTf promoted homogeneous C-7 glycosylation in CH 2 Cl 2 .
π SIMILAR VOLUMES
Total synthesis of mauritine-A is accomplished featuring a key cycloetherification reaction based on an intramolecular S N Ar reaction.
A highly convergent asymmetric total synthesis of emericellamide A, a 19-membered antibacterial depsipeptide isolated from the co-culture of an Emericella sp. (strain CNL-878) and a Salinispora arenicola (strain CNH-665) is described.