ArticleThe Journal of organic chemistry2007
Synthesis of aza-analogues of the glycosylated tyrosine portion of mannopeptimycin-E.
Article in The Journal of organic chemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Comprehensive review of chemical strategies for the preparation of new aminoglycosides and their biological activities.Chemical Society reviews · 2018Review
- Functionalization of protected tyrosine via Sonogashira reaction: synthesis of 3-(1,2,3-triazolyl)-tyrosine.Molecular diversity · 2016Article
- A Survey of Recent Synthetic Applications of 2,3-Dideoxy-Hex-2-enopyranosides.Molecules (Basel, Switzerland) · 2015Review
- De novo synthesis and biological evaluation of C6″-substituted C4″-amide analogues of SL0101.Organic letters · 2014Article
- Merremoside D: de novo synthesis of the purported structure, NMR analysis, and comparison of spectral data.Organic letters · 2014Article
- Article
- De Novo Asymmetric Syntheses of d-, l- and 8-epi-Swainsonine.Tetrahedron · 2008Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Two C4' amido disaccharide analogues of mannopeptimycin-E were synthesized via an iterative palladium glycosylation sequence. The stereoselective synthesis of the C4' acylated 1,4-alpha,alpha-manno,manno-amido disaccharide has been achieved in ten steps from a protected d-tyrosine. The path relies upon a regio- and diastereoselective palladium-catalyzed azide substitution reaction. The competence of the synthesis is demonstrated by the good overall yield (21%) from protected tyrosine.
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