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Use of olefin cross-metathesis to release azide-containing sugars from solid support.

Organic letters (2003-11-25)
Takuya Kanemitsu, Peter H Seeberger
RESUMEN

[reaction: see text] The octenediol linker used during automated oligosaccharide assembly is cleaved by olefin cross-metathesis. Until now, this linker could not be applied to sugars containing azides. A detailed study of the cleavage reaction served as basis for the development of a new protocol using the [(H(2)Imes)(3-Br-py)(2)(Cl)(2)Ru=CHPh] catalyst and 1-pentene. Efficient release of azide-protected carbohydrates from solid support can be readily achieved.

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Sigma-Aldrich
[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(benzylidene)bis(3-bromopyridine)ruthenium(II)
Sigma-Aldrich
1-Pentene, ≥98.5% (GC)
Sigma-Aldrich
1-Pentene, 98%
Supelco
1-Pentene, analytical standard