Construction of all O-alkoxy D-tetrose and D-pentose stereoisomers from 2,3-O-isopropylidene-D-glyceraldehyde using 2-(trimethylsilyl)thiazole as a formyl anion equivalent

DOI: 10.1055/s-1992-34170

Source and publish data:

Synthesis p. 201 - 210 (1992)

Update date:2022-08-02

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Authors:

Dondoni Dondoni

Orduna Orduna

Merino Merino

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Article abstract of DOI:10.1055/s-1992-34170

All D-tetroses and D-pentoses having differentially protected hydroxy groups are synthesized by an iterative one-carbon chain-elongation cycle commencing with the addition of 2-(trimethylsilyl)thiazole to 2,3-O-isopropylidene-D-glyceraldehyde. One half of

Full text of DOI:10.1055/s-1992-34170

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