86030-95-7

Upstream product

• 73541-95-4 methyl 3,4-anhydro-2-deoxy-6-O-(triphenylmethyl)-α-D-ribo-hexopyranoside 
• 86030-92-4 methyl 2,4-dideoxy-6-O-(triphenylmethyl)-α-D-erythro-hexopyranoside 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 94371-04-7 methyl 2,4-dideoxy-6-O-(phenylmethyl)-α-D-erythro-hexopyranoside 
• 94480-29-2 (2S)-2-benzyloxymethyl-2,3-dihydro-4H-pyran-4-one 
• 94371-08-1 (5S)-5-(Hydroxymethyl)-3-<(1,3-dioxolan-2-yl)methyl)>-4,5-dihydroisoxazole 
• 90344-31-3 (5S)-5-<(4R)-(2,2-dimethyl-1,3-dioxolan-4-yl)>-3-<(1,3-dioxolan-2-yl)methyl>-4,5-dihydroisoxazole 
• 82891-99-4 ethylene ketal of 3-nitropropanal 
• 94371-09-2 methyl 3-O-(tert-butyldiphenylsilyl)-2,4-dideoxy-6-O-(phenylmethyl)-α-D-erythro-hexopyranoside 
• 86030-93-5 tert-Butyl-((2S,4R,6S)-2-methoxy-6-trityloxymethyl-tetrahydro-pyran-4-yloxy)-diphenyl-silane 
• 94480-27-0 (5S)-5-<(phenylmethoxy)methyl>-3-<(1,3-dioxolan-2-yl)methyl>-4,5-dihydroisoxazole 
• 94480-28-1 (S)-5-Benzyloxy-1-[1,3]dioxolan-2-yl-4-hydroxy-pentan-2-one 
• 94480-26-9 (2S,6S)-tetrahydro-2-methoxy-6-<(phenylmethoxy)methyl>-4H-pyran-4-one 
• 94371-07-0 (5S)-5-<(1R)-1,2-dihydroxyethyl>-3-<(1,3-dioxolan-2-yl)methyl>-4,5-dihydroisoxazole 

Downstream Products

• 86030-94-6 methyl 3-O-(tert-butyldiphenylsilyl)-2,4-dideoxy-β-D-erythro-hexopyranoside 
• 132674-39-6 [(2S,4R,6S)-2-((2R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxymethyl)-6-methoxy-tetrahydro-pyran-4-yloxy]-tert-butyl-diphenyl-silane 
• 132674-38-5 [(2S,4R,6S)-2-((2S,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxymethyl)-6-methoxy-tetrahydro-pyran-4-yloxy]-tert-butyl-diphenyl-silane 

Relevant academic research and scientific papers

A Nitrile Oxide Based Entry to 2,3-Dihydropyran-4-ones. Synthesis of a Protected Version of "Compactin Lactone" in Racemic and Optically Active Forms

The use of nitrile oxides bearing a masked β-oxo group as β-hydroxy-3-oxopropionylating agents for the vicinal functionalization of olefins is described.The β-hydroxy ketones revealed on hydrogenation of the initially formed 1,3-dipolar cycloaddition prod

MEVINIC ACIDS AND ANALOGUES: PREPARATION OF A KEY CHIRAL INTERMEDIATE

The preparation of methyl 3-O-tert-butyldiphenylsilyl-2,4-dideoxy-β-D-erytrohexopyranoside, a key chiral intermediate for mevinic acids, and its elaboration into four mevinate analogues are described.