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(2r,3r)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate  (Enamine Ltd)


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    Enamine Ltd (2r,3r)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate
    (2r,3r) 5,7 Dihydroxy 2 (3,4,5 Trihydroxyphenyl) 3,4 Dihydro 2h 1 Benzopyran 3 Yl 3,4,5 Trihydroxybenzoate, supplied by Enamine Ltd, used in various techniques. Bioz Stars score: 99/100, based on 239 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/2r/(2R%2C3R)-5%2C7-dihydroxy-2-(3%2C4%2C5-trihydroxyphenyl)-3%2C4-dihydro-2H-1-benzopyran-3-yl+3%2C4%2C5-trihydroxybenzoate/custom%40en300-7403305%4042680304
    Average 99 stars, based on 239 article reviews
    (2r,3r)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-3-yl 3,4,5-trihydroxybenzoate - by Bioz Stars, 2026-09
    99/100 stars

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    Transformation Assay:

    Article Title: Exceptional isolation of both imine and enamine desmotropes of 4,1-benzothiazepines
    Article Snippet: The desmotropy of differently substituted (R*)-3-ethoxycarbonyl-2-aryl-3,5-dihydro-4,1-benzothiazepines and 3-ethoxycarbonyl-2-aryl-1,5-dihydro-4,1-benzothiazepines was investigated.. The target 4,1-benzothiazepines were obtained via the ring transformation of (2R*,2aS*)-2-chloro-2a-aryl-2,2adihydro-2H,4H-azeto[1,2-a][3,1]benzothiazin-1-ones with sodium ethoxide in ethanol.. The b-amino ester intermediate of the ring-enlargement reaction was isolated.



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