Diastereoselective additions of allylmetal reagents to free and protected syn-α,β-dihydroxyketones enable efficient synthetic routes to methyl trioxacarcinoside A

Organic Letters

Volumn 14, Issue 7, 2012, Pages 1812-1815

  Smaltz, Daniel J ^a   Švenda, Jakub ^a   Myers, Andrew G ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHELATING AGENT; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; GLYCOSIDE; KETONE; METHYL TRIOXACARCINOSIDE A;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

CHELATING AGENTS; GLYCOSIDES; INDICATORS AND REAGENTS; KETONES; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 84859575146     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol300377a     Document Type: Article

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