Unexpectedly convenient and stereoselective synthesis of 4α-acyloxy-2-chloropodophyllotoxins in the presence of BF 3·Et 2O

Bioorganic and Medicinal Chemistry Letters

Volumn 21, Issue 13, 2011, Pages 4008-4012

  Xu, Hui ^a   Xiao, Xiao ^a   Zhao, Xue Fei ^b   Guo, Yong ^a   Yao, Xiao Jun ^b  

^a NORTHWEST A F UNIVERSITY   (China)

^b LANZHOU UNIVERSITY   (China)

Author keywords

2 Chloropodophyllotoxin; 4 Acyloxy 2 chloropodophyllotoxin; Insecticidal activity; Podophyllotoxin; Stereoselective

Indexed keywords

4ALPHA ACYLOXY 2 CHLOROPODOPHYLLOTOXIN DERIVATIVE; CARBOXYLIC ACID; INSECTICIDE; PODOPHYLLOTOXIN; PODOPHYLLOTOXIN DERIVATIVE; TOOSENDANIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CONTROLLED STUDY; ESTERIFICATION; INSECTICIDAL ACTIVITY; NONHUMAN; STEREOCHEMISTRY; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

ACYLATION; ANIMALS; BORANES; CHLORINE; INSECTICIDES; LARVA; MOLECULAR STRUCTURE; MOTHS; PODOPHYLLOTOXIN; STEREOISOMERISM; TIME FACTORS;

MYTHIMNA SEPARATA;

EID: 79958699204     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2011.05.004     Document Type: Article

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