Efficient and mild synthesis of highly substituted 2,5-dihydrofuran and furan derivatives via stepwise reaction

Tetrahedron

Volumn 67, Issue 19, 2011, Pages 3476-3482

  Wang, Tiantian ^a   Liu, Jia ^a   Lv, Zhiliang ^a   Zhong, Hanyu ^a   Chen, Huan ^a   Niu, Chunjuan ^a   Li, Ke ^a  

^a SECOND MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

2,5 Dihydrofuran; Anti tumor; Furan; Selective synthesis; Stepwise reaction

Indexed keywords

2 (3,4,5 TRIMETHOXYPHENYL) 4 VINYL 2,5 DIHYDROFURAN 3 CARBOXYLIC ACID; ALKYL GROUP; FLUOROURACIL; FURAN DERIVATIVE; MALONIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CONTROLLED STUDY; CRYSTAL STRUCTURE; HELA CELL; HUMAN; HUMAN CELL; IN VITRO STUDY; ONE POT SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS; TEMPERATURE DEPENDENCE; TIME; X RAY CRYSTALLOGRAPHY;

EID: 79954998480     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2011.03.038     Document Type: Article

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