Efficient and mild synthesis of functionalized 2,3-dihydrofuran derivatives via domino reaction in water

Tetrahedron Letters

Volumn 52, Issue 18, 2011, Pages 2379-2382

  Xie, Jian Wu ^a   Li, Ping ^a   Wang, Ting ^a   Zhou, Fei Ting ^a  

^a ZHEJIANG NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; BENZOPYRAN DERIVATIVE; FURAN DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; MICHAEL ADDITION; NONHUMAN; REACTION TIME; STEREOCHEMISTRY; SYNTHESIS;

EID: 79953269218     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.02.093     Document Type: Article

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60. 6 + Na 362.06382, found 362.06375.
61. For example, compound 3ca [6.16 (d, J = 1.82 Hz, 1H), 4.85 (d, J = 1.22 Hz, 1H)] exhibited coupling constants (J) data identical to that reported in the literature [Compound 4ca 6.17 (d, J = 1.8 Hz, 1H), 4.86 (d, J = 1.2 Hz, 1H); (J. Org. Chem. 2010, 75, 8716]. Diastereoselectivity (3ca) was also determined by HPLC analysis on chiral Chiralpak columns and the HPLC data was identical to that reported in the literature (4ca, J. Org. Chem. 2010, 75, 8716).
62. -3.