Iron-Catalyzed Aminolysis of β-Carbonyl 1,3-Dithianes: Synthesis of Stereodefined β-Enaminones and 3,4-Disubstituted Pyrazoles-Reference-Cited by-同舟云学术

Iron-Catalyzed Aminolysis of β-Carbonyl 1,3-Dithianes: Synthesis of Stereodefined β-Enaminones and 3,4-Disubstituted Pyrazoles

Published:2011-03-08 Issue:7 Volume:13 Page:1722-1725
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Yeming¹,Bi Xihe¹,Li Wei-Qi¹,Li Dehua¹,Zhang Qian¹,Liu Qun¹,Ondon Brim Stevy¹

Affiliation:

1. Department of Chemistry, Northeast Normal University, Changchun 130024, China, State Key Laboratory and Institute of Elemento-organic Chemistry, Nankai University, Tianjin 300071, China, and Physical Department, Harbin Institute of Technology, Harbin 150001, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol200246x

Reference46 articles.

1. Double Conjugate Addition of Dithiols to Propargylic Carbonyl Systems To Generate Protected 1,3-Dicarbonyl Compounds

2. On the synthesis of β-keto-1,3-dithianes from conjugated ynones catalyzed by magnesium oxide

3. Preparation of Protected β-Keto Aldehydes from β-Keto Esters via Selective Reduction of Acyl(alkoxycarbonyl)ketene Dithioacetals

4. Development of β-keto 1,3-dithianes as versatile intermediates for organic synthesis

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