Jianwei Dou

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Name:
Organization: Xi’an Jiaotong University
Department: Department of Chemistry, School of Science, and College of Pharmacy
Title:
Co-reporter:Silong Xu, Shaoying Zhu, Jian Shang, Junjie Zhang, Yuhai Tang, and Jianwei Dou
The Journal of Organic Chemistry 2014 Volume 79(Issue 8) pp:3696-3703
Publication Date(Web):March 25, 2014
DOI:10.1021/jo500375q
A catalyst-free allylic alkylation of stabilized phosphorus ylides with allylic carbonates via a regioselective SN2′ process is presented. Subsequent one-pot Wittig reaction with both aliphatic and aromatic aldehydes as well as ketenes provides structurally diverse skipped dienes (1,4-dienes) in generally high yields and moderate to excellent stereoselectivity with flexible substituent patterns. This one-pot SN2′ allylation–Wittig strategy constitutes a convenient and efficient synthetic method for highly functionalized skipped dienes from readily available starting materials.
Benzenepropanoic acid, β-[[(1,1-dimethylethoxy)carbonyl]oxy]-4-methyl-α-methylene-, ethyl ester
Benzenepropanoic acid, 4-chloro-β-[[(1,1-dimethylethoxy)carbonyl]oxy]-α-methylene-, ethyl ester
Benzenepropanoic acid, β-[[(1,1-dimethylethoxy)carbonyl]oxy]-α-methylene-, methyl ester
Benzenepropanoic acid, β-[[(1,1-dimethylethoxy)carbonyl]oxy]-α-methylene-, ethyl ester
Ethyl 2-((4-fluorophenyl)amino)-4-methylthiazole-5-carboxylate
2-Propenoic acid, 2-[[[(1,1-dimethylethoxy)carbonyl]oxy]methyl]-, ethyl ester
2-Furanpropanoic acid, b-hydroxy-a-methylene-, ethyl ester
Pentanoic acid, 3-hydroxy-2-methylene-, ethyl ester