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1,3-Dipolar cycloadditions of 2-ethoxy- and 2-(ethylthio)-1-azetines with nitrilimines

โœ Scribed by Abdul-Basset N. Luheshi; Robert K. Smalley; P.D. Kennewell; R. Westwood


Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
198 KB
Volume
31
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


I,3-Dipolar q&additions ofdiphenylnim%nines with 2&O-and2EtS-temmzethyi-I-azetines (la,b) are accompanied by ring-opening and loss of EtXH (LX = 0 or S) to give 1,2,4-triasoies (3), whereas with N-(4-nitrophenyl) nimXmines the qected cycloadducts andlor ring-opened products are formed.


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Unexpected 1,3-Dipolar Cycloaddition Rea
โœ Xiaofang Li; Haochong Liu; Bin Liu; Aiting Zheng; Guobin Li; Xianyong Yu; Pinggu ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 79 KB ๐Ÿ‘ 1 views

The 1,3-dipolar cycloaddition reactions of nitrilimine with thiazolo[3,2-a]pyrimidine derivatives was investigated. Bis-cycloadducts were obtained through a domino 1,3-dipolar cycloaddition/ring-opening/ring-opening/ 1,3-dipolar cycloaddition processes. The structures of the products were characteri