1448883-47-3Relevant academic research and scientific papers
Synthesis of spirooxindoles bearing 2,3-(or 2,5-)dihydrothiophene-2-thione moiety via [3+2] annulation of carbon disulfide with Morita-Baylis-Hillman carbonates of isatins
Min, Beom Kyu,Kim, Gieun,Roh, Hwa Jung,Seo, Da Young,Kim, Jae Nyoung
, p. 1674 - 1678 (2018)
Various spirooxindoles bearing 2,3-(or 2,5-)dihydrothiophene-2-thione moiety have been synthesized via [3+2] annulation reaction of carbon disulfide and the nitrogen ylides derived from Morita-Baylis-Hillman carbonates of isatins. 2,3-Dihydro- and 2,5-dih
Baylis-Hillman carbonates in organic synthesis: A convenient one-pot strategy for nitrone-spiro-oxindole frameworks
Basavaiah, Deevi,Badsara, Satpal Singh,Veeraraghavaiah, Gorre
, p. 7995 - 8001 (2013/08/23)
A facile one-pot protocol for synthesis of nitrone-spiro-oxindole frameworks via alkylation of nitromethane with carbonates of Baylis-Hillman alcohols, derived from isatins and cyclohex-2-enone derivatives, followed by reductive cyclization is described.
