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SRN1 Reactions in the Nitrobenzo[1,3]dioxole Series.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
J. Meuche-Albeny +3 more
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2001
[37635-87-3] C3H2O2S (MW 102.12) InChI = 1S/C3H2O2S/c6-3-4-1-2-5-3/h1-2H InChIKey = MMGCXSBBWCOBEX-UHFFFAOYSA-N (dienophile in Diels–Alder reactions;1 acetylene equivalent in cycloaddition reactions;2 source of ketene;3 forms dication dichalcogenides with strong Lewis acids4) Alternate Name: vinylene thionocarbonate.
openaire +1 more source
[37635-87-3] C3H2O2S (MW 102.12) InChI = 1S/C3H2O2S/c6-3-4-1-2-5-3/h1-2H InChIKey = MMGCXSBBWCOBEX-UHFFFAOYSA-N (dienophile in Diels–Alder reactions;1 acetylene equivalent in cycloaddition reactions;2 source of ketene;3 forms dication dichalcogenides with strong Lewis acids4) Alternate Name: vinylene thionocarbonate.
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On the Cationic Polymerization of 2,2-Dimethyl-1,3-dioxole and 2,2-Diphenyl-1,3-dioxole
Macromolecules, 1979M. K. Akkapeddi, H. K. Reimschuessel
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“New route to 2,2-difluoro-1,3-dioxoles”
199311th Winter Conference, St.Petersburg, USA (1993).
NAVARRINI, WALTER MAURIZIO +3 more
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The Preparation of 1,3-Dioxole and 2,2-Dimethyl-1,3-dioxole
Journal of the American Chemical Society, 1961openaire +1 more source

