Journal
JOURNAL OF SULFUR CHEMISTRY
Volume 37, Issue 1, Pages 54-60Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/17415993.2015.1089439
Keywords
Spiro heterocycles; isobenzofuran; 1; 3-thiazine; S-nucleophiles; carbamodithioates
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The reaction of 2-[3-oxo-isobenzofuran-1(3H)-ylidene]malononitrile, generated from phthalic anhydride and malononitrile, with ammonium alky(aryl)carbamodithioates, leading to the formation of functionalized spiro isobenzofuran-1,6'-[1,3] thiazine systems, in good yields, is reported. [GRAPHICS] Highlights The reaction of 2-[3-oxo-isobenzofuran-1(3H)-ylidene]malononi trile, with ammonium alky(aryl)carbamodithioates, leads to the formation of functionalized spiro isobenzofuran-1,6'-[1,3]thiazine systems, in good yields.
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