4.1 Article

A synthesis of functionalized spiro isobenzofuran-1,6′-[1,3] thiazines from phthalic anhydride-malononitrile adduct and ammonium carbamodithioates

Journal

JOURNAL OF SULFUR CHEMISTRY
Volume 37, Issue 1, Pages 54-60

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/17415993.2015.1089439

Keywords

Spiro heterocycles; isobenzofuran; 1; 3-thiazine; S-nucleophiles; carbamodithioates

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available