@article { ISI:000360095900016,
	title = {Sulfuryl chloride promoted gem-dichlorination-dehydrochlorination in alkyl benzothiazinylacetates: synthesis of the skeleton of trichochrome pigments},
	journal = {Synthesis-Stuttgart},
	volume = {47},
	number = {17},
	year = {2015},
	month = {SEP},
	pages = {2631-2634},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Chemo- and stereoselective total synthesis of the basic trichochrome skeleton is described starting from o-aminothiophenol and maleic anhydride in very good overall yield. The process involves the synthesis of the corresponding 1,4-benzothiazin-2-ylacetates followed by their sulfuryl chloride induced dihalogenation-dehydrohalogenation and a second condensation with o-aminothiophenol as key steps.</p>},
	keywords = {condensations, halogenation, maleic anhydride, o-aminothiophenol, trichochrome framework},
	issn = {0039-7881},
	doi = {10.1055/s-0034-1378714},
	author = {Jangir, Ravi and Gadre, Smita R. and N. P. Argade}
}
