Simultaneous 1,2-, 1,3- and 1,4-addition of trithiazyl trichloride to a conjugated diene
Charles W. Rees, Tai‐Yuen Yue
Abstract
Charles W. Rees, Tai‐Yuen Yue
Abstract
1,4-Diphenylbuta-1,3-diene and trithiazyl trichloride 1 react to give a bi(thiadiazole) 2, an isothiazoloisothiazole 3, a dithiazolothiazine 4 and the thiazinodithiatriazepines 5 and 6, all of which could arise from initial addition of the trimer 1, or its monomer, to the conjugated diene by 1,2-,1,4- and, for the first time to an all-carbon diene, 1,3-(‘criss-cross’) cycloaddition reactions.
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1,4-Diphenylbuta-1,3-diene and trithiazyl trichloride 1 react to give a bi(thiadiazole) 2, an isothiazoloisothiazole 3, a dithiazolothiazine 4 and the thiazinodithiatriazepines 5 and 6, all of which could arise from initial addition of the trimer 1, or its monomer, to the conjugated diene by 1,2-,1,4- and, for the first time to an all-carbon diene, 1,3-(‘criss-cross’) cycloaddition reactions.
Key concepts: Diene, Trimer, Conjugated diene, Conjugated system, Monomer, Cycloaddition, Chemistry, Medicinal chemistry