79043-40-6Relevant academic research and scientific papers
Rearrangement Products of α-Salicylidene-γ-thiobutyrolactones
Miller, Gerald A.,Heindel, Ned D.
, p. 4751 - 4753 (1981)
A convenient means of condensing various salicylaldehydes with γ-thiobutyrolactone has been found.The condensation, which is accompanied by a rearrangement, yields either a product of Michael-additive cyclization (a 2,3,3a,9b-tetrahydrothienocoumarin) or one of oxidation (the disulfide of a 3-(2-mercaptoethyl)coumarin).
