Journal of Organic Chemistry p. 116 - 122 (1984)
Update date:2022-08-04
Topics:
Press, Jeffery B.
Eudy, Nancy H.
5-Aryl-3,4-dihydro-2H-1,6-benzothiazocines (1) were prepared in a two-step sequence from o-aminothiophenols (2) and γ-halobutyrophenones (3); 3a-aryl-1,2,3,3a-tetrahydropyrrolo<2,1-b>benzothiazoles (4) formed if the reaction was run in one step.Imine 1 co
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(1984)Doi:10.1134/S1070428006070335
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