Synthetic thiophane derivatives

ER Buchman, H Cohen

Index: Buchman; Cohen Journal of the American Chemical Society, 1944 , vol. 66, p. 847

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Citation Number: 4

Abstract

Kumler and Daniels' have suggested that the resonating form of the p-amino group with a separation of charge is a fundamental factor for the bacteriostatic activity of sulfanilamide type compounds. The experimental evidence for this suggestion is “that sulfanilamide has a higher (ultraviolet) extinction coefficient in base than in water.”*

A study of the tautomerism of 2-and 4-ethoxycarbonylthiolan-...

[DUUS, F. Tetrahedron, 1981 , vol. 37, # 15 p. 2633 - 2640]

A direction controlled Dieckmann type cyclization of half-th...

[Yamada, Yasuji; Ishii, Toshihide; Kimura, Masayuki; Hosaka, Kunio Tetrahedron Letters, 1981 , vol. 22, # 14 p. 1353 - 1354]

Synthesis of thiophenecarboxamides, thieno [3, 4-c] pyridin-...

[Shinkwin, Anne E.; Whish, William J. D.; Threadgill, Michael D. Bioorganic and Medicinal Chemistry, 1999 , vol. 7, # 2 p. 297 - 308]