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2008 Multi-membered O,N,S-heterocycles R 0692 Macrocyclic Compounds from Benzenedithiols and Triazine: Modification of Tetrathiacalix[4]arene. — The synthesis of the macrocyclic compounds (I) having benzenedithionate and triazine moieties is achieved by an efficient fragment coupling approach. In the solid state, they adopt 1,3-alternate conformations. Combination of two pairs of electron rich and electron poor units, and ortho-ortho and/or ortho-meta connections of sulfur atoms with aromatic carbons are novel features of the macrocy- cles. — (ALAM, A.; YAMAGUCHI, M.; YAMAMOTO, T.; NAKAJO, S.; OGAWA, S.; SATO*, R.; J. Heterocycl. Chem. 45 (2008) 2, 461-465; Dep. Chem. Eng., Fac. Eng., Iwate Univ., Ueda, Morioka 020, Japan; Eng.) — H. Haber 30- 169

ChemInform Abstract: Macrocyclic Compounds from Benzenedithiols and Triazine: Modification of Tetrathiacalix[4]arene

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Page 1: ChemInform Abstract: Macrocyclic Compounds from Benzenedithiols and Triazine: Modification of Tetrathiacalix[4]arene

2008

Multi-membered O,N,S-heterocyclesR 0692 Macrocyclic Compounds from Benzenedithiols and Triazine: Modification of

Tetrathiacalix[4]arene. — The synthesis of the macrocyclic compounds (I) having benzenedithionate and triazine moieties is achieved by an efficient fragment coupling approach. In the solid state, they adopt 1,3-alternate conformations. Combination of two pairs of electron rich and electron poor units, and ortho-ortho and/or ortho-meta connections of sulfur atoms with aromatic carbons are novel features of the macrocy-cles. — (ALAM, A.; YAMAGUCHI, M.; YAMAMOTO, T.; NAKAJO, S.; OGAWA, S.; SATO*, R.; J. Heterocycl. Chem. 45 (2008) 2, 461-465; Dep. Chem. Eng., Fac. Eng., Iwate Univ., Ueda, Morioka 020, Japan; Eng.) — H. Haber

30- 169