1,3-Dithioles
作者： P. Bałczewski , W. Kudelska , A. Bodzioch
DOI: 10.1016/B978-008044992-0.00412-0
关键词:
摘要: This chapter deals with the synthesis, reactivity, and characterization of five-membered heterocycles containing two sulfur atoms in positions 1 3 ring, that is, 1,3-dithiolylium ions, mesoionic 1,3-dithiol-4-ones 4-thiones, 1,3-dithioles, 1,3-dithiolanes. Aspects reactivity 1,3-dithiole derivatives concern all synthetic manipulations at ring carbon heteroatoms as well substituents attached to these atoms. A large section is devoted tetrathiafulvalenes (TTFs) a special subclass 1,3-dithioles π-extended TTFs, due great interest material sciences compounds, mainly semiconductors, organic metals, superconductors, progress made their investigations. New applications medicine, bioorganic enzymatic chemistry are also discussed. An emphasis put on theoretical experimental methods new procedures for 1,3-dithiolane protection deprotection carbonyl groups, which have been developed reviewed period.
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sci-hub.se 参考文章(795)
Richard W. Fitch, Xue-Feng Pei, Yumika Kaneko, Tara Gupta, Dan Shi, Irina Federova, John W. Daly, Homoepiboxidines Bioorganic & Medicinal Chemistry. ,vol. 12, pp. 179- 190 ,(2004) , 10.1016/J.BMC.2003.10.015
Gregory L. Garrison, K. Darrell Berlin, Benjamin J. Scherlag, Ralph Lazzara, Eugene Patterson, Tamas Fazekas, Subbiah Sangiah, Chun-Lin Chen, F. D. Schubot, Dick van der Helm, Novel 3,7-diheterabicyclo[3.3.1]nonanes that possess predominant class III antiarrhythmic activity in 1-4 day post infarction dog models: X-ray diffraction analysis of 3-[4-(1H-imidazol-1-yl)benzoyl]-7-isopropyl-3,7-diazabicyclo[3.3.1]nonane dihydroperchlorate Journal of Medicinal Chemistry. ,vol. 39, pp. 2559- 2570 ,(1996) , 10.1021/JM950772J
Paulo Afonso de Almeida, Tänia Maria Sarmento da Silva, Aurea Echevarria, MESOIONIC 5-ALKYL-1,3-DITHIOLIUM-4-THIOLATES: SYNTHESIS AND BRINE SHRIMP TOXICITY Heterocyclic Communications. ,vol. 8, pp. 593- 600 ,(2002) , 10.1515/HC.2002.8.6.593
Glenn A. Burley, Anthony G. Avent, Olga V. Boltalina, Ilya V. Gol’dt, Dirk M. Guldi, Massimo Marcaccio, Francesco Paolucci, Demis Paolucci, Roger Taylor, A light-harvesting fluorinated fullerene donor-acceptor ensemble; long-lived charge separation Chemical Communications. pp. 148- 149 ,(2003) , 10.1039/B209724A
Andrew Beeby, Martin R. Bryce, Christian A. Christensen, Graeme Cooke, Florence M. A. Duclairoir, Vincent M. Rotello, Electrochemically controlled interactions between TTF-based dendrimers and an electron-rich oligomer. Chemical Communications. pp. 2950- 2951 ,(2002) , 10.1039/B209765F
Yoshiki Morimoto, Maki Iwahashi, Takamasa Kinoshita, Koji Nishida, Stereocontrolled total synthesis of the Stemona alkaloid (-)-stenine. Chemistry: A European Journal. ,vol. 7, pp. 4107- 4116 ,(2001) , 10.1002/1521-3765(20011001)7:19<4107::AID-CHEM4107>3.0.CO;2-K
Chin-Fa Lee, Ching-Yuan Liu, Hua-Can Song, Shr-Jie Luo, Jui-Chang Tseng, Hsi-Hua Tso, Tien-Yau Luh, Bidirectional iterative synthesis of alternating benzene–furan oligomers towards molecular wires Chem. Commun.. pp. 2824- 2825 ,(2002) , 10.1039/B207881C
Christian A. Christensen, Martin R. Bryce, Andrei S. Batsanov, Jan Becher, New strategies and building blocks for functionalised 9,10-bis(1,3-dithiol-2-ylidene)-9,10-dihydroanthracene derivatives, including pyrrolo-annelated derivatives and π-extended systems with intramolecular charge-transfer Organic and Biomolecular Chemistry. ,vol. 1, pp. 511- 522 ,(2003) , 10.1039/B211153P
Mogens Brøndsted Nielsen, Zhan-Ting Li, Jan Becher, Tetrathiafulvalenophanes and theircatenanes Journal of Materials Chemistry. ,vol. 7, pp. 1175- 1187 ,(1997) , 10.1039/A700129K
Lakhemici Kaboub, Jean-Pierre Legros, Bruno Donnadieu, Abdel-Krim Gouasmia, Louiza Boudiba, Jean-Marc Fabre, Structural study and electrical conductivity of salts based on functionalized TTF containing peripheral selenium atoms Journal of Materials Chemistry. ,vol. 14, pp. 351- 356 ,(2004) , 10.1039/B308514G