Versatile syntheses of functionalised 9,10-bis(1,3-dithiol-2-ylidene)- 9,10-dihydroanthracene derivatives

Tetrahedron Letters

Volumn 40, Issue 16, 1999, Pages 3271-3274

  Bryce, Martin R ^a   Finn, Terry ^a   Moore, Adrian J ^a  

^a DURHAM UNIVERSITY   (United Kingdom)

Author keywords

Anthracenes; Dithioles; Electron donors; Lithiation

Indexed keywords

9,10 BIS(1,3 DITHIOL 2 YLIDENE) 9,10 DIHYDROANTHRACENE; ANTHRACENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; CONFORMATION; MOLECULAR RECOGNITION; PHYSICAL CHEMISTRY; STRUCTURE ACTIVITY RELATION; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0033574467     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00381-0     Document Type: Article

References (32)

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26. Compound 2 was prepared from dibutoxyanthraquinone, by direct analogy with compound 1 (ref. 2b).
27. Garín, J.; Orduna, J.; Uriel, S.; Moore, A. J.; Bryce, M. R.; Wegener, S.; Yufit, D. S.; Howard, J. A. K. Synthesis 1994, 489.
28. Cf. Lithiation of trimethyl-TTF: Moore, A. J.; Bryce, M. R.; Batsanov, A. S.; Cole, J. C.; Howard, J. A. K. Synthesis 1995, 675.
29. 3) δ 13.1, 19.1, 25.2, 28.1, 29.6, 32.5, 36.0, 60.4, 62.8, 120.9, 123.8, 124.0, 125.3, 125.7, 126.1, 127.7, 130.2, 133.5, 134.5, 135.2 ppm.
30. Reagent 4 was obtained from the corresponding iminium salt by direct analogy with the dimethyl analogue, reported in reference 12.
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