ON THE VARIOUS MODES OF INTERACTION OF SULFUR WITH PHENYLATED DIYNES

References

• Senning , A. 1971 . Sulfur in Organic and Inorganic Chemistry Vol. 1 , See e.g., Marcel Dekker, New York
   Google Scholar
• Badrieh , Y. , Greenwald , A. , Schumann , H. and Blum , J. 1992 . Chem. Ber. , 125 : 667
   Google Scholar
• Sasson , Y. , Zoran , A. and Blum , J. 1981 . J. Mol. Catal. , 22 : 293
   Google Scholar
• Kvis , F. , S[vacute]atcck , E. , Zaharadnik , R. and Protiva , M. 1972 . Collect. Czech. Chem. Commun. , 37 : 3803
   Google Scholar
• Badrieh , Y. , Blum , J. , Amer , I. and Vollhardt , K. P. C. 1991 . J. Mol. Catal. , 66 : 295 See and references cited therein.
   Google Scholar
• Staab , H. A. and Draeger , B. 1972 . Chem. Ber. , 105 : 2320
   Google Scholar
• Müller , E. , Beissner , C. , Jakle , H. , Langer , E. , Muhm , H. , Odenigbo , G. , Sauerbier , M. , Segnitz , A. , Streichfuss , D. and Thomas , R. 1971 . Justus Liebigs Ann. Chem. , 754 : 64
   Google Scholar
• Bossenbroek , B. , Sanders , D. C. , Curry , H. M. and Shechter , H. 1969 . J. Am. Chem. Soc. , 91 : 371 ;
   Google Scholar
• Stabb , H. A. and Ipaktschi , J. 1971 . Chem. Ber. , 104 : 1170
   Google Scholar
• Complete crystallographic data, including tables of the FoFc values, the positional and thermal parameters, bond lengths and bond angles and stereoscopic drawing are available on request from the Cambridge Crystallographic Data Centre (CCDC) U. K., on quoting the names of the authors, and the journal citation.
   Google Scholar
• Scheller , A. , Winter , W. and Müller , E. 1976 . Justus Liebigs Ann. Chem. , : 1448
   Google Scholar
• Campbell , I. D. and Eglinton , G. 1973 . Org. Synth. Coll. , 5 : 517
   Google Scholar
• Kordts , g. B. , Richter , A. M. and Fanghaenel , E. 1991 . Monatsh. Chem. , 122 : 71 For a recent study on such compounds see e.
   Google Scholar
• Calzaferri , G. and Gleiter , R. J. 1975 . J. Chem. Soc., Perkin Trans. , 2 : 559 Theoretical studies on this system were reported by.
   Google Scholar
• Jäger , g. V. and Viehe , H. G. 1977 . Methoden der Organische Chemie Vol. 5 , 677 – 912 . For the few examples of transformation of monoalkynes and sulfur into substituted thiophenes see e., in, ed., E. Müller, Thieme Vergag, Stuttgart,/2a,pp.
   Google Scholar
• Strausz , O. P. , Font , J. , Dedio , L. F. , Kebarle , P. and Gunning , H. E. 1967 . J. Am. Chem. Soc. , 89 : 4805
   Web of Science ®Google Scholar
• Mayer , R. 1977 . Organic Chemistry of Sulfur 63 – 69 . See e.g., in, ed., S. Oae, Plenum, New York,pp.
   Google Scholar
• Abraham , T. 1953 . J. Polym. Sci. Polym. Chem. , 20 1982.
   Google Scholar
• Sheldrick , C. M. 1985 . Crystallographic Computing 175 – 189 . Oxford University Press . “3,”,pp.
   Google Scholar
• All crystallographic computing was done on a CYBER 855 computer at the Hebrew University of Jerusalem, using the TEXAN Structure Analysis Software.
   Google Scholar
• Dilthey , W. , Schommer , W. , Höschen , W. and Dierichs , H. 1959 . Ber. Dtsch. Chem. Ges. , 68 1935.
   Google Scholar