Reductive thiolation approach to pure cyclobutyl phenyl sulfide

Organic Preparations and Procedures International

Volumn 37, Issue 2, 2005, Pages 194-197

  Fyfe, Matthew C T ^a   Rasamison, Chrystelle M ^a  

^a Prosidion Ltd   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

THIOLATION;

SULFUR COMPOUNDS;

BUTANE; CYCLOBUTYLPHENYL SULFIDE; SULFUR DERIVATIVE; THIOPHENOL; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION KINETICS; POLYMERIZATION; REACTION ANALYSIS; REDUCTION KINETICS;

EID: 19344376474     PISSN: 00304948     EISSN: 19455453     Source Type: Journal    
DOI: 10.1080/00304940509354887     Document Type: Article

References (18)

1. L. Fitjer, W. Schlotmann, and M. Noltemeyer, Tetrahedron Lett., 36, 4985 (1995).
2. G. Szeimies, A. Schlosser, F. Philipp, P. Dietz, and W. Mickler, Chem. Ber., Ill, 1922 (1978).
3. M. C. T. Fyfe, L. S. Gardner, M. Nawano, M. J. Procter, C. M. Rasamison, K. L. Schofield, V. K. Shah, and K. Yasuda, International Patent Publication WO 04/72031, 26 August 2004; Chem. Abstr., 141, 225496 (2004).
4. Y. Kikugawa, Chemistry Lett., 1157 (1981).
5. G. A. Olah, Q. Wang, N. J. Trivedi, and G. K. S. Prakash, Synthesis, 465 (1992).
6. D. J. Procter, N. J. Archer, R. A. Needham, D. Bell, A. P. Marchington, and C. M. Rayner, Tetrahedron, 55, 9611 (1999).
7. K.-h. Kim and L. S. Jimenez, Tetrahedron Asymm., 12, 999 (2001).
8. Q. Wang, X.-y. Li, G. K. S. Prakash, G. A. Olah, D. P. Loker, and K. B. Loker, ARKTVOC, 116 (2001);
9. Q. Wang, X.-y. Li, G. K. S. Prakash, G. A. Olah, D. P. Loker, and K. B. Loker, Chem. Abstr., 138, 353647 (2003).
10. J. Geiwiz, E. Goetschi, and P. Hebeisen, Synthesis, 1699 (2003).
11. G. M. Lampman and J. C. Aumiller, Org. Synth., 51, 55 (1971).
12. O. R. Gautun and P. H. J. Carlsen, Eur. J. Org. Chem., 3749 (2000).
13. G. A. Kutyrev, A. A. Kapura, R. A. Cherkasov, and A. N. Pudovik, J. Gen. Chem. USSR (Engl. Trans I.), 55, 1919 (1985);
14. G. A. Kutyrev, A. A. Kapura, R. A. Cherkasov, and A. N. Pudovik, Chem. Abstr., 105, 226744 (1986).
15. J. Salaun and A. Fadel, Org. Synth., 64, 50 (1986).
16. N. N. Greenwood and R. L. Martin, J. Chem. Soc., 1915 (1951).
17. T. Fujiwara, N. Iwasaki, and T. Takeda, Chemistry Lett., 741 (1998).
18. S. Baskaran, E. Hanan, D. Byun, and W. Shen, Tetrahedron Lett., 45, 2107 (2004).