Abstract
Both exo- and endo-isomers of 4-phenyl-3,5,8-trioxabicyclo[5.1.0]octane were reacted with thiophenol to afford individual diastereomers of hydroxy sulfides which were further processed in search for new antimycotic substances.
References
1.
Kesavan V., Bonnet-Delpon D., Bégué J.
Tetrahedron Letters,
2000
2.
Ozaki S., Matsui E., Yoshinaga H., Kitagawa S.
Tetrahedron Letters,
2000
3.
Bégué J., Bonnet-Delpon D., Kornilov A.
Synthesis,
1996
4.
Furutani T., Imashiro R., Hatsuda M., Seki M.
Journal of Organic Chemistry,
2002
5.
Sato T., Okumura Y., Itai J., Fujisawa T.
Chemistry Letters,
1988
6.
Tanikaga R., Hosoya K., Kaji A.
Journal of the Chemical Society Perkin Transactions 1,
1987
7.
Otera J., Misawa H., Sugimoto K.
Journal of Organic Chemistry,
1986
8.
Achmatowicz B., Baranowska E., Daniewski A.R., Pankowski J., Wicha J.
Tetrahedron,
1988
9.
El-Awa A., Noshi M.N., du Jourdin X.M., Fuchs P.L.
Chemical Reviews,
2009
10.
R. S. Pavelyev, E.N. Klimovitskii and L. E. Nikitina, Khimiya v Interesakh Ustoichivogo Razvitiya, 2010, 18, 775 (in Russian).
11.
BRANNOCK K.C., LAPPIN G.R.
Journal of Organic Chemistry,
1956
12.
10.1016/j.mencom.2012.05.003_bib0060
Soulier
Bull. Soc. Chim. Fr.,
1976
13.
Yamada O., Ogasawara K.
Synthesis,
1995
14.
Stepanchikova A., Lagunin A., Filimonov D., Poroikov V.
Current Medicinal Chemistry,
2003
15.
Lagunin A., Stepanchikova A., Filimonov D., Poroikov V.
Bioinformatics,
2000
16.
Poroikov V.V., Filimonov D.A., Ihlenfeldt W., Gloriozova T.A., Lagunin A.A., Borodina Y.V., Stepanchikova A.V., Nicklaus M.C.
Journal of Chemical Information and Computer Sciences,
2002