Abstract
Treatment of nitrofurazans (NF) with sulfur nucleophiles affords a wide variety of product types, depending on the structure of both NF and S-nucleophiles.
References
1.
10.1070/MC1995v005n01ABEH000445_bib1
Khmelnitskii
Khimiya furoksanov: Reaktsii i primenenie,
1983
2.
Birckenbach L., Sennewald K.
European Journal of Organic Chemistry,
1931
3.
10.1070/MC1995v005n01ABEH000445_bib2_2
Nash
J. Chem. Soc. (C),
1969
4.
Calvino R., Fruttero R., Gasco A., Mortarini V., Aime S.
Journal of Heterocyclic Chemistry,
1982
5.
Calvino R., Serafino A., Ferrarotti B., Gasco A., Sanfilippo A.
Archiv der Pharmazie,
1984
6.
10.1070/MC1995v005n01ABEH000445_bib2_5
Rakitin
Izv. Akad. Nauk, Ser. Khim.,
1949
7.
Novikova T.S., Mel’nikova T.M., Kharitonova O.V., Kulagina V.O., Aleksandrova N.S., Sheremetev A.B., Pivina T.S., Khmel’nitskii L.I., Novikov S.S.
Mendeleev Communications,
1994
8.
Beck J.R.
Tetrahedron,
1978
9.
Sheremetev A.B., Kharitonova O.V.
Mendeleev Communications,
1992
10.
Gasco A., Mortarini V., Ruà G., Serafino A.
Journal of Heterocyclic Chemistry,
1973
11.
10.1070/MC1995v005n01ABEH000445_bib7
Solodyuk
Zh. Org. Khim.,
1981
12.
10.1070/MC1995v005n01ABEH000445_bib8
The Chemistry of Cyanates and their Thio Derivatives,
1980