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pro vyhledávání: '"Goldsmith Miriam E"'
Publikováno v:
Pest Management Science. 73:743-751
BACKGROUND We hypothesized that the exploration of chemical space around compounds with reported insecticidal activity could be a viable strategy for discovering novel, insecticidally active areas of chemistry. RESULTS A series of thioureas and isoth
Akademický článek
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Publikováno v:
Synthetic Communications. 26:1423-1429
A convenient method for the synthesis of mono N-substituted guanylthioureas in reasonable yields from readily available starting materials has been developed. In contrast to the previously published method, the use of highly noxious hydrogen sulfide
Publikováno v:
Tetrahedron Letters. 35:3025-3028
Beckmann rearrangement of erythromycin A 9(E)-oxime with toluenesulfonyl chloride in ethyl ether at −45°C generates 9,11-imino ether IV which leads to azithromycin. The 9,11-imino ether can also be readily obtained from isomerization of its isomer
Publikováno v:
ChemInform. 27
A convenient method for the synthesis of mono N-substituted guanylthioureas in reasonable yields from readily available starting materials has been developed. In contrast to the previously published method, the use of highly noxious hydrogen sulfide
Publikováno v:
Synthetic Communications; Apr1996, Vol. 26 Issue 7, p1423-1429, 7p
Autor:
Lyman R. Caswell, Goldsmith Miriam E
Publikováno v:
The Journal of Organic Chemistry. 54:5101-5104