N-Phthaloylglycine-derived strigol analogues. Influence of the D-ring on seed germination activity of the parasitic weeds Striga hermonthica and Orobanche crenata
JWJF Thuring, HH Bitter, MM de Kok…
Index: Thuring, Jan Willem J. F.; Bitter, Harry H.; De Kok, Margreet M.; Nefkens, Gerard H. L.; Van Riel, Annemiek M. D. A.; Zwanenburg, Binne Journal of Agricultural and Food Chemistry, 1997 , vol. 45, # 6 p. 2284 - 2290
Full Text: HTML
Citation Number: 15
Abstract
Several strigol analogues with modifications in the D-ring were synthesized and assayed for germination stimulatory activity of seeds of Striga hermonthica and Orobanche crenata. All of these D-ring analogues are derived from N-phthaloylglycine as the common ABC-fragment. It was concluded that the correct structure of the 2 (5 H)-furanone D-ring is essential to retain full biological activity. Keywords: Striga; Orobanche; germination; strigol analogue
Related Articles:
[Yoneda, Eiji; Zhang, Shi-Wei; Zhou, Da-Yang; Onitsuka, Kiyotaka; Takahashi, Shigetoshi Journal of Organic Chemistry, 2003 , vol. 68, # 22 p. 8571 - 8576]
O-silylated enolate phenylthialkylation: A synthesis of α, β-unsaturated 5-and 6-membered lactones.
[Khan, Hassan A.; Paterson, Ian Tetrahedron Letters, 1982 , vol. 23, # 48 p. 5083 - 5084]