An expeditious preparation of all enantiopure diastereoisomers of aromatic A-ring analogues of strigolactones, germination stimulants for seeds of the parasitic weeds …
SCM Wigchert, B Zwanenburg
Index: Wigchert, Suzanne C. M.; Zwanenburg, Binne Journal of the Chemical Society - Perkin Transactions 1, 1999 , # 18 p. 2617 - 2623
Full Text: HTML
Citation Number: 14
Abstract
An expeditious manner to prepare all enantiopure diastereomers of aromatic A-ring strigolactone analogues is described. The racemic diastereoisomers of 8-methyl GR 24 and of its regioisomer 6-methyl GR 24 were prepared and separated, and subsequently chromatographed to give the pure enantiomers, using a Chiralcel OD® HPLC column. The biological activity of all enantiopure strigolactone analogues towards seeds of Striga ...
Related Articles:
[Levy, Jean-Noel; Latham, Christopher M.; Roisin, Loic; Kandziora, Nadine; Fruscia, Paolo Di; White, Andrew J. P.; Woodward, Simon; Fuchter, Matthew J. Organic and Biomolecular Chemistry, 2012 , vol. 10, # 3 p. 512 - 515]
Perhydroindanone derivatives. II. Stability relationships
[House,H.O.; Rasmusson,G.H. Journal of Organic Chemistry, 1963 , vol. 28, p. 31 - 34]
Perhydroindanone derivatives. II. Stability relationships
[House,H.O.; Rasmusson,G.H. Journal of Organic Chemistry, 1963 , vol. 28, p. 31 - 34]
[Bednarek; Zhu; Bally; Filipiak; Marcinek; Gebicki Journal of the American Chemical Society, 2001 , vol. 123, # 10 p. 2377 - 2387]
[Kobayashi, Toyoharu; Tanaka, Katsunori; Miwa, Junichi; Katsumura, Shigeo Tetrahedron Asymmetry, 2004 , vol. 15, # 2 p. 185 - 188]