1959
DOI: 10.1002/ange.19590712405
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Synthese von Geranyl‐ und Farnesyl‐pyrophosphat

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Cited by 109 publications
(31 citation statements)
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“…The edges of the paper were dipped in water and the seeds were germinated at 24 C. Water was changed every day and seeds were harvested after three days. (4), as reported by Popjak et al (16). The amounts of reagents used for pyrophosphorylation, the duration of the reaction, and the final purification of the pyrophosphate esters were done according to the procedure previously described for the synthesis of farnesyl-'H pyrophosphate (18 (Table II).…”
Section: Methodsmentioning
confidence: 99%
“…The edges of the paper were dipped in water and the seeds were germinated at 24 C. Water was changed every day and seeds were harvested after three days. (4), as reported by Popjak et al (16). The amounts of reagents used for pyrophosphorylation, the duration of the reaction, and the final purification of the pyrophosphate esters were done according to the procedure previously described for the synthesis of farnesyl-'H pyrophosphate (18 (Table II).…”
Section: Methodsmentioning
confidence: 99%
“…The synthesis of both compounds was optimized in the mid80s by Davisson and Poulter during their investigations for improving the diphosphorylation step of the allylic 110 or non-allylic 111 prenyl alcohols over previously published reports [89]. Briefly, the authors found that when pyrophosphoric acid was treated with tetran-butyl ammonium hydroxide and immediately lyophilized, tris(tetra-n-butyl) ammonium hydrogen pyrophospate was obtained on a multigram scale at near quantitative yields for the displacement reaction with the corresponding activated allylic 112 and nonallylic 113 prenyl moieties.…”
Section: Syntheses Of 2c-methylerythritol 24-cyclodisphophate 95 (Cmmentioning
confidence: 99%
“…The phosphorylation o f the dolichols was carried out according to Popjak et al [20] based on the method described by Cramer and Bohm [21]. The resulting dolichol pyrophosphate was dephosphorylated to the monophosphate by hydrolysis in 1 M HCl in chloroform/methanol(2/1, v/v) for 1 h at 20 "C 1191.…”
Section: Preparation Of Exogenous Dolichol and Dolichol Phosphate Fromentioning
confidence: 99%