Fmoc*: A More Soluble Analogue of the 9-Fluorenylmethoxycarbonyl Protecting Group
KD Stigers, MR Koutroulis, DM Chung…
Index: Stigers, Kimberly D.; Koutroulis, Mathew R.; Chung, De Michael; Nowick, James S. Journal of Organic Chemistry, 2000 , vol. 65, # 12 p. 3858 - 3859
Full Text: HTML
Citation Number: 42
Abstract
Materials and Methods. Commercial-grade reagents and solvents were used without further purification except as indicated. CH2Cl2 and THF were dried prior to use by percolation through anhydrous Al2O3 as described by Grubbs and coworkers. 10 Fluorene was recrystallized from ethanol. n-Butyllithium was titrated with 2-butanol using 1, 10- phenanthroline as indicator and toluene as solvent. 11 p-Methoxybenzylamine was ...
Related Articles:
2, 7-Di-tert-butyl-Fmoc-P-OSu: A new polymer-Supported reagent for the protection of the amino group
[Chinchilla, Rafael; Dodsworth, David J; Najera, Carmen; Soriano, Jose M Bioorganic and medicinal chemistry letters, 2002 , vol. 12, # 14 p. 1817 - 1820]