An efficient procedure for the preparation of Fmoc-amino acids

SP Raillard, AD Mann, TA Baer

Index: Organic Preparations and Procedures International, , vol. 30, # 2 p. 183 - 186

Full Text: HTML

Citation Number: 13

Abstract

... 1998 by Organic Preparations and Procedures Inc. ... The organic phase was washed with water and brine and then dried over sodium sulfate ... Preparation of 4-(4-[1-(9-Fluorenylmethoxycarb onylamino)ethyl]-2-methoxy-5-nitrophenoxy}- butanoic Acid (2).- To a slurry of amino acid ...

Related Articles:

Enantioselective total synthesis of eudistomidins G, H, and I

[Ishiyama, Haruaki; Yoshizawa, Kazuaki; Kobayashi, Jun'ichi Tetrahedron, 2012 , vol. 68, # 31 p. 6186 - 6192]

Alternative and Chemoselective Deprotection of the α??Amino and Carboxy Functions of N??Fmoc??Amino Acid and N??Fmoc??Dipeptide Methyl Esters by Modulation of …

[Di Gioia, Maria Luisa; Leggio, Antonella; Le Pera, Adolfo; Liguori, Angelo; Perri, Francesca; Siciliano, Carlo European Journal of Organic Chemistry, 2004 , # 21 p. 4437 - 4441]

Alkyl 1-chloroalkyl carbonates: Reagents for the synthesis of carbamates and protection of amino groups

[Barcelo, Gerard; Senet, Jean-Pierre; Sennyey, Gerard; Bensoam, Jean; Loffet, Albert Synthesis, 1986 , # 8 p. 627 - 632]

A mild and selective method for the cleavage of tert-butyl esters

[Jackson, Randy W Tetrahedron Letters, 2001 , vol. 42, # 31 p. 5163 - 5165]

5-Norbornene-2, 3-dicarboximido carbonochloridate. A new stable reagent for the introduction of amino-protecting groups

[Henklein, Peter; Heyne, Hans-Ulrich; Halatsch, Wolf-Rainer; Niedrich, Hartmut Synthesis, 1987 , # 2 p. 166 - 167]

More Articles...