Arylmethyl esters as protecting groups for carboxylic, carbonic and carbamic acids: deprotection via homogeneous palladium-catalyzed hydrogenolysis
A Boutros, JY Legros, JC Fiaud
Index: Tetrahedron Letters, , vol. 40, # 41 p. 7329 - 7332
Full Text: HTML
Citation Number: 12
Abstract
TETRAHEDRON LETYERS Pergamon Tetrahedron Letters 40 (1999) 7329-7332 Arylmethyl esters as protecting groups for carboxylic, carbonic ... Carbamate lb was less reactive and heating to 80°C was necessary. O 2 mol% Pd(dba)2, 2.5 mol% dppe P n_CaH170 H 4 eq. ...
Related Articles:
A ribozyme with michaelase activity: synthesis of the substrate precursors
[Eisenfuehr, Alexander; Arora, Paramjit S; Sengle, Gerhard; Takaoka, Leo R; Nowick, James S; Famulok, Michael Bioorganic and medicinal chemistry, 2003 , vol. 11, # 2 p. 235 - 249]
[Applied Catalysis A: General, , vol. 467, p. 430 - 438]
Direct oxidative cleavage of α-and β-dicarbonyls and α-hydroxyketones to diesters with KHSO5
[Journal of Organic Chemistry, , vol. 69, # 26 p. 9299 - 9302]
Direct oxidative cleavage of α-and β-dicarbonyls and α-hydroxyketones to diesters with KHSO5
[Journal of Organic Chemistry, , vol. 69, # 26 p. 9299 - 9302]
[Journal of the American Chemical Society, , vol. 108, # 7 p. 1650 - 1659]