One-pot esterification and Ritter reaction: chemo-and regioselectivity from tert-butyl methyl ether
P Dawar, MB Raju, RA Ramakrishna
Index: Dawar, Pankaj; Bhagavan Raju; Ramakrishna, Ramesha A. Tetrahedron Letters, 2011 , vol. 52, # 33 p. 4262 - 4265
Full Text: HTML
Citation Number: 9
Abstract
tert-Butyl methyl ether (TBME) has been effectively used as a reagent for esterification of carboxylic acids. By varying amounts of sulfuric acid, a remarkable regioselectivity in esterification has been demonstrated. Additionally, under the present reaction conditions, one-pot esterification and Ritter reaction are achieved in almost quantitative yield.
Related Articles:
Hydrogenation of alkynes with a palladium anchored polystyrene catalyst
[Tetrahedron, , vol. 37, p. 25 - 26]
[Park, Cheon Min; Kwon, Min Serk; Park, Jaiwook Synthesis, 2006 , # 22 p. 3790 - 3794]
[Tachibana, Yuya; Masuda, Takashi; Funabashi, Masahiro; Kunioka, Masao Biomacromolecules, 2010 , vol. 11, # 10 p. 2760 - 2765]
Asymmetric hydrogenation of alkyl (vinyl) thioethers: a promising approach to α-chiral thioethers
[Tetrahedron Asymmetry, , vol. 18, # 24 p. 2849 - 2858]
[Angewandte Chemie - International Edition, , vol. 47, # 17 p. 3223 - 3226]