Simple Reduction of Heteroaromatic Esters to Alcohols Using a Sodium Borohydride–Methanol System

…, JS Mendonça, KC Paes, EL Fernandes…

Index: Boechat, Nubia; Da Costa, Jorge Carlos Santos; De Souza Mendonca, Jorge; Paes, Karla Ceodaro; Fernandes, Elisa Lopes; De Oliveira, Pedro Santos Mello; Vasconcelos, Thatyana Rocha Alves; De Souza, Marcus Vinicius Nora Synthetic Communications, 2005 , vol. 35, # 24 p. 3187 - 3190

Full Text: HTML

Citation Number: 8

Abstract

Abstract Some heteroaromatic esters were reduced to the corresponding alcohols by using a sodium borohydride–methanol system. The reduction was completed within 0.15–2.0 h in refluxing THF. The alcohol products were isolated after aqueous workup in moderate to excellent yield (48–97%).

Related Articles:

2-Substituted (2 SR)-2-amino-2-((1 SR, 2 SR)-2-carboxycycloprop-1-yl) glycines as potent and selective antagonists of group II metabotropic glutamate receptors. 2. …

[Ornstein, Paul L.; Bleisch, Thomas J.; Arnold, M. Brian; Wright, Rebecca A.; Johnson, Bryan G.; Schoepp, Darryle D. Journal of Medicinal Chemistry, 1998 , vol. 41, # 3 p. 346 - 357]

Novel, one-pot procedure for the synthesis of 2-arylethanol derivatives

[Schlaeger, Torsten; Oberdorf, Christoph; Tewes, Bastian; Wuensch, Bernhard Synthesis, 2008 , # 11 p. 1793 - 1797]

Investigation of the aroma-active compounds formed in the Maillard reaction between glutathione and reducing sugars

[Journal of Agricultural and Food Chemistry, , vol. 58, # 5 p. 3116 - 3124]

More Articles...