Triazolyl derivatives for acidic release of alcohols

M Mondon, R Delatouche, C Bachmann…

Index: Mondon, Martine; Delatouche, Regis; Bachmann, Christian; Frapper, Gilles; Len, Christophe; Bertrand, Philippe European Journal of Organic Chemistry, 2011 , # 11 p. 2111 - 2119

Full Text: HTML

Citation Number: 5

Abstract

Abstract New triazolyl-based carbonates and ethers have been investigated as potential alcohol-releasing systems under mild acidic conditions. Triazolyl carbonates could not be prepared because of their apparent instability, whereas ethers were successfully obtained. The rate of hydrolysis of these ethers ramged from a few hours to several days. A theoretical investigation demonstrated that the acidic release of alcohols from triazole derivatives ...

~90%

The Intricate Assembling of gem??Diphenylpropargylic Units

[Maraval, Valerie; Duhayon, Carine; Coppel, Yannick; Chauvin, Remi European Journal of Organic Chemistry, 2008 , # 30 p. 5144 - 5156]

Synthesis of α-Substituted Enoximes with Nucleophiles via Ni...

[Zhang, Huan; Tanimoto, Hiroki; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Kakiuchi, Kiyomi Organic Letters, 2013 , vol. 15, # 20 p. 5222 - 5225]

Photochromic Behaviour of Bis [4-(N, N-dimethylamino) phenyl...

[Harie, Guenaelle; Samat, Andre; Guglielmetti, Robert; De Keukeleire, Denis; Saeyens, Wim; Van Parys, Inge Tetrahedron Letters, 1997 , vol. 38, # 17 p. 3075 - 3078]

Design of pH responsive clickable prodrugs applied to histon...

[Delatouche, Regis; Denis, Iza; Grinda, Marion; Bahhaj, Fatima El; Baucher, Estelle; Collette, Floraine; Heroguez, Valerie; Gregoire, Marc; Blanquart, Christophe; Bertrand, Philippe European Journal of Pharmaceutics and Biopharmaceutics, 2013 , vol. 85, # 3 PART B p. 862 - 872]