Chemoselective Hydrolysis of tert-Butyl Esters in Acetonitrile Using Molecular Iodine as a Mild and Efficient Catalyst.

ChemInform ◽  
2006 ◽  
Vol 37 (42) ◽  
Author(s):  
J. S. Yadav ◽  
E. Balanarsaiah ◽  
S. Raghavendra ◽  
M. Satyanarayana
Keyword(s):  
Molecular Iodine ◽  
Efficient Catalyst ◽  
Tert Butyl ◽  
Butyl Esters ◽  
Hydrolysis Of

Chemoselective hydrolysis of tert-butyl esters in acetonitrile using molecular iodine as a mild and efficient catalyst

2006 ◽  
Vol 47 (28) ◽  
pp. 4921-4924 ◽  
Author(s):  
J.S. Yadav ◽  
E. Balanarsaiah ◽  
S. Raghavendra ◽  
M. Satyanarayana
Keyword(s):  
Molecular Iodine ◽  
Efficient Catalyst ◽  
Tert Butyl ◽  
Butyl Esters ◽  
Hydrolysis Of

ChemInform Abstract: Titanium Tetrachloride Promoted Hydrolysis of Cephalosporin tert-Butyl Esters.

ChemInform ◽  
2010 ◽  
Vol 29 (22) ◽  
pp. no-no
Author(s):  
M. VALENCIC ◽  
T. VAN DER DOES ◽  
E. DE VROOM
Keyword(s):  
Titanium Tetrachloride ◽  
Tert Butyl ◽  
Butyl Esters ◽  
Hydrolysis Of

Titanium tetrachloride promoted hydrolysis of cephalosporin tert-butyl esters

1998 ◽  
Vol 39 (12) ◽  
pp. 1625-1628 ◽  
Author(s):  
Marjan Valencic ◽  
Thom van der Does ◽  
Erik de Vroom
Keyword(s):  
Titanium Tetrachloride ◽  
Tert Butyl ◽  
Butyl Esters ◽  
Hydrolysis Of

Chemoselective hydrolysis of terminal isopropylidene acetals in acetonitrile using molecular iodine as a mild and efficient catalyst

2005 ◽  
Vol 46 (50) ◽  
pp. 8745-8748 ◽  
Author(s):  
J.S. Yadav ◽  
M. Satyanarayana ◽  
S. Raghavendra ◽  
E. Balanarsaiah
Keyword(s):  
Molecular Iodine ◽  
Efficient Catalyst ◽  
Hydrolysis Of

Chemoselective Hydrolysis of Terminal Isopropylidene Acetals in Acetonitrile Using Molecular Iodine as a Mild and Efficient Catalyst.

ChemInform ◽  
2006 ◽  
Vol 37 (13) ◽  
Author(s):  
J. S. Yadav ◽  
M. Satyanarayana ◽  
S. Raghavendra ◽  
E. Balanarsaiah
Keyword(s):  
Molecular Iodine ◽  
Efficient Catalyst ◽  
Hydrolysis Of

Selective enzymatic hydrolysis of C-terminal tert-butyl esters of peptides

2009 ◽  
pp. 115-116
Author(s):  
Carmen G. Boeriu ◽  
Ivo F. Eggen ◽  
Dirk-Jan van Zoelen ◽  
Gilbert H. Bours
Keyword(s):  
Enzymatic Hydrolysis ◽  
Tert Butyl ◽  
Butyl Esters ◽  
Hydrolysis Of

Fe(ClO4)3·H2O-Catalyzed Ritter Reaction: A Convenient Synthesis of Amides from Esters and Nitriles

Synlett ◽  
2018 ◽  
Vol 29 (17) ◽  
pp. 2257-2264 ◽  
Author(s):  
Min Ji ◽  
Chengliang Feng ◽  
Bin Yan ◽  
Guibo Yin ◽  
Junqing Chen
Keyword(s):  
Solvent Free ◽  
Ritter Reaction ◽  
Efficient Catalyst ◽  
Tert Butyl ◽  
Butyl Esters ◽  
Convenient Synthesis ◽  
Solvent Free Conditions ◽  
Aryl Nitriles ◽  
The Ritter Reaction

An efficient and inexpensive synthesis of N-substituted amides from the Ritter reaction of nitriles with esters catalyzed by Fe(ClO4)3·H2O is described. Fe(ClO4)3·H2O is an economically efficient catalyst for the Ritter reaction under solvent-free conditions. Reactions of a range of esters (benzyl, sec-alkyl, and tert-butyl esters) with nitriles (primary, secondary, tertiary, and aryl nitriles) were performed to provide the corresponding amides in high to excellent yields.

Sign in / Sign up

Export Citation Format

Share Document