A New Method for Selective Activation of Amino, Hydroxy, and Mercapto Carboxylic Acids at the Carboxyl Group: Preparation of Thiol and Selenol Esters

1978 ◽  
Vol 17 (4) ◽  
pp. 267-268 ◽  
Author(s):  
Hans-Joachim Gais ◽  
Thomas Lied
ChemInform ◽  
2013 ◽  
Vol 44 (12) ◽  
pp. no-no
Author(s):  
Hikaru Yoshimura ◽  
Kohei Eto ◽  
Keisuke Takahashi ◽  
Jun Ishihara ◽  
Susumi Hatakeyama
Keyword(s):  

Synthesis ◽  
2020 ◽  
Author(s):  
Zbigniew Wróbel ◽  
Michał Tryniszewski ◽  
Robert Bujok ◽  
Roman Gańczarczyk

Tributyl- or triphenylphosphine promotes a one-pot, three-step method for the synthesis of differently substituted dibenzodiazepinones from N-aryl-2-nitroanilines. Pyridine analogues and the corresponding thiazepinones can also be formed using this method. The process involves deoxygenation of the nitro group, then formation of an iminophosphorane intermediate and its intramolecular condensation with a carboxyl group placed in the N-aryl group. The role of the carboxyl group in the formation of the iminophosphorane and the mode of cyclization are discussed.


1977 ◽  
Vol 8 (3) ◽  
pp. no-no
Author(s):  
V. N. ODINOKOV ◽  
L. P. ZHEMAIDUK ◽  
G. A. TOLSTIKOV
Keyword(s):  

1984 ◽  
Vol 61 (4) ◽  
pp. 347
Author(s):  
Ian D. Brindle ◽  
Susan Chassie

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