Oxidative Amide Synthesis and N-Terminal α-Amino Group Ligation of Peptides in Aqueous Medium

2006 ◽  
Vol 128 (46) ◽  
pp. 14796-14797 ◽  
Author(s):  
Wing-Kei Chan ◽  
Chi-Ming Ho ◽  
Man-Kin Wong ◽  
Chi-Ming Che
ChemInform ◽  
2007 ◽  
Vol 38 (12) ◽  
Author(s):  
Wing-Kei Chan ◽  
Chi-Ming Ho ◽  
Man-Kin Wong ◽  
Chi-Ming Che

2013 ◽  
Vol 781-784 ◽  
pp. 287-290 ◽  
Author(s):  
Rui Liu ◽  
Hong Li ◽  
Wen Yan Ma

Methodology has been sought towards 1,4-naphthoquinone bearing amino group and hydroxyl group in the quinonoid ring. In the first of these objectives, 2-Hydroxy-3-nitro-1,4-naphthoquinone was synthesized by two kinds of improved method giving moderate yield. Then treatment of 2-hydroxy-3-nitro-1,4-naphthoquinone with stannous chloride in aqueous medium afforded 2-hydroxy-3-amino-1,4-naphthoquinone. The chemical structure of the product obtained by the process of the present study was verified by IR and NMR.


ChemInform ◽  
2012 ◽  
Vol 43 (33) ◽  
pp. no-no
Author(s):  
Gai-Li Li ◽  
Karen Ka-Yan Kung ◽  
Man-Kin Wong

2012 ◽  
Vol 48 (34) ◽  
pp. 4112 ◽  
Author(s):  
Gai-Li Li ◽  
Karen Ka-Yan Kung ◽  
Man-Kin Wong

2005 ◽  
Vol 123 ◽  
pp. 341-344
Author(s):  
A. Khaldoun ◽  
F. González-Caballero ◽  
J. G. López-Durán ◽  
N. Mahrach ◽  
M. L. Kerkeb

1965 ◽  
Vol 15 (10) ◽  
pp. 479-488
Author(s):  
R. C. Clark ◽  
W. G. Cobbett ◽  
J. A. Gibbs ◽  
R. T. Jones ◽  
A. A. Leach ◽  
...  
Keyword(s):  

2017 ◽  
Vol 39 (1) ◽  
pp. 46-52
Author(s):  
T. SAVCHENKO ◽  
◽  
A. GRECHANOVSKY ◽  
A. BRIK ◽  
N. DUDCHENKO

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