“In situ”13C NMR study of ethyl alcohol interaction with sulfuric acid

1999 ◽  
Vol 68 (1) ◽  
pp. 35-43 ◽  
Author(s):  
V. B. Kazansky
2001 ◽  
Vol 11 (1) ◽  
pp. 23-25 ◽  
Author(s):  
Mikhail V. Luzgin ◽  
Alexander G. Stepanov ◽  
Vera P. Shmachkova ◽  
Nina S. Kotsarenko

2015 ◽  
Vol 51 (38) ◽  
pp. 8086-8088 ◽  
Author(s):  
L. Huang ◽  
E. G. Sorte ◽  
S.-G. Sun ◽  
Y. Y. J. Tong

The first in situ solution electrochemical 13C NMR study of ethanol oxidation on commercial Pt/C and PtRu/C was reported.


2013 ◽  
Vol 117 (10) ◽  
pp. 2102-2113 ◽  
Author(s):  
Hiroshi Kimura ◽  
Masaru Nakahara ◽  
Nobuyuki Matubayasi
Keyword(s):  
13C Nmr ◽  

1982 ◽  
Vol 257 (19) ◽  
pp. 11305-11314 ◽  
Author(s):  
J W Dillwith ◽  
J H Nelson ◽  
J G Pomonis ◽  
D R Nelson ◽  
G J Blomquist

1992 ◽  
Vol 267 (16) ◽  
pp. 11168-11175
Author(s):  
M.R. Soma ◽  
M.P. Mims ◽  
M.V. Chari ◽  
D Rees ◽  
J.D. Morrisett

Molbank ◽  
10.3390/m1236 ◽  
2021 ◽  
Vol 2021 (2) ◽  
pp. M1236
Author(s):  
Yordan Stremski ◽  
Stela Statkova-Abeghe

An convenient one-pot approach for the synthesis of new (E)-2-(2-oxo-4-phenylbut-3-en-1-yl)benzo[d]thiazole-3(2H)-carboxylates is demonstrated. The method is based on a three-component reaction of benzylideneacetone with electrophilic N-alkoxycarbonylbenzothiazolium species formed in situ. The newly synthesized compounds were fully characterized by 1D 1H, 13C- NMR, IR and MS.


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