1H and13C NMR data of benzylsulfonic acids—model compounds for lignosulfonate

2008 ◽  
Vol 46 (3) ◽  
pp. 299-305 ◽  
Author(s):  
Bjart F. Lutnaes ◽  
Bernt O. Myrvold ◽  
Rolf A. Lauten ◽  
Molla M. Endeshaw
Planta Medica ◽  
1987 ◽  
Vol 53 (01) ◽  
pp. 77-80 ◽  
Author(s):  
Frederik Fischer ◽  
Marion Gijbels
Keyword(s):  

2015 ◽  
Vol 54 (4) ◽  
pp. 268-290 ◽  
Author(s):  
Víctor Gómez-Calvario ◽  
María Luisa Garduño-Ramírez ◽  
Ismael León-Rivera ◽  
María Yolanda Rios

2007 ◽  
Vol 45 (8) ◽  
pp. 674-679 ◽  
Author(s):  
Younghee Park ◽  
Byoung-Ho Moon ◽  
Eunjung Lee ◽  
Youngshim Lee ◽  
Youngdae Yoon ◽  
...  
Keyword(s):  

2006 ◽  
Vol 44 (10) ◽  
pp. 980-983 ◽  
Author(s):  
Kirsten J. Goodall ◽  
Margaret A. Brimble ◽  
David Barker
Keyword(s):  

1978 ◽  
Vol 56 (24) ◽  
pp. 3117-3120 ◽  
Author(s):  
Suzanne Lesage ◽  
Arthur S. Perlin

13C nmr data indicate that the epoxypropyl side chain of 'asperlin' (1) has a trans configuration. This assignment follows from associated measurements on model compounds, showing that the 13C chemical shift of an epoxypropyl CH3 group is close to either 17 ppm (trans isomers) or 13 ppm (cis isomers). Synthesized as oxirane derivatives related to 1 are diastereomeric pairs of 8-deoxy-6,7-cis- and -trans-epoxy-1,2:3,4-di-O-isopropylidene-α-D-galacto-octopyranoses.


1991 ◽  
Vol 29 (6) ◽  
pp. 641-643 ◽  
Author(s):  
André De Bruyn ◽  
Georges Verhegge ◽  
Fernand Lambein

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