Complete 1H-Nmr Spectral Assignments of Six 3-Etyl Indolo[2,3-a]quinolizidine N-Oxides. NOE Difference Spectroscopy Applied to Conformational Analysis

Heterocycles ◽  
1993 ◽  
Vol 36 (10) ◽  
pp. 2373 ◽  
Author(s):  
Mauri Lounasmaa ◽  
Reija Jokela
1989 ◽  
Vol 44 (9) ◽  
pp. 1117-1123 ◽  
Author(s):  
Jasmin Jakupovic ◽  
Siegfried Huneck

The 1H NMR spectra of the following lichen substances have been correlated by NOE difference spectroscopy: atranorin, barbatic acid, diffractaic acid, nephroarctin, perlatolic acid, planaic acid methyl ester, pseudocyphellarin A, sphaerophorin (depsides), hypoprotocetraric acid, lobaric acid, pannarin, physodalic acid, psoromic acid, stictic acid (depsidones), picrolichenic acid (depsone), di-O-methyl-pannaric acid dimethylester, pannaric acid, porphyrilic acid, schizopeltic acid, strepsilin, and usnic acid (dibenzofurans).


1997 ◽  
Vol 16 (4) ◽  
pp. 507-513
Author(s):  
Anil Kumar ◽  
S. B. Katti∗ ◽  
H. Rosemeyer ◽  
Frank Seela

1996 ◽  
Vol 15 (10) ◽  
pp. 1595-1601 ◽  
Author(s):  
Anil Kumar ◽  
S. B. Katti ◽  
H. Rosemeyer ◽  
Frank Seela

1996 ◽  
Vol 43 (1) ◽  
pp. 53-64 ◽  
Author(s):  
B Golankiewicz

Tricyclic nucleosides incorporating the 9-oxo-imidazo [1,2-a]purine (1,N2-ethenoguanine) system, natural prototypes of which occur in tRNA(Phe) as nucleosides of the wyosine series, were used for synthetic, structural and biological purposes. 1,N2-(Prop-1-ene-1,2-diyl)guanosine derivatives used as intermediates allowed to enforce on guanosine the substitution at the N-3 position and at the N2 exo-amino group, not possible to be performed directly. Wyosine and 2'-deoxywyosine together with 4,5'-anhydro-4-desmethylwyosine and its congeners were used as, respectively, 100% anti and 100% syn conformation standards in a new graphical method for the syn-anti conformational analysis of nucleosides by 1D 1H NOE difference spectroscopy. Substitution at the appended third ring allowed to modify the biological and physical properties of antiviral agents acyclovir and ganciclovir, e.g. to develop their fluorescent analogues.


1992 ◽  
Vol 30 (10) ◽  
pp. 996-999 ◽  
Author(s):  
Malcolm R. Banks ◽  
Ian Gosney ◽  
Keith J. Grant ◽  
David Reed ◽  
Philip K. G. Hodgson

1985 ◽  
Vol 41 (10) ◽  
pp. 1229-1233 ◽  
Author(s):  
M.C. Reddy ◽  
B.P.Nagi Reddy ◽  
J. Ramakrishna

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