On the use of seven-membered phosphorous heterocycles based on 2,2′-dihydroxy-1,1′-binaphthalene and 1,4∶3,6-dianhydro-d-mannitol in the31P NMR analysis of the enantiomeric composition of chiral alcohols

1998 ◽  
Vol 47 (3) ◽  
pp. 411-416 ◽  
Author(s):  
A. A. Bredikhin ◽  
Z. A. Bredikhina ◽  
F. F. Nigmatzyanov
1999 ◽  
Vol 147 (1) ◽  
pp. 7-7
Author(s):  
Vladimir A. Alfonsov ◽  
Mudaris N. Dimukhametov ◽  
Guzel G. Garifzjanova ◽  
Alexander A. Bredikhin

2004 ◽  
Vol 53 (1) ◽  
pp. 213-218 ◽  
Author(s):  
A. A. Bredikhin ◽  
E. I. Strunskaya ◽  
V. G. Novikova ◽  
N. M. Azancheev ◽  
D. R. Sharafutdinova ◽  
...  

ChemInform ◽  
2004 ◽  
Vol 35 (38) ◽  
Author(s):  
A. A. Bredikhin ◽  
E. I. Strunskaya ◽  
V. G. Novikova ◽  
N. M. Azancheev ◽  
D. R. Sharafutdinova ◽  
...  

Author(s):  
Gregory H. P. Roos ◽  
Anthony R. Donovanb

The first reported acyl and sulfonylisocyanates were developed and tested in reactions with chiral alcohols to afford diastereomeric carbamates. NMR analysis of these investigates the chemical shift discrimination that would allow these activated isocyanates to be used as diagnostic probes of enantiomeric purity.


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