Zobrazeno 1 - 4
of 4
pro vyhledávání: '"G. V. Chel'tsova-Bebutova"'
Publikováno v:
Russian Chemical Bulletin. 44:873-877
The determination of the enantiomeric composition of chiral compounds by1H,13C, and31P NMR spectroscopy in the presence of (S)-1,1′-binaphthyl-2,2′-diol demonstrates that the enantioselectivity of the method increases when the polarity of a solve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc1ce11678345ce2174293324aff68a1
https://doi.org/10.1007/bf00696919
https://doi.org/10.1007/bf00696919
Autor:
L. N. Kalgorodova, G. I. Nikishin, Maxim G. Vinogradov, A. V. Ignatenko, E. K. Starostin, G. V. Chel'tsova-Bebutova, L. S. Gorshkova, E. A. Shapiro
Publikováno v:
Russian Chemical Bulletin. 44:167-171
A convenient preparative synthesis of cilastatin, an inhibitor of renal dipeptidase used in drugs with the antibiotic imipenem, has been elaborated. The key intermediate in this synthesis is 2-amino-7-chloroheptanoic acid prepared by oxidative cleava
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::757003c8c9d2970bc739c682a13a3db1
https://doi.org/10.1007/bf00696982
https://doi.org/10.1007/bf00696982
Autor:
E. K. Starostin, Maxim G. Vinogradov, L. N. Kaigorodova, L. S. Gorshkova, A. V. Ignatenko, G. I. Nikishin, E. A. Shapiro, G. V. Chel'tsova-Bebutova
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39e9e22840f5a1ba04ed4cf151a02c84
https://doi.org/10.1002/chin.199530234
https://doi.org/10.1002/chin.199530234
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 36:1472-1475
The stereoselectivity of hydrogenation of methyl esters of N-trifluoroacetyl dehydrodipeptides on a Ni-catalyst was determined by the structure of the C-terminal residue and the prochiral center. The S-configuration of the C-terminal amino acid leads
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0fc65f0ad9ea05a5af2b3d20de4c9e8
https://doi.org/10.1007/bf01557526
https://doi.org/10.1007/bf01557526