Zobrazeno 1 - 9
of 9
pro vyhledávání: '"G. R. Sunagatullina"'
Publikováno v:
Russian Journal of Organic Chemistry. 58:724-726
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69348e9b6bfaa6c9d6f61640445f3d7b
https://doi.org/10.1134/s107042802205013x
https://doi.org/10.1134/s107042802205013x
Publikováno v:
Russian Journal of Organic Chemistry. 57:889-904
A new chiral 10,11-didehydro analog of epothilone D with isosteric substitution in the C15–C3 fragment of natural epothilones has been synthesized.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfe352f286200121163a33a25fb4c471
https://doi.org/10.1134/s1070428021060038
https://doi.org/10.1134/s1070428021060038
Publikováno v:
Russian Journal of Organic Chemistry. 56:1140-1145
Yamaguchi esterification of (2Z,5S,6E)-5-(hydroxymethyl)-2,6-dimethyl-7-(2-methyl-1,3-thiazol-4-yl)hepta-2,6-dienal with (2R,5R,6S,7S)-2-(methoxymethoxy)-3,3,5,7-tetramethyl-4-oxo-9-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl-6-[(triethylsilyl)oxy]nonanoic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5a6135fd0687396f8a11bea972e2cb8
https://doi.org/10.1134/s1070428020070039
https://doi.org/10.1134/s1070428020070039
Publikováno v:
Russian Journal of Organic Chemistry. 55:1370-1373
A synthetic approach is described for the transformation of R-(-)-carvone to methyl (2Z,5S,6E)-5-[(tert-butoxycarbonyl)amino]-2,6-dimethyl-7-(2-methyl-1,3-thiazol-4-yl)hepta-2,6-dienoate, the key building block for the convergent synthesis of the kno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::042dc19648a242a4c60cbd26b613a36a
https://doi.org/10.1134/s1070428019090161
https://doi.org/10.1134/s1070428019090161
Publikováno v:
Mendeleev Communications. 31:696-697
R-Carvone on heating with Pb(OAc)4 in benzene gives (2RS)-2-hydroxy-2-[(1S)-4-methyl-5-oxocyclohex-3-en-1-yl)]-prop-1-yl bis(acetoxy)acetate. Alkaline hydrolysis of this compound affords the corresponding diol which under acidic catalysis is transfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::749a0e78ccb84968fb1853fb2e36c6c6
https://doi.org/10.1016/j.mencom.2021.09.034
https://doi.org/10.1016/j.mencom.2021.09.034
Publikováno v:
Russian Journal of Organic Chemistry. 54:1548-1552
The synthesis of acyclic precursors to epothilone D analogs has been explored. Optimal conditions have been found for enolization of (1R)-1-(1,3-dithiolan-2-yl)-1-(methoxymethoxy)-2,2-dimethylpentan-3-one and its aldol condensation with C6‒C21 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::684cd489d6b8c07c6a76efed25cbf788
https://doi.org/10.1134/s1070428018100172
https://doi.org/10.1134/s1070428018100172
Publikováno v:
Russian Journal of Organic Chemistry. 55:1439-1441
Coupling of previously synthesized chiral building blocks via Yamaguchi esterification has been studied with the goal of obtaining epothilone D isosteres. Some peculiar features of the Yamaguchi esterification stage have been revealed, which are rela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1375eeeaa9972edf74489f7593f861e
https://doi.org/10.1134/s1070428019090264
https://doi.org/10.1134/s1070428019090264
Publikováno v:
Russian Journal of Organic Chemistry. 53:1687-1690
Synthesis was developed of a new chiral block for epothilone analogs from R-(‒)-pantolactone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ddb40ad2d5fcc6d29b6fa717fca2592
https://doi.org/10.1134/s1070428017110136
https://doi.org/10.1134/s1070428017110136
Publikováno v:
Mendeleev Communications. 28:587-588
Condensation of separately obtained C1–C9 and C10–C21 chiral blocks under Yamaguchi conditions affords the corresponding ester, an acyclic precursor of an epothilone D analogue. The reaction is accompanied by the formation of a side product of ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d3ed332aaf537c4889b43368e138d78
https://doi.org/10.1016/j.mencom.2018.11.007
https://doi.org/10.1016/j.mencom.2018.11.007