Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Yuri E. Raifeld"'
Autor:
Irina G. Taran, Antonia A. Nikitenko, Ving J. Lee, Yuri E. Raifeld, Stanley A. Lang, Boris Arshava, Vitaly I. Shvets, Igor E. Mikerin
Publikováno v:
Tetrahedron. 54:11731-11740
The effect of A(1,3)-cis strain on the diastereoselectivity of epoxidation of (E)-and (Z)-6,6-diethoxy-3-hexen-2-ols and 4-methyl-6,6-diethoxy-3-hexen-2-ols is analyzed, with some empiric observations provided. Increased A(1,3)-cis strain results in
Autor:
Maxim V. Jasko, Antonia A. Nikitenko, Lubov S. Viktorova, Ving J. Lee, Valery E. Zavodnik, Dmitzy G. Semizarov, B. M. Arshava, Anatoly D. Shutalev, Yuri E. Raifeld, Galina V. Gurskaya, Galina Ya. Vid, Igor E. Mikerin
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:761-768
The synthesis, physicochemical properties and chain-termination properties of 3′-fluoro-3′-methyl-2′-3-dideoxythymidine is described. The synthesis was accomplished b the coupling of bis(TMS)thymine with 3-fluoro-3-methyl-2,3-dideoxy-D-erythro-
Autor:
Ving J. Lee, Yuri E. Raifeld, Igor E. Mikerin, Lubov L. Zilberg, Galina Ya. Vid, Stanley A. Lang, Antonia A. Nikitenko, B. M. Arshava
Publikováno v:
Tetrahedron. 50:8603-8616
The enantioselective synthesis of 3-substituted and 3-methyl-3-substituted 2,3-dideoxy-D- erythro -pentoses from (3 R ,4 R )-1,1-diethoxy-3,4-epoxypentane-5-ol, (3 R ,4 R) -1,1-diethoxy-3,4-epoxy-3-methylpentane-5-ol and (2 R ,3 R )-2,3-epoxy-5-hexen
Autor:
A. A. Nikitenko, Igor E. Mikerin, B. M. Arshava, Yuri E. Raifeld, S. A. Jun. Lang, Ving J. Lee
Publikováno v:
ChemInform. 24
Autor:
Igor E. Mikerin, B. M. Arshava, Ving J. Lee, Yuri E. Raifeld, G. Ya. Vid, A. A. Nikitenko, L. L. Zil'berg, S. A. Jun. Lang
Publikováno v:
ChemInform. 25
Autor:
B. M. Arshava, I. G. Taran, Ving J. Lee, Yuri E. Raifeld, V. I. Shvets, A. A. Nikitenko, Igor E. Mikerin, S. A. Jun. Lang
Publikováno v:
ChemInform. 30
Publikováno v:
Carbohydrate Research. 224:103-109
A total stereo- and enantio-selective synthesis of 2,3-dideoxy-3- C -methylene- d - glycero -pentose and its ethyl furanosides is described. The key reaction of the synthesis is formation of the 3- C -methylene function by catalytic isomerisation of
Autor:
Stanley A. Lang, Igor E. Mikerin, Yuri E. Raifeld, B. M. Arshava, A. A. Nikitenko, Ving J. Lee
Publikováno v:
Tetrahedron Letters. 33:7087-7088
The cleavage of the oxirane ring of 3,4-anhydro-2deoxy-D-threo-pentose diethyl acetal by (isopropoxy)-titanium fluorides is discussed. The high regioselectivity found with bis(isopropoxy)titanium difluoride is the basis for an enantioselective synthe
Publikováno v:
Tetrahedron: Asymmetry. 2:1083-1084
Substituted titanium (IV) triisopropoxides [( i -PrO) 3 TiX] are highly effective reagents for the regioselective ring opening of 2,3-epoxyalcohols.