-
1
-
-
34250900985
-
Recent advances in the synthesis of unnatural α-amino acids
-
Perdih A, Dolenc MS. Recent advances in the synthesis of unnatural α-amino acids. Curr. Org. Chem. 11, 801-832 (2007).
-
(2007)
Curr. Org. Chem.
, vol.11
, pp. 801-832
-
-
Perdih, A.1
Dolenc, M.S.2
-
2
-
-
0003416163
-
-
Kukhar VP, Soloshonok VA (Eds). John Wiley & Sons, Chichester, UK
-
Kukhar VP, Soloshonok VA (Eds). Fluorine-Containing Amino Acids. John Wiley & Sons, Chichester, UK (1995).
-
(1995)
Fluorine-Containing Amino Acids
-
-
-
5
-
-
27844536987
-
Asymmetric synthesis of fluorine and phosphorus-containing amino acids
-
Kukhar VP, Svistunova NY, Solodenko VA, Soloshonok VA. Asymmetric synthesis of fluorine and phosphorus-containing amino acids. Russ. Chem. Rev. 62, 261-278 (1993).
-
(1993)
Russ. Chem. Rev.
, vol.62
, pp. 261-278
-
-
Kukhar, V.P.1
Svistunova, N.Y.2
Solodenko, V.A.3
Soloshonok, V.A.4
-
7
-
-
3142782003
-
Synthesis of fluorinated amino acids
-
Qiu XL, Meng WD, Qing FL. Synthesis of fluorinated amino acids. Tetrahedron 60, 6711-6745 (2004).
-
(2004)
Tetrahedron
, vol.60
, pp. 6711-6745
-
-
Qiu, X.L.1
Meng, W.D.2
Qing, F.L.3
-
8
-
-
0034353232
-
Synthesis of fluorinated amino acids
-
Sutherland A, Willis CL. Synthesis of fluorinated amino acids. Nat. Prod. Rep. 17, 621-631 (2000).
-
(2000)
Nat. Prod. Rep.
, vol.17
, pp. 621-631
-
-
Sutherland, A.1
Willis, C.L.2
-
9
-
-
0036430153
-
Fluorinated amino acids in protein design and engineering
-
Yoder NC, Kumar K. Fluorinated amino acids in protein design and engineering. Chem. Soc. Rev. 31, 335-341 (2002).
-
(2002)
Chem. Soc. Rev.
, vol.31
, pp. 335-341
-
-
Yoder, N.C.1
Kumar, K.2
-
11
-
-
49449097238
-
The many roles for fluorine in medicinal chemistry
-
Hagmann WK. The many roles for fluorine in medicinal chemistry. J. Med. Chem. 51, 4359-4369 (2008).
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4359-4369
-
-
Hagmann, W.K.1
-
12
-
-
33751408183
-
Bioorthogonal noncovalent chemistry: Fluorous phases in chemical biology
-
Yoder NC, Yüksel D, Dafik L, Kumar K. Bioorthogonal noncovalent chemistry: fluorous phases in chemical biology. Curr. Opin. Chem. Biol. 10, 576-583 (2006).
-
(2006)
Curr. Opin. Chem. Biol.
, vol.10
, pp. 576-583
-
-
Yoder, N.C.1
Yüksel, D.2
Dafik, L.3
Kumar, K.4
-
13
-
-
33645454126
-
Fluorine in medicinal chemistry: A review of anti-cancer agents
-
Isanbor C, O'Hagan D. Fluorine in medicinal chemistry: a review of anti-cancer agents. J. Fluor. Chem. 127, 303-319 (2006).
-
(2006)
J. Fluor. Chem.
, vol.127
, pp. 303-319
-
-
Isanbor, C.1
O'Hagan, D.2
-
14
-
-
33746356860
-
Recent advances (1995-2005) in fluorinated pharmaceuticals based on natural products
-
Bégué JP, Bonnet-Delpon D. Recent advances (1995-2005) in fluorinated pharmaceuticals based on natural products. J. Fluor. Chem. 127, 992-1012 (2006).
-
(2006)
J. Fluor. Chem.
, vol.127
, pp. 992-1012
-
-
Bégué, J.P.1
Bonnet-Delpon, D.2
-
15
-
-
33746372978
-
Fluorine in medicinal chemistry: Recent therapeutic applications of fluorinated small molecules
-
Kirk KL. Fluorine in medicinal chemistry: recent therapeutic applications of fluorinated small molecules. J. Fluorine Chem. 127, 1013-1029 (2006).
-
(2006)
J. Fluorine Chem.
, vol.127
, pp. 1013-1029
-
-
Kirk, K.L.1
-
16
-
-
4544288081
-
Probing the proteolytic stability of Β-peptides containing α-fluoro- and α-hydroxy-Β-amino acids
-
Hook DF, Gessier F, Noti C, Kast P, Seebach D. Probing the proteolytic stability of Β-peptides containing α-fluoro- and α-hydroxy- Β-amino acids. Chem. Bio. Chem. 5, 691-706 (2004).
-
(2004)
Chem. Bio. Chem.
, vol.5
, pp. 691-706
-
-
Hook, D.F.1
Gessier, F.2
Noti, C.3
Kast, P.4
Seebach, D.5
-
17
-
-
52149106900
-
Noncovalent associations in fluorous fluids
-
Vincent JM. Noncovalent associations in fluorous fluids. J. Fluor. Chem. 129, 903-909 (2008).
-
(2008)
J. Fluor. Chem.
, vol.129
, pp. 903-909
-
-
Vincent, J.M.1
-
18
-
-
4544318450
-
Fluorine interactions at the thrombin active site: Protein backbone fragments H-C-C=O comprise a favorable C-F environment and interactions of C-F with electrophiles
-
Olsen JA, Banner DW, Seiler P et al. Fluorine interactions at the thrombin active site: protein backbone fragments H-C-C=O comprise a favorable C-F environment and interactions of C-F with electrophiles. Chem. Bio. Chem. 5, 666-675 (2004).
-
(2004)
Chem. Bio. Chem.
, vol.5
, pp. 666-675
-
-
Olsen, J.A.1
Banner, D.W.2
Seiler, P.3
-
19
-
-
0037663879
-
A fluorine scan of thrombin inhibitors to map the fluorophilicity/ fluorophobicity of an enzyme active site: Evidence for C-F•••C=O interactions
-
Olsen JA, Banner DW, Seiler P et al. A fluorine scan of thrombin inhibitors to map the fluorophilicity/fluorophobicity of an enzyme active site: evidence for C-F•••C=O interactions. Angew. Chem. Int. Ed. Engl. 42, 2507-2511 (2003).
-
(2003)
Angew. Chem. Int. Ed. Engl.
, vol.42
, pp. 2507-2511
-
-
Olsen, J.A.1
Banner, D.W.2
Seiler, P.3
-
20
-
-
4944240542
-
A weak attractive interaction between organic fluorine and an amide group
-
Hof F, Scofield DM, Schweizer WB, Diederich F. A weak attractive interaction between organic fluorine and an amide group. Angew. Chem. Int. Ed. Engl. 43, 5056-5059 (2004).
-
(2004)
Angew. Chem. Int. Ed. Engl.
, vol.43
, pp. 5056-5059
-
-
Hof, F.1
Scofield, D.M.2
Schweizer, W.B.3
Diederich, F.4
-
21
-
-
42949127288
-
The trifluoroethylamine function as peptide bond replacement
-
Sani M, Volonterio A, Zanda M. The trifluoroethylamine function as peptide bond replacement. ChemMedChem 2, 1693-1700 (2007).
-
(2007)
Chem Med Chem
, vol.2
, pp. 1693-1700
-
-
Sani, M.1
Volonterio, A.2
Zanda, M.3
-
22
-
-
54849405131
-
Intracellular uptake and inhibitory activity of aromatic fluorinated amino acids in human breast cancer cells
-
Giese C, Lepthien S, Metzner L, Brandsch M, Budisa N, Lilie H. Intracellular uptake and inhibitory activity of aromatic fluorinated amino acids in human breast cancer cells. ChemMedChem 3, 1449-1456 (2008).
-
(2008)
ChemMedChem
, vol.3
, pp. 1449-1456
-
-
Giese, C.1
Lepthien, S.2
Metzner, L.3
Brandsch, M.4
Budisa, N.5
Lilie, H.6
-
23
-
-
4544274902
-
Alternative translations of a single rna message: An identity switch of (2S,3R)-44,4- trifluorovaline between valine and isoleucine codons
-
Wang P, Fichera A, Kumar K, Tirrell DA. Alternative translations of a single rna message: an identity switch of (2S,3R)-4,4,4- trifluorovaline between valine and isoleucine codons. Angew. Chem. Int. Ed. Engl. 43, 3664-3666 (2004).
-
(2004)
Angew. Chem. Int. Ed. Engl.
, vol.43
, pp. 3664-3666
-
-
Wang, P.1
Fichera, A.2
Kumar, K.3
Tirrell, D.A.4
-
24
-
-
0342578108
-
Fluorine-containing amino acids. I. an efficient synthesis of D,L-α, α, α-trifluoroalanine
-
Yagupolskii YL, Soloshonok VA, Kukhar VP. Fluorine-containing amino acids. i. an efficient synthesis of D,L-α, α, α- trifluoroalanine. Zh. Org. Khim. 22, 517-521 (1986).
-
(1986)
Zh. Org. Khim.
, vol.22
, pp. 517-521
-
-
Yagupolskii, Y.L.1
Soloshonok, V.A.2
Kukhar, V.P.3
-
25
-
-
0001406543
-
Fluorine-containing amino acids. V. Imines of trifluoropyruvic acid in the synthesis of n-substituted trifluoroalanines
-
Soloshonok VA, Yagupolskii YL, Kukhar VP. Fluorine-containing amino acids. V. Imines of trifluoropyruvic acid in the synthesis of n-substituted trifluoroalanines. Zh. Org. Khim. 24, 1638-1644 (1988).
-
(1988)
Zh. Org. Khim.
, vol.24
, pp. 1638-1644
-
-
Soloshonok, V.A.1
Yagupolskii, Y.L.2
Kukhar, V.P.3
-
27
-
-
0000171574
-
Fluorine-containing amino acids. Iii. A-trifluoromethyl-α-amino acids
-
Soloshonok VA, Gerus II, Yagupolskii YL, Kukhar VP. Fluorine-containing amino acids. Iii. A-trifluoromethyl-α-amino acids. Zh. Org. Khim. 23, 2308-2313 (1987).
-
(1987)
Zh. Org. Khim.
, vol.23
, pp. 2308-2313
-
-
Soloshonok, V.A.1
Gerus, I.I.2
Yagupolskii, Y.L.3
Kukhar, V.P.4
-
28
-
-
0026520631
-
Novel approach to the synthesis of symmetric optically active 2,5-dioxopiperazines
-
Basiuk VA, Gromovoy TY, Chuiko AA, Soloshonok VA, Kukhar VPA. Novel approach to the synthesis of symmetric optically active 2,5-dioxopiperazines. Synthesis 449-451 (1992).
-
(1992)
Synthesis
, pp. 449-451
-
-
Basiuk, V.A.1
Gromovoy, T.Y.2
Chuiko, A.A.3
Soloshonok, V.A.4
Kukhar, V.P.A.5
-
29
-
-
0006208463
-
Reactions of methyl trifluoropyruvate and its N-(methoxycarbonyl)imine with φ-rich heterocycles and dipolar compounds
-
Soloshonok VA, Kukhar VP. Reactions of methyl trifluoropyruvate and its N-(methoxycarbonyl)imine with φ-rich heterocycles and dipolar compounds. Zh. Org. Khim. 26, 419-425 (1990)
-
(1990)
Zh. Org. Khim.
, vol.26
, pp. 419-425
-
-
Soloshonok, V.A.1
Kukhar, V.P.2
-
30
-
-
34249975735
-
Aminoalkylation of α-picoline by methyl 2-trifluoroacetylimino-3,3, 3- trifluoropropionate
-
Osipov SN, Chkanikov ND, Kolomiets AF, Fokin AV. Aminoalkylation of α-picoline by methyl 2-trifluoroacetylimino-3,3,3- trifluoropropionate. Russian Chem. Bull. 38, 201 (1989).
-
(1989)
Russian Chem. Bull.
, vol.38
, pp. 201
-
-
Osipov, S.N.1
Chkanikov, N.D.2
Kolomiets, A.F.3
Fokin, A.V.4
-
32
-
-
43549085582
-
Triflic acid-catalyzed highly stereoselective friedel-crafts aminoalkylation of indoles and pyrroles
-
Abid M, Teixeira L, Török B. Triflic acid-catalyzed highly stereoselective friedel-crafts aminoalkylation of indoles and pyrroles. Org. Lett. 10, 933-935 (2008).
-
(2008)
Org. Lett.
, vol.10
, pp. 933-935
-
-
Abid, M.1
Teixeira, L.2
Török, B.3
-
33
-
-
0001911101
-
Esters of α-amino-α-arylΒ, Β, Β- trifluoroethanephosphonic acids
-
Markovskii LN, Shermolovich YG, Barashenkov GG, Kukhar VP, Soloshonok VA, Rozhenko AB. Esters of α-amino-α-arylΒ, Β, Β-trifluoroethanephosphonic acids. Zh. Obshch. Khim. 60, 2244-2247 (1990).
-
(1990)
Zh. Obshch. Khim.
, vol.60
, pp. 2244-2247
-
-
Markovskii, L.N.1
Shermolovich, Y.G.2
Barashenkov, G.G.3
Kukhar, V.P.4
Soloshonok, V.A.5
Rozhenko, A.B.6
-
34
-
-
61349197676
-
Recent Progress on the Stereoselective Synthesis of Cyclic Quaternary α-amino Acids
-
Cativiela C, Ordez M. Recent Progress on the Stereoselective Synthesis of Cyclic Quaternary α-amino Acids. Tetrahedron: Asymmetry 20, 1-63 (2009).
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 1-63
-
-
Cativiela, C.1
Ordez, M.2
-
35
-
-
0000500509
-
Fluorinecontaining amino acids. Vi. Acid-base properties of α-trifluoromethyl-α-amino acids
-
Kobzev SV, Soloshonok VA, Galushko SV, Yagupolskii YL, Kukhar VP. Fluorinecontaining amino acids. Vi. Acid-base properties of α- trifluoromethyl-α-amino acids. Zh. Obshch. Khim. 59, 909-912 (1989).
-
(1989)
Zh. Obshch. Khim.
, vol.59
, pp. 909-912
-
-
Kobzev, S.V.1
Soloshonok, V.A.2
Galushko, S.V.3
Yagupolskii, Y.L.4
Kukhar, V.P.5
-
36
-
-
0001850598
-
High-performance liquid chromatography of fluorine-containing amino acids
-
Kukhar VP, Soloshonok VA (Eds). John Wiley & Sons, Chichester, UK
-
Galushko SV. High-performance liquid chromatography of fluorine-containing amino acids. In: Fluorine-Containing Amino Acids. Kukhar VP, Soloshonok VA (Eds). John Wiley & Sons, Chichester, UK, 295-309 (1995).
-
(1995)
Fluorine-Containing Amino Acids
, pp. 295-309
-
-
Galushko, S.V.1
-
37
-
-
0343448040
-
Determination of enantiomeric composition of α-trifluoromethyl- α-amino acids by ligand-exchange microcolumn chromatography
-
Galushko SV, Shishkina IP, Kobzev SP, Soloshonok VA, Yagupolskii YL, Kukhar VP. Determination of enantiomeric composition of α-trifluoromethyl- α-amino acids by ligand-exchange microcolumn chromatography. Zh. Anal. Khim. 43, 2067-2069 (1988).
-
(1988)
Zh. Anal. Khim.
, vol.43
, pp. 2067-2069
-
-
Galushko, S.V.1
Shishkina, I.P.2
Kobzev, S.P.3
Soloshonok, V.A.4
Yagupolskii, Y.L.5
Kukhar, V.P.6
-
38
-
-
0025334175
-
Ligand-exchange chromatography of α-trifluoromethyl-α-amino acids on chiral sorbents
-
Galushko SV, Shishkina IP, Soloshonok VA, Kukhar VP. Ligand-exchange chromatography of α-trifluoromethyl-α-amino acids on chiral sorbents. J. Chromatogr. 511, 115-121 (1990).
-
(1990)
J. Chromatogr.
, vol.511
, pp. 115-121
-
-
Galushko, S.V.1
Shishkina, I.P.2
Soloshonok, V.A.3
Kukhar, V.P.4
-
39
-
-
0026514092
-
High-performance ligand-exchange chromatography of some amino acids containing two chiral centers
-
Galushko SV, Shishkina IP, Soloshonok VA. High-performance ligand-exchange chromatography of some amino acids containing two chiral centers. J. Chromatogr. 592, 345-348 (1992).
-
(1992)
J. Chromatogr.
, vol.592
, pp. 345-348
-
-
Galushko, S.V.1
Shishkina, I.P.2
Soloshonok, V.A.3
-
40
-
-
0001850598
-
Synthesis of Β-fluorinecontaining amino acids
-
Kukhar VP, Soloshonok VA (Eds). John Wiley & Sons, Chichester, UK
-
Sewald N, Burger K. Synthesis of Β-fluorinecontaining amino acids. In: Fluorine- Containing Amino Acids. Kukhar VP, Soloshonok VA (Eds). John Wiley & Sons, Chichester, UK, 295-309 (1995).
-
(1995)
Fluorine- Containing Amino Acids
, pp. 295-309
-
-
Sewald, N.1
Burger, K.2
-
41
-
-
0001714744
-
Derivatives of trifluoromethyl malic acid and their reactions
-
Soloshonok VA, Yagupolskii YL, Kukhar VP. Derivatives of trifluoromethyl malic acid and their reactions. Zh. Org. Khim. 23, 2523-2527 (1989).
-
(1989)
Zh. Org. Khim.
, vol.23
, pp. 2523-2527
-
-
Soloshonok, V.A.1
Yagupolskii, Y.L.2
Kukhar, V.P.3
-
42
-
-
0006634048
-
α-trifluoromethyl-α-hydroxy carboxylic acids
-
Soloshonok VA, Gerus II, Yagupolskii YL, Kukhar VP. α- trifluoromethyl-α-hydroxy carboxylic acids. Zh. Org. Khim. 23, 1441-1447 (1987).
-
(1987)
Zh. Org. Khim.
, vol.23
, pp. 1441-1447
-
-
Soloshonok, V.A.1
Gerus, I.I.2
Yagupolskii, Y.L.3
Kukhar, V.P.4
-
43
-
-
0000768436
-
Reactions of methyl trifluoropyruvate with terminal olefins
-
Soloshonok VA, Rozhenko AB, Butovich IA, Kukhar VP. Reactions of methyl trifluoropyruvate with terminal olefins. Zh. Org. Khim. 26, 2051-2056 (1990).
-
(1990)
Zh. Org. Khim.
, vol.26
, pp. 2051-2056
-
-
Soloshonok, V.A.1
Rozhenko, A.B.2
Butovich, I.A.3
Kukhar, V.P.4
-
44
-
-
0025874804
-
The unusual action of (R,S)-2-hydroxy-2- trifluoromethyl-trans-n-octadec- 4-enoic acid on 5-lipoxygenase from potato tubers
-
Butovich IA, Soloshonok VA, Kukhar VP. The unusual action of (R,S)-2-hydroxy-2- trifluoromethyl-trans-n-octadec-4-enoic acid on 5-lipoxygenase from potato tubers. Eur. J. Biochem. 199, 153-155 (1991).
-
(1991)
Eur. J. Biochem.
, vol.199
, pp. 153-155
-
-
Butovich, I.A.1
Soloshonok, V.A.2
Kukhar, V.P.3
-
45
-
-
0025377813
-
Activation of 5-lipoxygenase by lipophilic n-alkyl-containing acids is an allosteric process
-
Butovich IA, Soloshonok VA, Solodenko VA, Kukhar VP. Activation of 5-lipoxygenase by lipophilic n-alkyl-containing acids is an allosteric process. Bioorg. Khim. 16, 270-271 (1990).
-
(1990)
Bioorg. Khim.
, vol.16
, pp. 270-271
-
-
Butovich, I.A.1
Soloshonok, V.A.2
Solodenko, V.A.3
Kukhar, V.P.4
-
46
-
-
0001588790
-
Azomethine-azomethine isomerization of fluorinated n-benzylimines
-
Soloshonok VA, Gerus II, Yagupolskii YL, Kukhar VP. Azomethine-azomethine isomerization of fluorinated n-benzylimines. Zh. Org. Khim. 24, 993-997 (1988).
-
(1988)
Zh. Org. Khim.
, vol.24
, pp. 993-997
-
-
Soloshonok, V.A.1
Gerus, I.I.2
Yagupolskii, Y.L.3
Kukhar, V.P.4
-
47
-
-
0028279687
-
Practical rout to fluoroalkyl- and fluoroarylamines by base-catalyzed (1,3)-proton shift reaction
-
Soloshonok VA, Kirilenko AG, Kukhar VP, Resnati GA. Practical rout to fluoroalkyl- and fluoroarylamines by base-catalyzed (1,3)-proton shift reaction. Tetrahedron Lett. 35, 3119-3122 (1994).
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 3119-3122
-
-
Soloshonok, V.A.1
Kirilenko, A.G.2
Kukhar, V.P.3
Resnati, G.A.4
-
48
-
-
0001093043
-
Biomimetic reductive amination of fluoroaldehydes and ketones via [1,3]-proton shift reaction: Scope and limitations
-
Ono T, Kukhar VP, Soloshonok VA. Biomimetic reductive amination of fluoroaldehydes and ketones via [1,3]-proton shift reaction: scope and limitations. J. Org. Chem. 61, 6563-6569 (1996).
-
(1996)
J. Org. Chem.
, vol.61
, pp. 6563-6569
-
-
Ono, T.1
Kukhar, V.P.2
Soloshonok, V.A.3
-
49
-
-
0037430440
-
Simple and highly diastereoselective synthesis of trifluoromethyl- containing myosmines via reaction between 2-(aminomethyl)pyridine and 1,1,1,5,5,5-hexafluoro-2,4-pentanedione
-
Ohkura H, Berbasov DO, Soloshonok VA. Simple and highly diastereoselective synthesis of trifluoromethyl-containing myosmines via reaction between 2-(aminomethyl)pyridine and 1,1,1,5,5,5-hexafluoro-2,4- pentanedione. Tetrahedron Lett. 44, 2417-2420 (2003).
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 2417-2420
-
-
Ohkura, H.1
Berbasov, D.O.2
Soloshonok, V.A.3
-
50
-
-
33646520832
-
Novel sequence of two base-catalyzed 1,3 proton shifts and [12] wittig rearrangement in the synthesis of 2,4-bis-(trifluoromethyl)- phenylpyridine
-
Soloshonok VA, Ohkura H, Yasumoto M. Novel sequence of two base-catalyzed 1,3 proton shifts and [1,2] wittig rearrangement in the synthesis of 2,4-bis-(trifluoromethyl)- phenylpyridine. J. Fluor. Chem. 127, 708-711 (2006).
-
(2006)
J. Fluor. Chem.
, vol.127
, pp. 708-711
-
-
Soloshonok, V.A.1
Ohkura, H.2
Yasumoto, M.3
-
51
-
-
33745200707
-
Simple and convenient synthesis of 3,5-bis- (trifluoromethyl)benzylamine via 1,3-proton shift reaction
-
Soloshonok VA, Yasumoto M. Simple and convenient synthesis of 3,5-bis- (trifluoromethyl)benzylamine via 1,3-proton shift reaction. J. Fluor. Chem. 127, 889-893 (2006).
-
(2006)
J. Fluor. Chem.
, vol.127
, pp. 889-893
-
-
Soloshonok, V.A.1
Yasumoto, M.2
-
52
-
-
34250767148
-
Base-free, thermal 1,3-proton shift reaction and its application for operationally convenient and improved synthesis of α-(trifluoromethyl) benzylamine
-
Yasumoto M, Ueki H, Soloshonok VA. Base-free, thermal 1,3-proton shift reaction and its application for operationally convenient and improved synthesis of α-(trifluoromethyl)benzylamine. J. Fluor. Chem. 128, 736-739 (2007).
-
(2007)
J. Fluor. Chem.
, vol.128
, pp. 736-739
-
-
Yasumoto, M.1
Ueki, H.2
Soloshonok, V.A.3
-
53
-
-
0002601222
-
The effect of substituents on the feasibility of [1,3]-proton shift reaction: New synthetic opportunities
-
Soloshonok VA, Ono T. The effect of substituents on the feasibility of [1,3]-proton shift reaction: new synthetic opportunities. Synlett 919-921 (1996).
-
(1996)
Synlett
, pp. 919-921
-
-
Soloshonok, V.A.1
Ono, T.2
-
54
-
-
0030592749
-
The effect of substituents on the feasibility of azomethineazomethine isomerization: New synthetic opportunities for biomimetic transamination
-
Soloshonok VA, Ono T. The effect of substituents on the feasibility of azomethineazomethine isomerization: new synthetic opportunities for biomimetic transamination. Tetrahedron 52, 14701-14712 (1996).
-
(1996)
Tetrahedron
, vol.52
, pp. 14701-14712
-
-
Soloshonok, V.A.1
Ono, T.2
-
55
-
-
0030945696
-
Biomimetic transamination of α-keto perfluorocarboxylic esters. An efficient preparative synthesis of Β,Β,Β-trifluoroalanine
-
Soloshonok VA, Kukhar VP. Biomimetic transamination of α-keto perfluorocarboxylic esters. An efficient preparative synthesis of Β,Β,Β-trifluoroalanine. Tetrahedron 53, 8307-8314 (1997).
-
(1997)
Tetrahedron
, vol.53
, pp. 8307-8314
-
-
Soloshonok, V.A.1
Kukhar, V.P.2
-
56
-
-
0037416951
-
Chemo-and regioselectivity in the reactions between highly electrophilic fluorine containing dicarbonyl compounds and amines. Improved synthesis of the corresponding imines/enamines
-
Ohkura H, Berbasov DO, Soloshonok VA. Chemo- and regioselectivity in the reactions between highly electrophilic fluorine containing dicarbonyl compounds and amines. Improved synthesis of the corresponding imines/enamines. Tetrahedron 59, 1647-1656 (2003).
-
(2003)
Tetrahedron
, vol.59
, pp. 1647-1656
-
-
Ohkura, H.1
Berbasov, D.O.2
Soloshonok, V.A.3
-
57
-
-
2342514097
-
Synthesis of highly 1,3-proton-shifttransferable n-benzyl imines of trifluoroacetophenone under the 'low-basicity' reaction conditions
-
Berbasov DO, Ojemaye ID, Soloshonok VA. Synthesis of highly 1,3-proton-shifttransferable n-benzyl imines of trifluoroacetophenone under the 'low-basicity' reaction conditions. J. Fluor. Chem. 125, 603-607 (2004).
-
(2004)
J. Fluor. Chem.
, vol.125
, pp. 603-607
-
-
Berbasov, D.O.1
Ojemaye, I.D.2
Soloshonok, V.A.3
-
58
-
-
10044249880
-
Synthesis of fluorine-containing compounds under operationally convenient conditions
-
Soloshonok VA, Berbasov DO. Synthesis of fluorine-containing compounds under operationally convenient conditions. J. Fluor. Chem. 125, 1757-1763 (2004).
-
(2004)
J. Fluor. Chem.
, vol.125
, pp. 1757-1763
-
-
Soloshonok, V.A.1
Berbasov, D.O.2
-
60
-
-
0027156061
-
Transamination of fluorinated Β-keto carboxylic esters. A biomimetic approach to Β-polyfluoroalkyl-Β-amino acids
-
Soloshonok VA, Kirilenko AG, Kukhar VP, Resnati G. Transamination of fluorinated Β-keto carboxylic esters. A biomimetic approach to Β-polyfluoroalkyl-Β-amino acids. Tetrahedron Lett. 34, 3621-3624 (1993).
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 3621-3624
-
-
Soloshonok, V.A.1
Kirilenko, A.G.2
Kukhar, V.P.3
Resnati, G.4
-
61
-
-
0029969511
-
Biomimetic base-catalyzed [1,3]-proton shift reaction. A practical synthesis of Β-fluoroalkyl-Β-amino acids
-
Soloshonok VA, Kukhar VP. Biomimetic base-catalyzed [1,3]-proton shift reaction. A practical synthesis of Β-fluoroalkyl-Β-amino acids. Tetrahedron 52, 6953-6964 (1996).
-
(1996)
Tetrahedron
, vol.52
, pp. 6953-6964
-
-
Soloshonok, V.A.1
Kukhar, V.P.2
-
62
-
-
0037194189
-
Reducing reagent-free, biomimetic reductive amination of perfluorocarboxylic acids to α, α-dihydroperfluoroamines
-
Soloshonok VA, Ohkura H, Uneyama K. Reducing reagent-free, biomimetic reductive amination of perfluorocarboxylic acids to α, α-dihydroperfluoroamines. Tetrahedron Lett. 43, 5449-5452 (2002).
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 5449-5452
-
-
Soloshonok, V.A.1
Ohkura, H.2
Uneyama, K.3
-
63
-
-
0000647037
-
Asymmetric [1,3]-proton shift in azomethines as a new approach to the synthesis of optically active α-trifluoromethyl-containing amines and amino acids
-
Kukhar VP, Soloshonok VS, Galushko SV, Rozhenko AB. Asymmetric [1,3]-proton shift in azomethines as a new approach to the synthesis of optically active α-trifluoromethyl-containing amines and amino acids. Dokl. Akad. Nauk SSSR 310, 886-889 (1990).
-
(1990)
Dokl. Akad. Nauk SSSR
, vol.310
, pp. 886-889
-
-
Kukhar, V.P.1
Soloshonok, V.S.2
Galushko, S.V.3
Rozhenko, A.B.4
-
64
-
-
0030916859
-
Highly enantioselective transfer of chirality from a less to a more conformationally unstable stereogenic center. A practical asymmetric synthesis of perfluoroalkyl amines
-
Soloshonok VA, Ono T. Highly enantioselective transfer of chirality from a less to a more conformationally unstable stereogenic center. A practical asymmetric synthesis of perfluoroalkyl amines. J. Org. Chem. 62, 3030-3031 (1997).
-
(1997)
J. Org. Chem.
, vol.62
, pp. 3030-3031
-
-
Soloshonok, V.A.1
Ono, T.2
-
65
-
-
33746918968
-
Unusual condensation of 1,1,1,5,5,5-hexafluoro-2,4-pentanedione with (R)-phenylglycinol
-
Soloshonok VA, Ohkura H, Yasumoto M. Unusual condensation of 1,1,1,5,5,5-hexafluoro-2,4-pentanedione with (R)-phenylglycinol. Mendeleev Commun. 165-167 (2006).
-
(2006)
Mendeleev Commun
, pp. 165-167
-
-
Soloshonok, V.A.1
Ohkura, H.2
Yasumoto, M.3
-
66
-
-
0001462375
-
Enantioselective biomimetic transamination of α-keto carboxylic acid derivatives. An efficient asymmetric synthesis of Β-fluoroalkyl- Β-amino acids
-
Soloshonok VA, Ono T, Soloshonok IV. Enantioselective biomimetic transamination of α-keto carboxylic acid derivatives. An efficient asymmetric synthesis of Β-fluoroalkyl-Β-amino acids. J. Org. Chem. 62, 7538-7539 (1997).
-
(1997)
J. Org. Chem.
, vol.62
, pp. 7538-7539
-
-
Soloshonok, V.A.1
Ono, T.2
Soloshonok, I.V.3
-
67
-
-
33745200248
-
Operationally convenient asymmetric synthesis of (S)-and (R)-3-amino-4,4,4- trifluorobutanoic acid. Part I: Enantioselective biomimetic transamination of isopropyl 4,4,4-trifluoro-3-oxobutanoate
-
Soloshonok VA, Ohkura H, Yasumoto M. Operationally convenient asymmetric synthesis of (S)- and (R)-3-amino-4,4,4- trifluorobutanoic acid. Part I: enantioselective biomimetic transamination of isopropyl 4,4,4-trifluoro-3- oxobutanoate. J. Fluor. Chem. 127, 924-929 (2006).
-
(2006)
J. Fluor. Chem.
, vol.127
, pp. 924-929
-
-
Soloshonok, V.A.1
Ohkura, H.2
Yasumoto, M.3
-
68
-
-
33745197089
-
Operationally convenient asymmetric synthesis of (S)- and (R)-3-amino-4,4,4- trifluorobutanoic acid. Part II: Enantioselective biomimetic transamination of 4,4,4-trifluoro-3-oxo-N-[(R)-1- phenylethyl)butanamide
-
Soloshonok VA, Ohkura H, Yasumoto M. Operationally convenient asymmetric synthesis of (S)- and (R)-3-amino-4,4,4- trifluorobutanoic acid. Part II: enantioselective biomimetic transamination of 4,4,4-trifluoro-3-oxo-N-[(R)-1- phenylethyl)butanamide. J. Fluor. Chem. 127, 930-935 (2006).
-
(2006)
J. Fluor. Chem.
, vol.127
, pp. 930-935
-
-
Soloshonok, V.A.1
Ohkura, H.2
Yasumoto, M.3
-
69
-
-
0028237842
-
Catalytic asymmetric synthesis of Β-fluoroalkyl-Β-amino acids via biomimetic [1,3]-proton shift reaction
-
Soloshonok VA, Kirilenko AG, Galushko SV, Kukhar VP. Catalytic asymmetric synthesis of Β-fluoroalkyl-Β-amino acids via biomimetic [1,3]-proton shift reaction. Tetrahedron Lett. 35, 5063-5064 (1994).
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 5063-5064
-
-
Soloshonok, V.A.1
Kirilenko, A.G.2
Galushko, S.V.3
Kukhar, V.P.4
-
70
-
-
33846821373
-
Catalytic asymmetric synthesis of α-(trifluoromethyl) benzylamine via cinchonidine derived base-catalyzed biomimetic 1,3-proton shift reaction
-
Soloshonok VA, Yasumoto M. Catalytic asymmetric synthesis of α-(trifluoromethyl) benzylamine via cinchonidine derived base-catalyzed biomimetic 1,3-proton shift reaction. J. Fluor. Chem. 128, 170-173 (2007).
-
(2007)
J. Fluor. Chem.
, vol.128
, pp. 170-173
-
-
Soloshonok, V.A.1
Yasumoto, M.2
-
71
-
-
50549091408
-
First example of continuous-flow reaction conditions for biomimetic reductive amination of fluorine-containing carbonyl compounds
-
Soloshonok VA, Ono T. First example of continuous-flow reaction conditions for biomimetic reductive amination of fluorine-containing carbonyl compounds. J. Fluor. Chem. 129, 785-787 (2008).
-
(2008)
J. Fluor. Chem.
, vol.129
, pp. 785-787
-
-
Soloshonok, V.A.1
Ono, T.2
-
72
-
-
67349254163
-
Continuous-flow asymmetric biomimetic transamination
-
Soloshonok VA, Catt HT, Ono T. Continuous-flow asymmetric biomimetic transamination. J. Fluor. Chem. 130, 512-515 (2009).
-
(2009)
J. Fluor. Chem.
, vol.130
, pp. 512-515
-
-
Soloshonok, V.A.1
Catt, H.T.2
Ono, T.3
-
73
-
-
0000662243
-
Kinetics and mechanism of the isomerization of N-(1-methoxycarbonyl- 2,2,2-trifluoroethylidene)-α-methylbenzylamine
-
Khotkevich AB, Soloshonok VA, Yagupolskii YL. Kinetics and mechanism of the isomerization of N-(1-methoxycarbonyl- 2,2,2-trifluoroethylidene)-α- methylbenzylamine. Zh. Obshch. Khim. 60, 1005-1008 (1990).
-
(1990)
Zh. Obshch. Khim.
, vol.60
, pp. 1005-1008
-
-
Khotkevich, A.B.1
Soloshonok, V.A.2
Yagupolskii, Y.L.3
-
74
-
-
42049113008
-
Kinetics and mechanism of triethylamine-catalyzed 1,3-proton shift. Optimized and substantially improved reaction conditions for biomimetic reductive amination of fluorine-containing carbonyl compounds
-
Nagy P, Ueki H, Berbasov DO, Soloshonok VA. Kinetics and mechanism of triethylamine-catalyzed 1,3-proton shift. Optimized and substantially improved reaction conditions for biomimetic reductive amination of fluorine-containing carbonyl compounds. J. Fluor. Chem. 129, 409-415 (2008).
-
(2008)
J. Fluor. Chem.
, vol.129
, pp. 409-415
-
-
Nagy, P.1
Ueki, H.2
Berbasov, D.O.3
Soloshonok, V.A.4
-
76
-
-
0028023232
-
Chemo-enzymatic approach to the synthesis of each of the four isomers of α-alkyl-Β-fluoroalkyl-substituted Β-amino acids
-
Soloshonok VA, Kirilenko AG, Fokina NA et al. Chemo-enzymatic approach to the synthesis of each of the four isomers of α-alkyl-Β-fluoroalkyl- substituted Β-amino acids. Tetrahedron: Asymmetry 5, 1225-1228 (1994).
-
(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 1225-1228
-
-
Soloshonok, V.A.1
Kirilenko, A.G.2
Fokina, N.A.3
-
78
-
-
0001534452
-
Biomimetic transamination of α-alkyl-Β-keto carboxylic esters. Chemoenzymatic approach to the stereochemically defined α-alkyl-Β- fluoroalkyl-Β-amino acids
-
Soloshonok VA, Soloshonok IV, Kukhar VP, Svedas VK. Biomimetic transamination of α-alkyl-Β-keto carboxylic esters. Chemoenzymatic approach to the stereochemically defined α-alkyl-Β-fluoroalkyl- Β-amino acids. J. Org. Chem. 63, 1878-1884 (1998).
-
(1998)
J. Org. Chem.
, vol.63
, pp. 1878-1884
-
-
Soloshonok, V.A.1
Soloshonok, I.V.2
Kukhar, V.P.3
Svedas, V.K.4
-
79
-
-
31444451709
-
Remarkable amplification of self-disproportionation of enantiomers on achiral-phase chromatography columns
-
Soloshonok VA. Remarkable amplification of self-disproportionation of enantiomers on achiral-phase chromatography columns. Angew. Chem. Int. Ed. Engl. 45, 766-769 (2006).
-
(2006)
Angew. Chem. Int. Ed. Engl.
, vol.45
, pp. 766-769
-
-
Soloshonok, V.A.1
-
80
-
-
33745192709
-
Selfdisproportionation of enantiomers of (R)-ethyl 3-(3,5- dinitrobenzamido)-4,4,4- trifluorobutanoate on achiral silica gel stationary phase
-
Soloshonok VA, Berbasov DO. Selfdisproportionation of enantiomers of (R)-ethyl 3-(3,5-dinitrobenzamido)-4,4,4- trifluorobutanoate on achiral silica gel stationary phase. J. Fluor. Chem. 127, 597-603 (2006).
-
(2006)
J. Fluor. Chem.
, vol.127
, pp. 597-603
-
-
Soloshonok, V.A.1
Berbasov, D.O.2
-
81
-
-
33846839754
-
Selfdisproportionation of enantiomers on achiral phase chromatography. One more example of fluorine's magic powers
-
Soloshonok VA, Berbasov DO. Selfdisproportionation of enantiomers on achiral phase chromatography. One more example of fluorine's magic powers. Chem. Today 24, 44-47 (2006).
-
(2006)
Chem. Today
, vol.24
, pp. 44-47
-
-
Soloshonok, V.A.1
Berbasov, D.O.2
-
82
-
-
35048842717
-
Phenomenon of optical self-purification of chiral non-racemic compounds
-
Soloshonok VA, Ueki H, Yasumoto M, Mekala S, Hirschi JS, Singleton DA. Phenomenon of optical self-purification of chiral non-racemic compounds. J. Am. Chem. Soc. 129, 12112-12113 (2007).
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 12112-12113
-
-
Soloshonok, V.A.1
Ueki, H.2
Yasumoto, M.3
Mekala, S.4
Hirschi, J.S.5
Singleton, D.A.6
-
83
-
-
65249106731
-
New sterically driven mode for generation of helical chirality
-
Ueki H, Soloshonok VA. New sterically driven mode for generation of helical chirality. Org. Lett. 11, 1797 - 1800 (2009).
-
(2009)
Org. Lett.
, vol.11
, pp. 1797-1800
-
-
Ueki, H.1
Soloshonok, V.A.2
-
88
-
-
65249131138
-
Recent advances in the chemistry and biology of new generation taxoids
-
Ojima I, Das M. Recent advances in the chemistry and biology of new generation taxoids. J. Nat. Prod. 72, 554-565 (2008).
-
(2008)
J. Nat. Prod.
, vol.72
, pp. 554-565
-
-
Ojima, I.1
Das, M.2
-
89
-
-
0028329208
-
Gold(I)-catalyzed asymmetric aldol reaction of methyl isocyanoacetate with fluorinated benzaldehydes
-
Soloshonok VA, Hayashi T. Gold(I)-catalyzed asymmetric aldol reaction of methyl isocyanoacetate with fluorinated benzaldehydes. Tetrahedron Lett. 35, 2713-2716 (1994).
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 2713-2716
-
-
Soloshonok, V.A.1
Hayashi, T.2
-
90
-
-
0028307422
-
Gold(I)-catalyzed asymmetric aldol reaction of fluorinated benzaldehydes with α-isocyanoacetamide
-
Soloshonok VA, Hayashi T. Gold(I)-catalyzed asymmetric aldol reaction of fluorinated benzaldehydes with α-isocyanoacetamide. Tetrahedron: Asymmetry 5, 1091-1094 (1994).
-
(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 1091-1094
-
-
Soloshonok, V.A.1
Hayashi, T.2
-
91
-
-
0029655532
-
Gold(I)-catalyzed asymmetric aldol reactions of isocyanoacetic acid derivatives with fluoroaryl aldehydes
-
Soloshonok VA, Kacharov AD, Hayashi T. Gold(I)-catalyzed asymmetric aldol reactions of isocyanoacetic acid derivatives with fluoroaryl aldehydes. Tetrahedron 52, 245-254 (1996).
-
(1996)
Tetrahedron
, vol.52
, pp. 245-254
-
-
Soloshonok, V.A.1
Kacharov, A.D.2
Hayashi, T.3
-
92
-
-
33845376099
-
Catalytic asymmetric aldol reaction: Reaction of aldehydes with isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complex
-
Ito Y, Sawamura M, Hayashi T. Catalytic asymmetric aldol reaction: reaction of aldehydes with isocyanoacetate catalyzed by a chiral ferrocenylphosphine-gold(I) complex. J. Am. Chem. Soc. 108, 6405-6406 (1986).
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 6405-6406
-
-
Ito, Y.1
Sawamura, M.2
Hayashi, T.3
-
93
-
-
0030575363
-
Erythro-selective aldol-type reaction of N-sulfonylaldimines with methyl isocyanoacetate catalyzed by gold(I)
-
Hayashi T, Kishi E, Soloshonok VA, Uozumi Y. Erythro-selective aldol-type reaction of N-sulfonylaldimines with methyl isocyanoacetate catalyzed by gold(I). Tetrahedron Lett. 37, 4969-4972 (1996).
-
(1996)
Tetrahedron Lett
, pp. 4969-4972
-
-
Hayashi, T.1
Kishi, E.2
Soloshonok, V.A.3
Uozumi, Y.4
-
94
-
-
0028258252
-
Highly diastereoselective aldol reaction of fluoroalkyl aryl ketones with methyl isocyanoacetate catalyzed by silver(I)/ triethylamine
-
Soloshonok VA, Hayashi T, Ishikawa K, Nagashima N. Highly diastereoselective aldol reaction of fluoroalkyl aryl ketones with methyl isocyanoacetate catalyzed by silver(I)/ triethylamine. Tetrahedron Lett. 35, 1055-1058 (1994).
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 1055-1058
-
-
Soloshonok, V.A.1
Hayashi, T.2
Ishikawa, K.3
Nagashima, N.4
-
95
-
-
0030597177
-
Transition metal-catalyzed diastereoselective aldol reactions of prochiral ketones with methyl isocyanoacetate
-
Soloshonok VA, Kacharov AD, Avilov DV, Hayashi T. Transition metal-catalyzed diastereoselective aldol reactions of prochiral ketones with methyl isocyanoacetate. Tetrahedron Lett. 37, 7845-7848 (1996).
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 7845-7848
-
-
Soloshonok, V.A.1
Kacharov, A.D.2
Avilov, D.V.3
Hayashi, T.4
-
96
-
-
0000857641
-
Transition metal/base-catalyzed aldol reactions of methyl α-isocyanoacetate with prochiral ketones, a straightforward approach to stereochemically defined Β, Β-disubstitutedΒ- hydroxy-α-amino acids. Scope and limitations
-
Soloshonok VA, Kacharov AD, Avilov DV, Ishikawa K, Nagashima N, Hayashi T. Transition metal/base-catalyzed aldol reactions of methyl α-isocyanoacetate with prochiral ketones, a straightforward approach to stereochemically defined Β, Β-disubstitutedΒ- hydroxy-α-amino acids. Scope and limitations. J. Org. Chem. 62, 3470-3479 (1997).
-
(1997)
J. Org. Chem.
, vol.62
, pp. 3470-3479
-
-
Soloshonok, V.A.1
Kacharov, A.D.2
Avilov, D.V.3
Ishikawa, K.4
Nagashima, N.5
Hayashi, T.6
-
97
-
-
0042338452
-
Improved synthesis of proline derived Ni(ii)-complexes of glycine, a versatile chiral equivalents of nucleophilic glycine for general asymmetric synthesis of α-amino acids
-
Ueki H, Ellis TK, Martin CH, Bolene SB, Boettiger TU, Soloshonok VA. Improved synthesis of proline derived Ni(ii)-complexes of glycine, a versatile chiral equivalents of nucleophilic glycine for general asymmetric synthesis of α-amino acids. J. Org. Chem. 68, 7104-7107 (2003).
-
(2003)
J. Org. Chem.
, vol.68
, pp. 7104-7107
-
-
Ueki, H.1
Ellis, T.K.2
Martin, C.H.3
Bolene, S.B.4
Boettiger, T.U.5
Soloshonok, V.A.6
-
98
-
-
0027473427
-
Asymmetric synthesis of organoelement analogs of natural products. Part 12. General method for the asymmetric synthesis of fluorine-containing phenylalanines and α-methylphenylalanines via alkylation of the chiral nickel(ii) Schiff 's base complexes of glycine and alanine
-
Kukhar VP, Belokon YN, Svistunova NY, Soloshonok VA, Rozhenko AB, Kuzmina NA. Asymmetric synthesis of organoelement analogs of natural products. Part 12. General method for the asymmetric synthesis of fluorine-containing phenylalanines and α-methylphenylalanines via alkylation of the chiral nickel(ii) Schiff 's base complexes of glycine and alanine. Synthesis 117-121 (1993).
-
(1993)
Synthesis
, pp. 117-121
-
-
Kukhar, V.P.1
Belokon, Y.N.2
Svistunova, N.Y.3
Soloshonok, V.A.4
Rozhenko, A.B.5
Kuzmina, N.A.6
-
99
-
-
0035825745
-
Asymmetric synthesis of α,Β-dialkyl-αphenylalanines via direct alkylation of chiral alanine derivative with racemic α- alkylbenzylbromides. A case of high enantiomer differentiation at room temperature
-
Soloshonok VA, Tang X, Hruby VJ, Meervelt LV. Asymmetric synthesis of α,Β-dialkyl-αphenylalanines via direct alkylation of chiral alanine derivative with racemic α-alkylbenzylbromides. A case of high enantiomer differentiation at room temperature. Org. Letters 3, 341-343 (2001).
-
(2001)
Org. Letters
, vol.3
, pp. 341-343
-
-
Soloshonok, V.A.1
Tang, X.2
Hruby, V.J.3
Meervelt, L.V.4
-
100
-
-
50849122696
-
Asymmetric synthesis of (2S,3S)- and (2R,3R)-α,Β-dialkyl- α-amino acids via alkylation of chiral Ni(ii)-complexes of aliphatic α-amino acids with racemic α-alkylbenzylbromides
-
Soloshonok VA, Boettiger TU, Bolene SB. Asymmetric synthesis of (2S,3S)- and (2R,3R)-α,Β-dialkyl-α-amino acids via alkylation of chiral Ni(ii)-complexes of aliphatic α-amino acids with racemic α-alkylbenzylbromides. Synthesis 2594-2602 (2008).
-
(2008)
Synthesis
, pp. 2594-2602
-
-
Soloshonok, V.A.1
Boettiger, T.U.2
Bolene, S.B.3
-
101
-
-
67349086580
-
Operationally convenient asymmetric synthesis of (S)-2-amino-3,3-bis-(4- fluorophenyl) propanoic acid
-
Soloshonok VA, Ono T. Operationally convenient asymmetric synthesis of (S)-2-amino-3,3-bis-(4-fluorophenyl) propanoic acid. J. Fluor. Chem. 130, 547-549 (2009).
-
(2009)
J. Fluor. Chem.
, vol.130
, pp. 547-549
-
-
Soloshonok, V.A.1
Ono, T.2
-
102
-
-
33845248258
-
The next big thing in diabetes: Clinical progress on DPP-IV inhibitors
-
von Geldern TW, Trevillyan JM. The next big thing in diabetes: clinical progress on DPP-IV inhibitors. Drug Dev. Res. 67, 627-642 (2006).
-
(2006)
Drug Dev. Res.
, vol.67
, pp. 627-642
-
-
Von Geldern, T.W.1
Trevillyan, J.M.2
-
103
-
-
36349006502
-
Synthesis of 4-fluoro-Β-(4-fluorophenyl)-l-phenylalanine by an asymmetric phase-transfer catalyzed alkylation: Synthesis on scale and catalyst stability
-
Patterson DE, Xie S, Jones LA, Osterhout MH, Henry CG, Roper TD. Synthesis of 4-fluoro-Β-(4-fluorophenyl)-l-phenylalanine by an asymmetric phase-transfer catalyzed alkylation: synthesis on scale and catalyst stability. Org. Process Res. Dev. 11, 624-627 (2007).
-
(2007)
Org. Process Res. Dev.
, vol.11
, pp. 624-627
-
-
Patterson, D.E.1
Xie, S.2
Jones, L.A.3
Osterhout, M.H.4
Henry, C.G.5
Roper, T.D.6
-
105
-
-
77953409599
-
Asymmetric synthesis of organoelement analogs of natural products. 6. (S)-α-aminoω- phosphonocarboxylic acids
-
Soloshonok VA, Svistunova NY, Kukhar VP et al. Asymmetric synthesis of organoelement analogs of natural products. 6. (S)-α-aminoω- phosphonocarboxylic acids. Izv. Akad. Nauk SSSR Ser. Khim. 397-402 (1992).
-
(1992)
Izv. Akad. Nauk SSSR Ser. Khim.
, pp. 397-402
-
-
Soloshonok, V.A.1
Svistunova, N.Y.2
Kukhar, V.P.3
-
106
-
-
0022617694
-
Inhibition of Escherichia coli glutamine synthetase by phosphinothricin
-
Colanduoni JA, Villafranca JJ. Inhibition of Escherichia coli glutamine synthetase by phosphinothricin. Bioorg. Chem. 14, 163-169 (1986).
-
(1986)
Bioorg. Chem.
, vol.14
, pp. 163-169
-
-
Colanduoni, J.A.1
Villafranca, J.J.2
-
107
-
-
34249766509
-
Asymmetric synthesis of organoelement analogs of natural products. 17. Fluorinecontaining esters of (S)-homocysteic acid
-
Soloshonok VA, Svistunova NY, Kukhar VP et al. Asymmetric synthesis of organoelement analogs of natural products. 17. Fluorinecontaining esters of (S)-homocysteic acid. Russian Chem. Bull. 42, 755-759 (1993)
-
(1993)
Russian Chem. Bull.
, vol.42
, pp. 755-759
-
-
Soloshonok, V.A.1
Svistunova, N.Y.2
Kukhar, V.P.3
-
108
-
-
8544228333
-
Asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via methylenedimerization of chiral glycine equivalents with dichloromethane under operationally convenient conditions
-
Taylor SM, Yamada T, Ueki H, Soloshonok VA. Asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via methylenedimerization of chiral glycine equivalents with dichloromethane under operationally convenient conditions. Tetrahedron Lett. 45, 9159-9162 (2004).
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 9159-9162
-
-
Taylor, S.M.1
Yamada, T.2
Ueki, H.3
Soloshonok, V.A.4
-
109
-
-
33646804903
-
Operationally convenient, efficient asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via direct methylenedimerization of chiral glycine equivalents with dichloromethane
-
Soloshonok VA, Yamada T, Ueki H et al. Operationally convenient, efficient asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via direct methylenedimerization of chiral glycine equivalents with dichloromethane. Tetrahedron 62, 6412-6419 (2006).
-
(2006)
Tetrahedron
, vol.62
, pp. 6412-6419
-
-
Soloshonok, V.A.1
Yamada, T.2
Ueki, H.3
-
110
-
-
0023735973
-
Fluorine-containing amino acids and their derivatives. 7. Synthesis and antitumor activity of α- And γ-substituted methotrexate analogs
-
Tsushima T, Kawada K, Ishihara S et al. Fluorine-containing amino acids and their derivatives. 7. Synthesis and antitumor activity of α- and γ-substituted methotrexate analogs. Tetrahedron 44, 5375-5387 (1988).
-
(1988)
Tetrahedron
, vol.44
, pp. 5375-5387
-
-
Tsushima, T.1
Kawada, K.2
Ishihara, S.3
-
111
-
-
0036224968
-
Highly diastereoselective michael addition reactions between nucleophilic glycine equivalents and Β-substituted-α, Β-unsaturated carboxylic acid derivatives; A general approach to the stereochemically defined and sterically χ-constrained α-amino acids
-
Soloshonok VA. Highly diastereoselective michael addition reactions between nucleophilic glycine equivalents and Β-substituted-α,Β- unsaturated carboxylic acid derivatives; a general approach to the stereochemically defined and sterically χ-constrained α-amino acids. Curr. Org. Chem. 6, 341-364 (2002).
-
(2002)
Curr. Org. Chem.
, vol.6
, pp. 341-364
-
-
Soloshonok, V.A.1
-
112
-
-
1542725948
-
Biological and conformational study of α-substituted prolines in mt-ii template: Steric effects leading to human mc5 receptor selectivity
-
Cai M, Cai C, Mayorov AV et al. Biological and conformational study of α-substituted prolines in mt-ii template: steric effects leading to human mc5 receptor selectivity. J. Peptide Research 63, 116-131 (2004).
-
(2004)
J. Peptide Research
, vol.63
, pp. 116-131
-
-
Cai, M.1
Cai, C.2
Mayorov, A.V.3
-
113
-
-
0035939193
-
Largescale asymmetric synthesis of novel sterically constrained 2′,6prime;-dimethyl- and α,2′,6prime;- trimethyltyrosine and -phenylalanine derivatives via alkylation of chiral equivalents of nucleophilic glycine and alanine
-
Soloshonok VA, Tang X, Hruby VJ. Largescale asymmetric synthesis of novel sterically constrained 2′,6prime;-dimethyl- and α,2′,6prime;- trimethyltyrosine and -phenylalanine derivatives via alkylation of chiral equivalents of nucleophilic glycine and alanine. Tetrahedron 57, 6375-6382 (2001).
-
(2001)
Tetrahedron
, vol.57
, pp. 6375-6382
-
-
Soloshonok, V.A.1
Tang, X.2
Hruby, V.J.3
-
114
-
-
0034725677
-
Convenient asymmetric synthesis of enantiomerically pure 2′,6prime;-dimethyltyrosine (dmt) via alkylation of chiral nucleophilic glycine equivalent
-
Tang X, Soloshonok VA, Hruby VJ. Convenient asymmetric synthesis of enantiomerically pure 2′,6prime;-dimethyltyrosine (dmt) via alkylation of chiral nucleophilic glycine equivalent. Tetrahedron: Asymmetry 11, 2917-2925 (2000).
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 2917-2925
-
-
Tang, X.1
Soloshonok, V.A.2
Hruby, V.J.3
-
115
-
-
0034697001
-
Convenient, large-scale asymmetric synthesis of enantiomerically pure trans-cinnamylglycine and -α-alanine
-
Qiu W, Soloshonok VA, Cai C, Tang X, Hruby VJ. Convenient, large-scale asymmetric synthesis of enantiomerically pure trans-cinnamylglycine and -α-alanine. Tetrahedron 56, 2577-2582 (2000).
-
(2000)
Tetrahedron
, vol.56
, pp. 2577-2582
-
-
Qiu, W.1
Soloshonok, V.A.2
Cai, C.3
Tang, X.4
Hruby, V.J.5
-
116
-
-
0038277395
-
Efficient synthesis of 2-aminoindane-2- carboxylic acid via dialkylation of nucleophilic glycine equivalent
-
Ellis TK, Hochla VM, Soloshonok VA. Efficient synthesis of 2-aminoindane-2- carboxylic acid via dialkylation of nucleophilic glycine equivalent. J. Org. Chem. 68, 4973-4976 (2003).
-
(2003)
J. Org. Chem.
, vol.68
, pp. 4973-4976
-
-
Ellis, T.K.1
Hochla, V.M.2
Soloshonok, V.A.3
-
117
-
-
0037467867
-
Efficient, practical synthesis of symmetrically α,α- disubstituted α-amino acids
-
Ellis TK, Martin CH, Ueki H, Soloshonok VA. Efficient, practical synthesis of symmetrically α,α-disubstituted α-amino acids. Tetrahedron Lett. 44, 1063-1066 (2003).
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 1063-1066
-
-
Ellis, T.K.1
Martin, C.H.2
Ueki, H.3
Soloshonok, V.A.4
-
118
-
-
0043032849
-
Efficient synthesis of sterically constrained symmetrically α,α-disubstituted α-amino acids under operationally convenient conditions
-
Ellis TK, Martin CH, Tsai GM, Ueki H, Soloshonok VA. Efficient synthesis of sterically constrained symmetrically α,α-disubstituted α-amino acids under operationally convenient conditions. J. Org. Chem. 68, 6208-6214 (2003).
-
(2003)
J. Org. Chem.
, vol.68
, pp. 6208-6214
-
-
Ellis, T.K.1
Martin, C.H.2
Tsai, G.M.3
Ueki, H.4
Soloshonok, V.A.5
-
119
-
-
37049075389
-
General method for the synthesis of enantiomerically pure α-hydroxy-α-amino acids, containing fluorine atoms in the side chains. Case of stereochemical distinction between methyl and trifluoromethyl groups. X-ray crystal and molecular structure of the nickel(ii) complex of (2S,3S)-2- (trifluoromethyl)threonine
-
Soloshonok VA, Kukhar VP, Galushko SV et al. General method for the synthesis of enantiomerically pure α-hydroxy-α-amino acids, containing fluorine atoms in the side chains. Case of stereochemical distinction between methyl and trifluoromethyl groups. X-ray crystal and molecular structure of the nickel(ii) complex of (2S,3S)-2- (trifluoromethyl)threonine. J. Chem. Soc. Perkin Trans. 1, 3143-3155 (1993).
-
(1993)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 3143-3155
-
-
Soloshonok, V.A.1
Kukhar, V.P.2
Galushko, S.V.3
-
120
-
-
0029163546
-
Asymmetric aldol reactions of chiral ni(ii)-complex of glycine with aldehydes. Stereodivergent synthesis of syn-(2S)- and syn-(2R)-Β- alkylserines
-
Soloshonok VA, Avilov DV, Kukhar VP et al. Asymmetric aldol reactions of chiral ni(ii)-complex of glycine with aldehydes. Stereodivergent synthesis of syn-(2S)- and syn-(2R)-Β-alkylserines. Tetrahedron: Asymmetry 6, 1741-1756 (1995).
-
(1995)
Tetrahedron: Asymmetry
, vol.6
, pp. 1741-1756
-
-
Soloshonok, V.A.1
Avilov, D.V.2
Kukhar, V.P.3
-
121
-
-
0030961675
-
Highly diastereoselective aza-aldol reactions of a chiral ni(ii) complex of glycine with imines. An efficient asymmetric approach to 3-perfluoroalkyl-2, 3-diamino acids
-
Soloshonok VA, Avilov DV, Kukhar VP, Meervelt LV, Mischenko N. Highly diastereoselective aza-aldol reactions of a chiral ni(ii) complex of glycine with imines. An efficient asymmetric approach to 3-perfluoroalkyl-2,3-diamino acids. Tetrahedron Lett. 38, 4671-4674 (1997).
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 4671-4674
-
-
Soloshonok, V.A.1
Avilov, D.V.2
Kukhar, V.P.3
Meervelt, L.V.4
Mischenko, N.5
-
122
-
-
0029883406
-
Highly diastereoselective asymmetric aldol reactions of chiral Ni(ii)-complex of glycine with trifluoromethyl ketones
-
Soloshonok VA, Avilov DV, Kukhar VP. Highly diastereoselective asymmetric aldol reactions of chiral Ni(ii)-complex of glycine with trifluoromethyl ketones. Tetrahedron: Asymmetry 7, 1547-1550(1996).
-
(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 1547-1550
-
-
Soloshonok, V.A.1
Avilov, D.V.2
Kukhar, V.P.3
-
123
-
-
0030590464
-
Asymmetric aldol reactions of trifluoromethyl ketones with a chiral Ni(ii) complex of glycine: Stereocontrolling effect of the trifluoromethyl group
-
Soloshonok VA, Avilov DV, Kukhar VP. Asymmetric aldol reactions of trifluoromethyl ketones with a chiral Ni(ii) complex of glycine: stereocontrolling effect of the trifluoromethyl group. Tetrahedron 52, 12433-12442 (1996).
-
(1996)
Tetrahedron
, vol.52
, pp. 12433-12442
-
-
Soloshonok, V.A.1
Avilov, D.V.2
Kukhar, V.P.3
-
124
-
-
0030992874
-
An efficient asymmetric synthesis of (2S,3S)-3- trifluoromethylpyroglutamic acid
-
Soloshonok VA, Avilov DV, Kukhar VP, Meervelt LV, Mischenko N. An efficient asymmetric synthesis of (2S,3S)-3- trifluoromethylpyroglutamic acid. Tetrahedron Lett. 38, 4903-4904 (1997).
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 4903-4904
-
-
Soloshonok, V.A.1
Avilov, D.V.2
Kukhar, V.P.3
Meervelt, L.V.4
Mischenko, N.5
-
125
-
-
0033536721
-
Stereochemically defined c-substituted glutamic acids and their derivatives. 1. An efficient asymmetric synthesis of (2S,3S)-3-methyl- and -3-trifluoromethylpyroglutamic acids
-
Soloshonok VA, Cai C, Hruby VJ, Meervelt LV, Mischenko N. Stereochemically defined c-substituted glutamic acids and their derivatives. 1. An efficient asymmetric synthesis of (2S,3S)-3-methyl- and -3- trifluoromethylpyroglutamic acids. Tetrahedron 55, 12031-12044 (1999).
-
(1999)
Tetrahedron
, vol.55
, pp. 12031-12044
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
Meervelt, L.V.4
Mischenko, N.5
-
126
-
-
0033536604
-
Asymmetric synthesis of novel highly sterically constrained (2S,3S)-3-methyl-3- trifluoromethyl- and (2S,3S,4R)-3- trifluoromethyl-4- methylpyroglutamic acids
-
Soloshonok VA, Cai C, Hruby VJ, Meervelt LV. Asymmetric synthesis of novel highly sterically constrained (2S,3S)-3-methyl-3- trifluoromethyl- and (2S,3S,4R)-3- trifluoromethyl-4-methylpyroglutamic acids. Tetrahedron 55, 12045-12058 (1999).
-
(1999)
Tetrahedron
, vol.55
, pp. 12045-12058
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
Meervelt, L.V.4
-
127
-
-
0035936788
-
Michael addition reactions between chiral Ni(ii) complex of glycine and 3-(trans-enoyl) oxazolidin-2-ones. A case of electron donor- acceptor attractive interactions-controlled face diastereoselectivity
-
Cai C, Soloshonok VA, Hruby VJ. Michael addition reactions between chiral Ni(ii) complex of glycine and 3-(trans-enoyl) oxazolidin-2-ones. A case of electron donor- acceptor attractive interactions-controlled face diastereoselectivity. J. Org. Chem. 66, 1339-1350 (2001).
-
(2001)
J. Org. Chem.
, vol.66
, pp. 1339-1350
-
-
Cai, C.1
Soloshonok, V.A.2
Hruby, V.J.3
-
128
-
-
0034613131
-
Rational design of highly diastereoselective, organic base-catalyzed, room temperature michael addition reactions
-
Soloshonok VA, Cai C, Hruby VJ, Meervelt LV, Yamazaki T. Rational design of highly diastereoselective, organic base-catalyzed, room temperature michael addition reactions. J. Org. Chem. 65, 6688-6696 (2000).
-
(2000)
J. Org. Chem.
, vol.65
, pp. 6688-6696
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
Meervelt, L.V.4
Yamazaki, T.5
-
129
-
-
0033402142
-
Asymmetric michael addition reactions of chiral Ni(ii) complex of glycine with N-(enoyl)oxazolidinones: Improved reactivity and stereochemical outcome
-
Soloshonok VA, Cai C, Hruby VJ. Asymmetric michael addition reactions of chiral Ni(ii) complex of glycine with N-(enoyl)oxazolidinones: improved reactivity and stereochemical outcome. Tetrahedron: Asymmetry. 10, 4265-4269 (1999).
-
(1999)
Tetrahedron: Asymmetry.
, vol.10
, pp. 4265-4269
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
-
130
-
-
0034620199
-
Toward design of a practical methodology for stereocontrolled synthesis of χ-constrained pyroglutamic acids and related compounds. Virtually complete control of simple diastereoselectivity in the michael addition reactions of glycine ni(ii) complexes with N-(enoyl)oxazolidinones
-
Soloshonok VA, Cai C, Hruby VJ. Toward design of a practical methodology for stereocontrolled synthesis of χ-constrained pyroglutamic acids and related compounds. Virtually complete control of simple diastereoselectivity in the michael addition reactions of glycine ni(ii) complexes with N-(enoyl)oxazolidinones. Tetrahedron Lett. 41, 135-139 (2000).
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 135-139
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
-
131
-
-
0036942301
-
A convenient, room temperatureorganic base protocol for preparing chiral n-(enoyl)-1,3-oxazolidine-2-ones
-
Soloshonok VA, Ueki H, Jiang C, Cai C, Hruby VJ. A convenient, room temperatureorganic base protocol for preparing chiral n-(enoyl)-1,3-oxazolidine- 2-ones. Helv. Chim. Acta 85, 3616-3623 (2002).
-
(2002)
Helv. Chim. Acta
, vol.85
, pp. 3616-3623
-
-
Soloshonok, V.A.1
Ueki, H.2
Jiang, C.3
Cai, C.4
Hruby, V.J.5
-
132
-
-
0034674250
-
A practical asymmetric synthesis of enantiomerically pure 3-substituted pyroglutamic acids and related compounds
-
Soloshonok VA, Cai C, Hruby VJ. A practical asymmetric synthesis of enantiomerically pure 3-substituted pyroglutamic acids and related compounds. Angew. Chem. Int. Ed. Engl. 39, 2172-2175 (2000).
-
(2000)
Angew. Chem. Int. Ed. Engl.
, vol.39
, pp. 2172-2175
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
-
133
-
-
27544463710
-
Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(EEnoyl)- 4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of α-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity
-
Soloshonok VA, Cai C, Yamada T, Ueki H, Ohfune Y, Hruby VJ. Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(EEnoyl)- 4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of α-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity. J. Am. Chem. Soc. 127, 15296-15303 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15296-15303
-
-
Soloshonok, V.A.1
Cai, C.2
Yamada, T.3
Ueki, H.4
Ohfune, Y.5
Hruby, V.J.6
-
134
-
-
4344655353
-
Application of (S)- and (R)-methyl pyroglutamates as inexpensive, yet highly efficient chiral auxiliaries in the asymmetric michael addition reactions
-
Cai C, Yamada T, Tiwari R, Hruby VJ, Soloshonok VA. Application of (S)- and (R)-methyl pyroglutamates as inexpensive, yet highly efficient chiral auxiliaries in the asymmetric michael addition reactions. Tetrahedron Lett. 45, 6855-6858 (2004).
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 6855-6858
-
-
Cai, C.1
Yamada, T.2
Tiwari, R.3
Hruby, V.J.4
Soloshonok, V.A.5
-
135
-
-
0037911550
-
Efficient large-scale synthesis of picolinic acid derived Ni(II)-complexes of glycine
-
Ueki H, Ellis TK, Martin CH, Soloshonok VA. Efficient large-scale synthesis of picolinic acid derived Ni(II)-complexes of glycine. Eur. J. Org. Chem. 1954-1957 (2003).
-
(2003)
Eur. J. Org. Chem.
, pp. 1954-1957
-
-
Ueki, H.1
Ellis, T.K.2
Martin, C.H.3
Soloshonok, V.A.4
-
136
-
-
0034704633
-
(S) - Or (R)-N-(E-enoyl)-4-phenyl-1,3-oxazolidin-2- ones: Ideal michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives
-
Soloshonok VA, Cai C, Hruby VJ. (S)- or (R)-N-(E-enoyl)-4-phenyl-1,3- oxazolidin-2- ones: ideal michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivatives. Org. Letters 2, 747-750 (2000).
-
(2000)
Org. Letters
, vol.2
, pp. 747-750
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
-
137
-
-
0034598019
-
A unique case of face diastereoselectivity in the michael addition reactions between Ni(ii)-complexes of glycine and chiral 3-(E-enoyl)-1,3- oxazolidin- 2-ones
-
Soloshonok VA, Cai C, Hruby VJ. A unique case of face diastereoselectivity in the michael addition reactions between Ni(ii)-complexes of glycine and chiral 3-(E-enoyl)-1,3-oxazolidin- 2-ones. Tetrahedron Lett. 41, 9645-9649 (2000).
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 9645-9649
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
-
138
-
-
3543014960
-
Virtually complete control of simple and face diastereoselectivity in the michael addition reactions between achiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(Eenoyl)- 4-phenyl-1,3-oxazolidin-2-ones: Practical method for preparation of α-substituted pyroglutamic acids and pralines
-
Soloshonok VA, Ueki H, Tiwari R, Cai C, Hruby VJ. Virtually complete control of simple and face diastereoselectivity in the michael addition reactions between achiral equivalents of a nucleophilic glycine and (S)- or (R)-3-(Eenoyl)- 4-phenyl-1,3-oxazolidin-2-ones: practical method for preparation of α-substituted pyroglutamic acids and prolines. J. Org. Chem. 69, 4984-4990 (2004).
-
(2004)
J. Org. Chem.
, vol.69
, pp. 4984-4990
-
-
Soloshonok, V.A.1
Ueki, H.2
Tiwari, R.3
Cai, C.4
Hruby, V.J.5
-
139
-
-
12344332239
-
New generation of nucleophilic glycine equivalents
-
Soloshonok VA, Ueki H, Ellis TK. New generation of nucleophilic glycine equivalents. Tetrahedron Lett. 46, 941-944 (2005).
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 941-944
-
-
Soloshonok, V.A.1
Ueki, H.2
Ellis, T.K.3
-
140
-
-
12444311634
-
Application of modular nucleophilic glycine equivalents for truly practical asymmetric synthesis of α-substituted pyroglutamic acids
-
Soloshonok VA, Ueki H, Ellis TK, Yamada T, Ohfune Y. Application of modular nucleophilic glycine equivalents for truly practical asymmetric synthesis of α-substituted pyroglutamic acids. Tetrahedron Lett. 46, 1107-1110 (2005).
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 1107-1110
-
-
Soloshonok, V.A.1
Ueki, H.2
Ellis, T.K.3
Yamada, T.4
Ohfune, Y.5
-
141
-
-
33644991932
-
Design and synthesis of a new generation of 'NH' Ni(ii) complexes of glycine Schiff bases and their unprecedented C-H vs. N-H chemoselectivity in the alkyl halide alkylations and michael addition reactions
-
Soloshonok VA, Ellis TK. Design and synthesis of a new generation of 'NH' Ni(ii) complexes of glycine Schiff bases and their unprecedented C-H vs. N-H chemoselectivity in the alkyl halide alkylations and michael addition reactions. Synlett 533-538 (2006).
-
(2006)
Synlett
, pp. 533-538
-
-
Soloshonok, V.A.1
Ellis, T.K.2
-
142
-
-
67650555985
-
Resolution/deracemization of chiral α-amino acids using resolving reagents with flexible stereogenic centers
-
Soloshonok VA, Ellis TK, Ueki H, Ono T. Resolution/deracemization of chiral α-amino acids using resolving reagents with flexible stereogenic centers. J. Am. Chem. Soc. 131, 7208-7209 (2009).
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 7208-7209
-
-
Soloshonok, V.A.1
Ellis, T.K.2
Ueki, H.3
Ono, T.4
-
143
-
-
33750437425
-
The design, synthesis and evaluation of a new generation of modular nucleophilic glycine equivalents for the efficient synthesis of sterically constrained α-amino acids
-
Ellis TK, Ueki H, Yamada T, Ohfune Y, Soloshonok VA. The design, synthesis and evaluation of a new generation of modular nucleophilic glycine equivalents for the efficient synthesis of sterically constrained α-amino acids. J. Org. Chem. 71, 8572-8578 (2006).
-
(2006)
J. Org. Chem.
, vol.71
, pp. 8572-8578
-
-
Ellis, T.K.1
Ueki, H.2
Yamada, T.3
Ohfune, Y.4
Soloshonok, V.A.5
-
144
-
-
59349088064
-
Efficient asymmetric synthesis of the functionalized pyroglutamate core unit common to oxazolomycin and neooxazolomycin using michael reaction of nucleophilic glycine Schiff base with α,α-disubstituted acrylate
-
Yamada T, Sakaguchi K, Shinada T, Ohfune Y, Soloshonok VA. Efficient asymmetric synthesis of the functionalized pyroglutamate core unit common to oxazolomycin and neooxazolomycin using michael reaction of nucleophilic glycine Schiff base with α,α-disubstituted acrylate. Tetrahedron: Asymmetry 19, 2789-2795 (2008).
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 2789-2795
-
-
Yamada, T.1
Sakaguchi, K.2
Shinada, T.3
Ohfune, Y.4
Soloshonok, V.A.5
-
145
-
-
33845976663
-
Efficient asymmetric synthesis of novel 4-substituted and configurationally stable analogs of thalidomide
-
Yamada T, Okada T, Sakaguchi K, Ohfune Y, Ueki H, Soloshonok VA. Efficient asymmetric synthesis of novel 4-substituted and configurationally stable analogs of thalidomide. Org. Lett. 8, 5625-5628 (2006).
-
(2006)
Org. Lett.
, vol.8
, pp. 5625-5628
-
-
Yamada, T.1
Okada, T.2
Sakaguchi, K.3
Ohfune, Y.4
Ueki, H.5
Soloshonok, V.A.6
-
146
-
-
77953372156
-
-
Soloshonok VA, Yamada T, Sakaguchi K, Ohfune Y. Concise asymmetric synthesis of configurationally stable 4-trifluoromethyl thalidomide. 1(5), 897-908 (2009).
-
(2009)
Concise Asymmetric Synthesis of Configurationally Stable 4-trifluoromethyl Thalidomide
, vol.1
, Issue.5
, pp. 897-908
-
-
Soloshonok, V.A.1
Yamada, T.2
Sakaguchi, K.3
Ohfune, Y.4
-
147
-
-
33747663736
-
Use of chiral sulfoxides in asymmetric synthesis
-
Pellissier H. Use of chiral sulfoxides in asymmetric synthesis. Tetrahedron 62, 5559-5601 (2006).
-
(2006)
Tetrahedron
, vol.62
, pp. 5559-5601
-
-
Pellissier, H.1
-
148
-
-
4143050401
-
Recent advances in asymmetric reactions using sulfinimines (N-sulfinyl imines)
-
Zhou P, Chen BC, Davis F. Recent advances in asymmetric reactions using sulfinimines (N-sulfinyl imines). Tetrahedron 60, 8003-8030 (2004).
-
(2004)
Tetrahedron
, vol.60
, pp. 8003-8030
-
-
Zhou, P.1
Chen, B.C.2
Davis, F.3
-
149
-
-
33747113614
-
Chiral non-racemic sulfinimines. versatile reagents for asymmetric synthesis
-
Morton D, Stockman RA. Chiral non-racemic sulfinimines. versatile reagents for asymmetric synthesis. Tetrahedron 62, 8869-8905 (2006).
-
(2006)
Tetrahedron
, vol.62
, pp. 8869-8905
-
-
Morton, D.1
Stockman, R.A.2
-
150
-
-
12344252565
-
Analogues of key precursors of aspartyl protease inhibitors: Synthesis of trifluoromethyl amino epoxides
-
Ngoc Tam NT, Magueur G, Ourevitch M, Crousse B, Bégué JP, Bonnet-Delpon D. Analogues of key precursors of aspartyl protease inhibitors: synthesis of trifluoromethyl amino epoxides. J. Org. Chem. 70, 699-702 (2005).
-
(2005)
J. Org. Chem.
, vol.70
, pp. 699-702
-
-
Ngoc Tam, N.T.1
Magueur, G.2
Ourevitch, M.3
Crousse, B.4
Bégué, J.P.5
Bonnet-Delpon, D.6
-
151
-
-
29544437502
-
A concise asymmetric route for the synthesis of a novel class of glucocorticoid mimetics containing a trifluoromethyl-substituted alcohol
-
Lee TW, Proudfoot JR, Thomson DS. A concise asymmetric route for the synthesis of a novel class of glucocorticoid mimetics containing a trifluoromethyl-substituted alcohol. Bioorg. Med. Chem. Lett. 16, 654-657 (2006).
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 654-657
-
-
Lee, T.W.1
Proudfoot, J.R.2
Thomson, D.S.3
-
152
-
-
33846113396
-
Practical stereoselective synthesis of an α-trifluoromethyl- α-alkyl epoxide via a diastereoselective trifluoromethylation reaction
-
Song JJ, Tan Z, Xu J et al. Practical stereoselective synthesis of an α-trifluoromethyl-α-alkyl epoxide via a diastereoselective trifluoromethylation reaction. J. Org. Chem. 72, 292-294 (2007).
-
(2007)
J. Org. Chem.
, vol.72
, pp. 292-294
-
-
Song, J.J.1
Tan, Z.2
Xu, J.3
-
153
-
-
46749137489
-
Efficient synthesis of an α-trifluoromethyl-αtosyloxymethyl epoxide enabling stepwise double functionalisation to afford cf3- substituted tertiary alcohols
-
Keeling SP, Campbell IB, Coe DM et al. Efficient synthesis of an α-trifluoromethyl-αtosyloxymethyl epoxide enabling stepwise double functionalisation to afford cf3- substituted tertiary alcohols. Tetrahedron Lett. 49, 5101-5104 (2008).
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 5101-5104
-
-
Keeling, S.P.1
Campbell, I.B.2
Coe, D.M.3
-
154
-
-
58149339542
-
Improved ritter reaction with CF3-containing oxirane for an access to central units of protease inhibitors
-
Dos Santos M, Crousse B, Bonnet-Delpon D. Improved ritter reaction with CF3-containing oxirane for an access to central units of protease inhibitors. Tetrahedron Lett. 50, 857-859 (2009).
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 857-859
-
-
Dos Santos, M.1
Crousse, B.2
Bonnet-Delpon, D.3
-
155
-
-
0006016547
-
Stereoselective oxirane formation by reaction of diazomethane on 1-fluoro-3-[(4- methylphenyl)sulfinyl]-3-phenylpropan-2- one
-
Bravo P, Frigerio M, Fronza G et al. Stereoselective oxirane formation by reaction of diazomethane on 1-fluoro-3-[(4- methylphenyl)sulfinyl]-3- phenylpropan-2- one. Can. J. Chem. 72, 1769-1779 (1994).
-
(1994)
Can. J. Chem.
, vol.72
, pp. 1769-1779
-
-
Bravo, P.1
Frigerio, M.2
Fronza, G.3
-
156
-
-
0007374181
-
Reactions of α-substituted α-keto-α-fluoro sulfoxides
-
Arnone A, Bravo P, Frigerio M et al. Reactions of α-substituted α-keto-α-fluoro sulfoxides with diazomethane. A general approach to enantiomerically pure α-fluoromethyl-α′,α′- alkyl/alkenyl-sulfinylmethyl oxiranes. Gazz. Chim. Ital. 127, 819-826 (1997).
-
(1997)
Gazz. Chim. Ital.
, vol.127
, pp. 819-826
-
-
Arnone, A.1
Bravo, P.2
Frigerio, M.3
-
157
-
-
0032563998
-
Synthesis and reactivity of enantiomerically pure 2-fluoromethyl-2- (1́-ptolylsulfinyl) alkyl oxiranes
-
Arnone A, Bravo P, Frigerio M, Viani F, Soloshonok VA. Synthesis and reactivity of enantiomerically pure 2-fluoromethyl-2-(1́-ptolylsulfinyl) alkyl oxiranes. Tetrahedron 54, 11825-11840 (1998).
-
(1998)
Tetrahedron
, vol.54
, pp. 11825-11840
-
-
Arnone, A.1
Bravo, P.2
Frigerio, M.3
Viani, F.4
Soloshonok, V.A.5
-
158
-
-
0032564004
-
Highly diastereoselective methylene transfer from diazomethane to the carbonyl of α-keto sulfoxides. A general approach to synthetically versatile fluorinecontaining chiral building blocks
-
Arnone A, Bravo P, Frigerio M, Viani F, Soloshonok VA. Highly diastereoselective methylene transfer from diazomethane to the carbonyl of α-keto sulfoxides. A general approach to synthetically versatile fluorinecontaining chiral building blocks. Tetrahedron 54, 11841-11860 (1998).
-
(1998)
Tetrahedron
, vol.54
, pp. 11841-11860
-
-
Arnone, A.1
Bravo, P.2
Frigerio, M.3
Viani, F.4
Soloshonok, V.A.5
-
159
-
-
33646846110
-
Trifluoromethylated amino alcohol as chiral auxiliary for highly diastereoselective and fast simmons-smith cyclopropanation of allylic amine
-
Katagiri T, Iguchi N, Kawate T, Takahashi S, Uneyama K. Trifluoromethylated amino alcohol as chiral auxiliary for highly diastereoselective and fast simmons-smith cyclopropanation of allylic amine. Tetrahedron: Asymmetry 17, 1157-1160 (2006).
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 1157-1160
-
-
Katagiri, T.1
Iguchi, N.2
Kawate, T.3
Takahashi, S.4
Uneyama, K.5
-
160
-
-
44649155005
-
Improvement of the asymmetry-inducing ability of a trifluoromethylated amino alcohol by electron donation to a CF3 group
-
Harada A, Fujiwara Y, Katagiri T. Improvement of the asymmetry-inducing ability of a trifluoromethylated amino alcohol by electron donation to a CF3 group. Tetrahedron: Asymmetry 19, 1210-1214 (2008).
-
(2008)
Tetrahedron: Asymmetry
, vol.19
, pp. 1210-1214
-
-
Harada, A.1
Fujiwara, Y.2
Katagiri, T.3
-
161
-
-
45449109768
-
Synthesis and utilization of trifluoromethylated amino alcohol ligands for the enantioselective reformatsky reaction and addition of diethylzinc to n-(diphenylphosphinoyl)imine
-
Xu X-H, Qiu X-L, Qing F-L. Synthesis and utilization of trifluoromethylated amino alcohol ligands for the enantioselective reformatsky reaction and addition of diethylzinc to n-(diphenylphosphinoyl)imine. Tetrahedron 64, 7353-7361 (2008).
-
(2008)
Tetrahedron
, vol.64
, pp. 7353-7361
-
-
Xu, X.-H.1
Qiu, X.-L.2
Qing, F.-L.3
-
162
-
-
0027426848
-
Optically pure and fluoro substituted carboacyclic nucleoside analogues
-
Bravo P, Frigerio M, Soloshonok V, Viani F. Optically pure and fluoro substituted carboacyclic nucleoside analogues. Tetrahedron Lett. 34, 7771-7772 (1993).
-
(1993)
Tetrahedron Lett
, vol.34
, pp. 7771-7772
-
-
Bravo, P.1
Frigerio, M.2
Soloshonok, V.3
Viani, F.4
-
163
-
-
0028362360
-
New fluorinated chiral synthons
-
Bravo P, Farina A, Frigerio M, Valdo Meille S, Viani F, Soloshonok V. New fluorinated chiral synthons. Tetrahedron: Asymmetry 5, 987-1004 (1994).
-
(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 987-1004
-
-
Bravo, P.1
Farina, A.2
Frigerio, M.3
Valdo Meille, S.4
Viani, F.5
Soloshonok, V.6
-
164
-
-
0028051675
-
Synthesis of optically pure (R)- and (S)-α-trifluoromethylalanine
-
Bravo P, Capelli S, Meille SV et al. Synthesis of optically pure (R)- and (S)-α-trifluoromethylalanine. Tetrahedron: Asymmetry 5, 2009-2018 (1994).
-
(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 2009-2018
-
-
Bravo, P.1
Capelli, S.2
Meille, S.V.3
-
165
-
-
0002167469
-
Synthesis of enantiomerically pure (R)- and (S)-α- trifluoromethylserine
-
Bravo P, Viani F, Zanda M, Soloshonok V. Synthesis of enantiomerically pure (R)- and (S)-α-trifluoromethylserine. Gazz. Chim. Ital. 125, 149-150 (1995).
-
(1995)
Gazz. Chim. Ital.
, vol.125
, pp. 149-150
-
-
Bravo, P.1
Viani, F.2
Zanda, M.3
Soloshonok, V.4
-
166
-
-
0000011350
-
Synthesis of both enantiomers of α-(trifluoromethyl) butyrine and α-(trifluoromethyl) phenylalanine
-
Bravo P, Viani F, Zanda M et al. Synthesis of both enantiomers of α-(trifluoromethyl) butyrine and α-(trifluoromethyl) phenylalanine. Gazz. Chim. Ital. 126, 645-652 (1996).
-
(1996)
Gazz. Chim. Ital.
, vol.126
, pp. 645-652
-
-
Bravo, P.1
Viani, F.2
Zanda, M.3
-
167
-
-
8544244902
-
Stereoselective additions of α-lithiated alkyl-p-tolylsulfoxides to N-PMP (fluoroalkyl) aldimines. An efficient approach to enantiomerically pure fluoro amino compounds
-
Bravo P, Farina A, Kukhar VP et al. Stereoselective additions of α-lithiated alkyl-p-tolylsulfoxides to N-PMP (fluoroalkyl) aldimines. An efficient approach to enantiomerically pure fluoro amino compounds. J. Org. Chem. 62, 3424-3425 (1997).
-
(1997)
J. Org. Chem.
, vol.62
, pp. 3424-3425
-
-
Bravo, P.1
Farina, A.2
Kukhar, V.P.3
-
168
-
-
0032532260
-
Chiral sulfoxide controlled asymmetric additions to c-n double bond. An efficient approach to stereochemically defined α-fluoroalkyl amino compounds
-
Bravo P, Guidetti M, Viani F et al. Chiral sulfoxide controlled asymmetric additions to c-n double bond. An efficient approach to stereochemically defined α-fluoroalkyl amino compounds. Tetrahedron 54, 12789-12806 (1998).
-
(1998)
Tetrahedron
, vol.54
, pp. 12789-12806
-
-
Bravo, P.1
Guidetti, M.2
Viani, F.3
-
169
-
-
0033525459
-
Asymmetric synthesis of α-arylglycinols via additions of lithium methyl p-tolyl sulfoxide to n-(pmp)arylaldimines followed by 'non oxidative' pummerer reaction
-
Bravo P, Capelli S, Crucianelli M et al. Asymmetric synthesis of α-arylglycinols via additions of lithium methyl p-tolyl sulfoxide to n-(pmp)arylaldimines followed by 'non oxidative' pummerer reaction. Tetrahedron 55, 3025-3040 (1999).
-
(1999)
Tetrahedron
, vol.55
, pp. 3025-3040
-
-
Bravo, P.1
Capelli, S.2
Crucianelli, M.3
-
170
-
-
0002877308
-
Synthesis and biochemical applications of fluorine-containing peptides and proteins
-
Kukhar VP, Soloshonok VA (Eds). John Wiley & Sons, Chichester, UK
-
Kirk KL. Synthesis and biochemical applications of fluorine-containing peptides and proteins. In: Fluorine-containing Amino Acids. Kukhar VP, Soloshonok VA (Eds). John Wiley & Sons, Chichester, UK (1995).
-
(1995)
Fluorine-containing Amino Acids
-
-
Kirk, K.L.1
-
171
-
-
0034611513
-
Synthesis and antifungal activity of rhodopeptin analogues. 2. Modification of the west amino acid moiety
-
Nakayama K, Kawato H, Inagaki H et al. Synthesis and antifungal activity of rhodopeptin analogues. 2. Modification of the west amino acid moiety. Org. Lett. 2, 977-980 (2000).
-
(2000)
Org. Lett.
, vol.2
, pp. 977-980
-
-
Nakayama, K.1
Kawato, H.2
Inagaki, H.3
-
172
-
-
0037111684
-
Asymmetric synthesis of α,α-difluoro-Βamino acid derivatives from enantiomerically pure n-tert-butylsulfinimines
-
Staas D, Savage K, Homnick C, Tsou N, Ball R. Asymmetric synthesis of α,α-difluoro-Βamino acid derivatives from enantiomerically pure n-tert-butylsulfinimines. J. Org. Chem. 67, 8276-8279 (2002).
-
(2002)
J. Org. Chem.
, vol.67
, pp. 8276-8279
-
-
Staas, D.1
Savage, K.2
Homnick, C.3
Tsou, N.4
Ball, R.5
-
173
-
-
33644766802
-
Unequivocal synthesis of (Z)-alkene and (E)-fluoroalkene dipeptide isosteres to probe structural requirements of the peptide transporter PEPT1
-
Niida A, Tomita K, Mizumoto M et al. Unequivocal synthesis of (Z)-alkene and (E)-fluoroalkene dipeptide isosteres to probe structural requirements of the peptide transporter PEPT1. Org. Lett. 8, 613-616 (2006).
-
(2006)
Org. Lett.
, vol.8
, pp. 613-616
-
-
Niida, A.1
Tomita, K.2
Mizumoto, M.3
-
174
-
-
41549104832
-
Diastereoselective synthesis of highly functionalized fluoroalkene dipeptide isosteres and its application to fmoc-based solid-phase synthesis of a cyclic pentapeptide mimetic
-
Narumi T, Tomita K, Inokuchi E et al. Diastereoselective synthesis of highly functionalized fluoroalkene dipeptide isosteres and its application to fmoc-based solid-phase synthesis of a cyclic pentapeptide mimetic. Tetrahedron 64, 4332-4346 (2008).
-
(2008)
Tetrahedron
, vol.64
, pp. 4332-4346
-
-
Narumi, T.1
Tomita, K.2
Inokuchi, E.3
-
175
-
-
0031390567
-
Synthesis and structure-activity relationships of novel 2́,2́-difluoro analogs of docetaxel
-
Uoto K, Ohsuki S, Takenoshita H et al. Synthesis and structure-activity relationships of novel 2́,2́-difluoro analogs of docetaxel. Chem. Pharm. Bull. 45, 1793 - 1804 (1997).
-
(1997)
Chem. Pharm. Bull.
, vol.45
, pp. 1793-1804
-
-
Uoto, K.1
Ohsuki, S.2
Takenoshita, H.3
-
176
-
-
43049159434
-
Rhodium-catalyzed reformatsky-type reaction for asymmetric synthesis of difluoro-Β-lactams using menthyl group as a chiral auxiliary
-
Tarui A, Ozaki D, Nakajima N et al. Rhodium-catalyzed reformatsky-type reaction for asymmetric synthesis of difluoro-Β-lactams using menthyl group as a chiral auxiliary. Tetrahedron Lett. 49, 3839-3843 (2008).
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 3839-3843
-
-
Tarui, A.1
Ozaki, D.2
Nakajima, N.3
-
177
-
-
35548949301
-
Chemoselective and stereoselective synthesis of gem-difluoro- Βaminoesters or gem-difluoro-Β-lactams from ethylbromodifluoroacetate and imines during reformatsky reaction
-
Boyer N, Gloanec P, De Nanteuil G, Jubaulta P, Quiriona JC. Chemoselective and stereoselective synthesis of gem-difluoro-Βaminoesters or gem-difluoro-Β-lactams from ethylbromodifluoroacetate and imines during reformatsky reaction. Tetrahedron 63, 12352-12366 (2007).
-
(2007)
Tetrahedron
, vol.63
, pp. 12352-12366
-
-
Boyer, N.1
Gloanec, P.2
De Nanteuil, G.3
Jubaulta, P.4
Quiriona, J.C.5
-
178
-
-
1442324529
-
2-mediated reduction of γ,γ-difluoro-α, Βenoates with application to the synthesis of functionalized (z)-fluoroalkene-type dipeptide isosteres
-
2-mediated reduction of γ,γ-difluoro-α,Βenoates with application to the synthesis of functionalized (z)-fluoroalkene-type dipeptide isosteres. J. Org. Chem. 69, 1634-1645 (2004).
-
(2004)
J. Org. Chem.
, vol.69
, pp. 1634-1645
-
-
Otaka, A.1
Watanabe, J.2
Yukimasa, A.3
-
179
-
-
4544347622
-
The reformatsky reaction in organic synthesis. Recent advances
-
Ocampoa R, Dolbier WR. The reformatsky reaction in organic synthesis. Recent advances. Tetrahedron 60, 9325-9374 (2004).
-
(2004)
Tetrahedron
, vol.60
, pp. 9325-9374
-
-
Ocampoa, R.1
Dolbier, W.R.2
-
180
-
-
0034847357
-
The mitsunobu reaction in the synthesis of α,α-difluoro- Β-amino acids
-
Fokina NA, Kornilov AM, Kukhar VP. The mitsunobu reaction in the synthesis of α,α-difluoro-Β-amino acids. J. Fluorine Chem. 111, 69-76 (2001).
-
(2001)
J. Fluorine Chem.
, vol.111
, pp. 69-76
-
-
Fokina, N.A.1
Kornilov, A.M.2
Kukhar, V.P.3
-
181
-
-
0037194175
-
Convenient, large-scale asymmetric synthesis of Β-aryl-substituted α,α-difluoroΒ- amino acids
-
Soloshonok VA, Ohkura H, Sorochinsky A et al. Convenient, large-scale asymmetric synthesis of Β-aryl-substituted α,α-difluoroΒ- amino acids. Tetrahedron Lett. 43, 5445-5448 (2002).
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 5445-5448
-
-
Soloshonok, V.A.1
Ohkura, H.2
Sorochinsky, A.3
-
182
-
-
0141454899
-
Convenient asymmetric synthesis of Β-substituted α,α-difluoro-α-amino acids via reformatsky reaction between davis' n-sulfinylimines and ethyl bromodifluoroacetate
-
Sorochinsky A, Voloshin N, Markovsky A et al. Convenient asymmetric synthesis of Β-substituted α,α-difluoro-α-amino acids via reformatsky reaction between davis' n-sulfinylimines and ethyl bromodifluoroacetate. J. Org. Chem. 68, 7448-7454 (2003).
-
(2003)
J. Org. Chem.
, vol.68
, pp. 7448-7454
-
-
Sorochinsky, A.1
Voloshin, N.2
Markovsky, A.3
-
183
-
-
0002958143
-
The biological activity of phosphono- and phosphinopeptides
-
Kukhar VP, Hudson HR (Eds). John Wiley and Sons, Chichester, UK
-
Kafarski P, Lejczak B. The biological activity of phosphono- and phosphinopeptides. In: Aminophosphonic and Aminophosphinic Acids. Chemistry and Biological Activity. Kukhar VP, Hudson HR (Eds). John Wiley and Sons, Chichester, UK, 407-442 (2000).
-
(2000)
Aminophosphonic and Aminophosphinic Acids. Chemistry and Biological Activity
, pp. 407-442
-
-
Kafarski, P.1
Lejczak, B.2
-
184
-
-
33749857513
-
Fluorinated phosphonates: Synthesis and biomedical application
-
Romanenko VD, Kukhar VP. Fluorinated phosphonates: synthesis and biomedical application. Chem. Rev. 106, 3868-3935 (2006).
-
(2006)
Chem. Rev.
, vol.106
, pp. 3868-3935
-
-
Romanenko, V.D.1
Kukhar, V.P.2
-
185
-
-
17944382648
-
Acyclic and cyclic aminophosphonic acids: Asymmetric syntheses mediated by chiral sulfinyl auxiliary
-
Mikolajczyk M. Acyclic and cyclic aminophosphonic acids: asymmetric syntheses mediated by chiral sulfinyl auxiliary. J. Organometall. Chem. 690, 2488-2496 (2005).
-
(2005)
J. Organometall. Chem.
, vol.690
, pp. 2488-2496
-
-
Mikolajczyk, M.1
-
186
-
-
56949101063
-
An overview of stereoselective synthesis of α-aminophosphonic acids and derivatives
-
Ordonez M, Rojas-Cabrera H, Cativiela C. An overview of stereoselective synthesis of α-aminophosphonic acids and derivatives. Tetrahedron 65, 17-49 (2009).
-
(2009)
Tetrahedron
, vol.65
, pp. 17-49
-
-
Ordonez, M.1
Rojas-Cabrera, H.2
Cativiela, C.3
-
187
-
-
77953401126
-
-
Röschenthaler GV, Kukhar V, Barten J, Gvozdovska N, Belik M, Sorochinsky A. Asymmetric synthesis of α, α-difluoro-Β
-
Röschenthaler GV, Kukhar V, Barten J, Gvozdovska N, Belik M, Sorochinsky A. Asymmetric synthesis of α, α-difluoro-Β
-
-
-
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