-
1
-
-
0029936364
-
Z-2-phenyl-4-[(S)-2,2-dimethyl-1,3-dioxolan-4-ylmethylen]-5(4H)-oxazolone as the dienophile in asymmetric Diels-Alder reactions
-
10.1016/0957-4166(96)00160-7 1:CAS:528:DyaK28XjsVCgtLk%3D
-
Bunuel E, Cativiela C, de Diaz Villegas MD (1996a) Z-2-phenyl-4-[(S)-2,2- dimethyl-1,3-dioxolan-4-ylmethylen]-5(4H)-oxazolone as the dienophile in asymmetric Diels-Alder reactions. Tetrahedron: Asymm 7:1431-1436
-
(1996)
Tetrahedron: Asymm
, vol.7
, pp. 1431-1436
-
-
Bunuel, E.1
Cativiela, C.2
De Diaz Villegas, M.D.3
-
2
-
-
0029890686
-
Diastereoselective synthesis of (1S,2S,3R,4R)- and (1R,2S,3R,4S)- bicyclo[2.2.1]hept-2-amino-2,3-dicarboxylic acids: New conformationally- constrained (S)-aspartic acid analogues
-
10.1016/0957-4166(96)00172-3 1:CAS:528:DyaK28XjsVCgtbc%3D
-
Bunuel E, Cativiela C, de Diaz Villegas MD (1996b) Diastereoselective synthesis of (1S,2S,3R,4R)- and (1R,2S,3R,4S)-bicyclo[2.2.1]hept-2-amino-2,3- dicarboxylic acids: new conformationally-constrained (S)-aspartic acid analogues. Tetrahedron: Asymm 7:1521-1528
-
(1996)
Tetrahedron: Asymm
, vol.7
, pp. 1521-1528
-
-
Bunuel, E.1
Cativiela, C.2
De Diaz Villegas, M.D.3
-
3
-
-
49249107343
-
Stereoselective synthesis of 3,4,5,6-tetrahydroxycyclohexyl β-amino acid derivatives
-
10.1016/j.tetlet.2008.07.094 1:CAS:528:DC%2BD1cXhtVWks7fN
-
Chola J, Masesane IB (2008) Stereoselective synthesis of 3,4,5,6-tetrahydroxycyclohexyl β-amino acid derivatives. Tetrahedron Lett 49:5680-5682
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 5680-5682
-
-
Chola, J.1
Masesane, I.B.2
-
4
-
-
47749126264
-
Chemistry of norbornane/ene and heteronorbornane/ene β-amino acids
-
10.2174/157017908784221576 1:CAS:528:DC%2BD1cXot1OmsrY%3D
-
Csende F, Fulop F, Stajer G (2008) Chemistry of norbornane/ene and heteronorbornane/ene β-amino acids. Curr Org Syn 5:173-185
-
(2008)
Curr Org Syn
, vol.5
, pp. 173-185
-
-
Csende, F.1
Fulop, F.2
Stajer, G.3
-
5
-
-
35948949763
-
One-pot, large-scale synthesis of Nickel(II) complexes derived from 2-[N-(α-picolyl)amino]benzophenone (PABP) and α- Or β-amino acids
-
17949038 10.1021/jo071011e 1:CAS:528:DC%2BD2sXhtFyhu73P
-
Deng G, Wang J, Zhou Y, Jiang H, Liu H (2007) One-pot, large-scale synthesis of Nickel(II) complexes derived from 2-[N-(α-picolyl)amino] benzophenone (PABP) and α- or β-amino acids. J Org Chem 72:8932-8934
-
(2007)
J Org Chem
, vol.72
, pp. 8932-8934
-
-
Deng, G.1
Wang, J.2
Zhou, Y.3
Jiang, H.4
Liu, H.5
-
6
-
-
84962105974
-
Synthesen in der hydroaromatischen Reihe
-
10.1002/jlac.19284600106 1:CAS:528:DyaB1cXpsFyn
-
Diels O, Alder K (1928) Synthesen in der hydroaromatischen Reihe. Just Lieb Ann Chem 460:98-122
-
(1928)
Just Lieb Ann Chem
, vol.460
, pp. 98-122
-
-
Diels, O.1
Alder, K.2
-
7
-
-
68049085769
-
Efficient synthesis of α-aryl-/heteroaryl-substituted β-amino acids via Ni(II) complex through the Suzuki coupling reaction
-
19719254 10.1021/jo900469d 1:CAS:528:DC%2BD1MXntVSkt7s%3D
-
Ding X, Ye D, Liu F, Deng G, Liu G, Luo X, Jiang H, Liu H (2009) Efficient synthesis of α-aryl-/heteroaryl-substituted β-amino acids via Ni(II) complex through the Suzuki coupling reaction. J Org Chem 74:5656-5659
-
(2009)
J Org Chem
, vol.74
, pp. 5656-5659
-
-
Ding, X.1
Ye, D.2
Liu, F.3
Deng, G.4
Liu, G.5
Luo, X.6
Jiang, H.7
Liu, H.8
-
8
-
-
0038277395
-
Efficient synthesis of 2-aminoindane-2-carboxylic acid via dialkylation of nucleophilic glycine equivalent
-
12790614 10.1021/jo030065v 1:CAS:528:DC%2BD3sXjs1Gntr8%3D
-
Ellis TK, Hochla VM, Soloshonok VA (2003a) Efficient synthesis of 2-aminoindane-2-carboxylic acid via dialkylation of nucleophilic glycine equivalent. J Org Chem 68:4973-4976
-
(2003)
J Org Chem
, vol.68
, pp. 4973-4976
-
-
Ellis, T.K.1
Hochla, V.M.2
Soloshonok, V.A.3
-
9
-
-
0043032849
-
Efficient synthesis of sterically constrained symmetrically α, α-disubstituted α-amino acids under operationally convenient conditions
-
12895052 10.1021/jo030075w 1:CAS:528:DC%2BD3sXltF2ku7w%3D
-
Ellis TK, Martin CH, Tsai GM, Ueki H, Soloshonok VA (2003b) Efficient synthesis of sterically constrained symmetrically α, α-disubstituted α-amino acids under operationally convenient conditions. J Org Chem 68:6208-6214
-
(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
-
10
-
-
12344332239
-
New generation of nucleophilic glycine equivalents
-
10.1016/j.tetlet.2004.12.050 1:CAS:528:DC%2BD2MXksVehsw%3D%3D
-
Ellis TK, Ueki H, Soloshonok VA (2005) New generation of nucleophilic glycine equivalents. Tetrahedron Lett 46:941-944
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 941-944
-
-
Ellis, T.K.1
Ueki, H.2
Soloshonok, V.A.3
-
11
-
-
33750437425
-
Design, synthesis, and evaluation of a new generation of modular nucleophilic glycine equivalents for the efficient synthesis of sterically constrained α-amino acids
-
17064036 10.1021/jo0616198 1:CAS:528:DC%2BD28XhtVaku7%2FF
-
Ellis TK, Ueki H, Yamada T, Ohfune Y, Soloshonok VA (2006) 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)
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
-
12
-
-
3242701305
-
Antimicrobial 14-helical β-peptides: Potent bilayer disrupting agents
-
15260496 10.1021/bi049414l 1:CAS:528:DC%2BD2cXltl2lurs%3D
-
Epand RF, Raguse TL, Gellman SH, Epand RM (2004) Antimicrobial 14-helical β-peptides: potent bilayer disrupting agents. Biochemistry 43:9527-9535
-
(2004)
Biochemistry
, vol.43
, pp. 9527-9535
-
-
Epand, R.F.1
Raguse, T.L.2
Gellman, S.H.3
Epand, R.M.4
-
13
-
-
0000847908
-
Asymmetric Diels-Alder reaction. A facile route to chiral alkyl hydrogen cyclohexene-1,2-dicarboxylate
-
10.1016/S0040-4039(01)81069-8 1:CAS:528:DyaL1cXlsVyqsLw%3D
-
Furuta K, Hayashi S, Miwa Y, Yamamoto H (1987) Asymmetric Diels-Alder reaction. A facile route to chiral alkyl hydrogen cyclohexene-1,2-dicarboxylate. Tetrahedron Lett 28:5841-5844
-
(1987)
Tetrahedron Lett
, vol.28
, pp. 5841-5844
-
-
Furuta, K.1
Hayashi, S.2
Miwa, Y.3
Yamamoto, H.4
-
14
-
-
0842329029
-
Two helical conformations from a single foldamer backbone: "split personality" in short α/β-peptides
-
10.1002/anie.200352125 1:CAS:528:DC%2BD2cXhtVWksro%3D
-
Hayen A, Schmitt MA, Ngassa FN, Thomasson KA, Gellmann SH (2004) Two helical conformations from a single foldamer backbone: "split personality" in short α/β-peptides. Angew Chem Int Ed 43:505-510
-
(2004)
Angew Chem Int Ed
, vol.43
, pp. 505-510
-
-
Hayen, A.1
Schmitt, M.A.2
Ngassa, F.N.3
Thomasson, K.A.4
Gellmann, S.H.5
-
15
-
-
0025019332
-
FR109615, a new antifungal antibiotic from Streptomyces setonii. Taxonomy, fermentation, isolation, physico-chemical properties and biological activity
-
10.7164/antibiotics.43.1 1:CAS:528:DyaK3cXhsFWgsr8%3D
-
Iwamoto T, Tsujii E, Ezaki M, Fujie A, Hashimoto S, Okuhara M, Kohsaka M, Imanaka H, Kawabata K, Inamoto Y, Sakane K (1990) FR109615, a new antifungal antibiotic from Streptomyces setonii. Taxonomy, fermentation, isolation, physico-chemical properties and biological activity. J Antibiotics 43:1-7
-
(1990)
J Antibiotics
, vol.43
, pp. 1-7
-
-
Iwamoto, T.1
Tsujii, E.2
Ezaki, M.3
Fujie, A.4
Hashimoto, S.5
Okuhara, M.6
Kohsaka, M.7
Imanaka, H.8
Kawabata, K.9
Inamoto, Y.10
Sakane, K.11
-
17
-
-
0024835032
-
Cispentacin, a new antifungal antibiotic. II. in vitro and in vivo antifungal activities
-
10.7164/antibiotics.42.1756 1:CAS:528:DyaK3cXpsFentg%3D%3D
-
Oki T, Hirano M, Tomatsu K, Numata K, Kamei H (1989) Cispentacin, a new antifungal antibiotic. II. In vitro and in vivo antifungal activities. J Antibiotics 42:1756-1762
-
(1989)
J Antibiotics
, vol.42
, pp. 1756-1762
-
-
Oki, T.1
Hirano, M.2
Tomatsu, K.3
Numata, K.4
Kamei, H.5
-
18
-
-
0040368144
-
Octaline and decalone derivatives from a new annulation reaction in enamine field
-
10.1016/0040-4020(77)80463-8 1:CAS:528:DyaE1cXhs12lt70%3D
-
Pitacco G, Risaliti A, Trevisan ML, Valentin E (1977) Octaline and decalone derivatives from a new annulation reaction in enamine field. Tetrahedron 33:3145-3148
-
(1977)
Tetrahedron
, vol.33
, pp. 3145-3148
-
-
Pitacco, G.1
Risaliti, A.2
Trevisan, M.L.3
Valentin, E.4
-
19
-
-
0034697001
-
Convenient, large-scale asymmetric synthesis of enantiomerically pure trans-cinnamylglycine and -α-alanine
-
10.1016/S0040-4020(00)00176-9 1:CAS:528:DC%2BD3cXjtVemtLo%3D
-
Qiu W, Soloshonok VA, Cai C, Tang X, Hruby VJ (2000) Convenient, large-scale asymmetric synthesis of enantiomerically pure trans-cinnamylglycine and -α-alanine. Tetrahedron 56:2577-2582
-
(2000)
Tetrahedron
, vol.56
, pp. 2577-2582
-
-
Qiu, W.1
Soloshonok, V.A.2
Cai, C.3
Tang, X.4
Hruby, V.J.5
-
20
-
-
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
-
10.2174/1385272024605014 1:CAS:528:DC%2BD38Xmslyiurc%3D
-
Soloshonok VA (2002) 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)
Curr Org Chem
, vol.6
, pp. 341-364
-
-
Soloshonok, V.A.1
-
21
-
-
37049079441
-
Asymmetric synthesis of phosphorus analogues of dicarboxylic α-amino acids
-
10.1039/p19920001525
-
Soloshonok VA, Belokon YN, Kuzmina NA, Maleev VI, Svistunova NY, Solodenko VA, Kukhar VP (1992) Asymmetric synthesis of phosphorus analogues of dicarboxylic α-amino acids. J Chem Soc Perkin Trans I 1992:1525-1529
-
(1992)
J Chem Soc Perkin Trans i
, vol.1992
, pp. 1525-1529
-
-
Soloshonok, V.A.1
Belokon, Y.N.2
Kuzmina, N.A.3
Maleev, V.I.4
Svistunova, N.Y.5
Solodenko, V.A.6
Kukhar, V.P.7
-
22
-
-
0029163546
-
Asymmetric aldol reactions of chiral Ni(II)-complex of glycine with aliphatic aldehydes. Stereodivergent synthesis of syn-(2S)- and syn-(2R)-β-alkylserines
-
10.1016/0957-4166(95)00220-J 1:CAS:528:DyaK2MXnvVCmtrk%3D
-
Soloshonok VA, Avilov DV, Kukhar VP, Tararov VI, Saveleva TF, Churkina TD, Ikonnikov NS, Kochetkov KA, Orlova SA, Pysarevsky AP, Struchkov YT, Raevsky NI, Belokon YN (1995) Asymmetric aldol reactions of chiral Ni(II)-complex of glycine with aliphatic aldehydes. Stereodivergent synthesis of syn-(2S)- and syn-(2R)-β-alkylserines. Tetrahedron: Asymm 6:1741-1756
-
(1995)
Tetrahedron: Asymm
, vol.6
, pp. 1741-1756
-
-
Soloshonok, V.A.1
Avilov, D.V.2
Kukhar, V.P.3
Tararov, V.I.4
Saveleva, T.F.5
Churkina, T.D.6
Ikonnikov, N.S.7
Kochetkov, K.A.8
Orlova, S.A.9
Pysarevsky, A.P.10
Struchkov, Y.T.11
Raevsky, N.I.12
Belokon, Y.N.13
-
23
-
-
0029883406
-
Highly diastereoselective asymmetric aldol reactions of chiral Ni(II)-complex of glycine with alkyl trifluoromethyl ketones
-
10.1016/0957-4166(96)00177-2 1:CAS:528:DyaK28XjvVKnsLY%3D
-
Soloshonok VA, Avilov DV, Kukhar VP (1996a) Highly diastereoselective asymmetric aldol reactions of chiral Ni(II)-complex of glycine with alkyl trifluoromethyl ketones. Tetrahedron: Asymm 7:1547-1550
-
(1996)
Tetrahedron: Asymm
, vol.7
, pp. 1547-1550
-
-
Soloshonok, V.A.1
Avilov, D.V.2
Kukhar, V.P.3
-
24
-
-
0030590464
-
Asymmetric aldol reactions of trifluoromethyl ketones with a chiral Ni(II) complex of glycine: Stereocontrolling effect of the trifluoromethyl group
-
10.1016/0040-4020(96)00741-7 1:CAS:528:DyaK28XlvV2mt78%3D
-
Soloshonok VA, Avilov DV, Kukhar VP (1996b) 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)
Tetrahedron
, vol.52
, pp. 12433-12442
-
-
Soloshonok, V.A.1
Avilov, D.V.2
Kukhar, V.P.3
-
25
-
-
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
-
10.1016/S0040-4039(97)00963-5 1:CAS:528:DyaK2sXktlejurg%3D
-
Soloshonok VA, Avilov DV, Kukhar VP, Meervelt LV, Mischenko N (1997) 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)
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
-
26
-
-
0033536721
-
Stereochemically defined C-substituted glutamic acids and their derivatives. 1. An efficient asymmetric synthesis of (2S,3S)-3-methyl- and -3-trifluoromethylpyroglutamic acids
-
10.1016/S0040-4020(99)00711-5 1:CAS:528:DyaK1MXmsVOqtr8%3D
-
Soloshonok VA, Cai C, Hruby VJ, Meervelt LV, Mischenko N (1999a) 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)
Tetrahedron
, vol.55
, pp. 12031-12044
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
Meervelt, L.V.4
Mischenko, N.5
-
27
-
-
0033536604
-
Asymmetric synthesis of novel highly sterically constrained (2S,3S)-3-methyl-3-trifluoromethyl- and (2S,3S,4R)-3-trifluoromethyl-4- methylpyroglutamic acids
-
10.1016/S0040-4020(99)00710-3 1:CAS:528:DyaK1MXmsVOqtrw%3D
-
Soloshonok VA, Cai C, Hruby VJ, Meervelt LV (1999b) 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)
Tetrahedron
, vol.55
, pp. 12045-12058
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
Meervelt, L.V.4
-
28
-
-
0033402142
-
Asymmetric Michael addition reactions of chiral Ni(II)-complex of glycine with (N-trans-enoyl)oxazolidines: Improved reactivity and stereochemical outcome
-
10.1016/S0957-4166(99)00483-8 1:CAS:528:DC%2BD3cXkt1Wntg%3D%3D
-
Soloshonok VA, Cai C, Hruby VJ (1999c) Asymmetric Michael addition reactions of chiral Ni(II)-complex of glycine with (N-trans-enoyl)oxazolidines: improved reactivity and stereochemical outcome. Tetrahedron: Asymm 10:4265-4269
-
(1999)
Tetrahedron: Asymm
, vol.10
, pp. 4265-4269
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
-
29
-
-
0034704633
-
(S)- or (R)-3-(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
-
10754676 10.1021/ol990402f 1:CAS:528:DC%2BD3cXht1Kjsbs%3D
-
Soloshonok VA, Cai C, Hruby VJ (2000a) (S)- or (R)-3-(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 Lett 2:747-750
-
(2000)
Org Lett
, vol.2
, pp. 747-750
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
-
30
-
-
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
-
10.1016/S0040-4039(00)01737-8 1:CAS:528:DC%2BD3cXovFOmsbc%3D
-
Soloshonok VA, Cai C, Hruby VJ (2000b) 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)
Tetrahedron Lett
, vol.41
, pp. 9645-9649
-
-
Soloshonok, V.A.1
Cai, C.2
Hruby, V.J.3
-
31
-
-
0035825745
-
Asymmetric synthesis of α, β-dialkyl-α-phenylalanines via direct alkylation of a chiral alanine derivative with racemic α-alkylbenzyl bromides. A case of high enantiomer differentiation at room temperature
-
11428009 10.1021/ol000330o 1:CAS:528:DC%2BD3MXivVahtg%3D%3D
-
Soloshonok VA, Tang X, Hruby VJ, Meervelt LV (2001a) Asymmetric synthesis of α, β-dialkyl-α-phenylalanines via direct alkylation of a chiral alanine derivative with racemic α-alkylbenzyl bromides. A case of high enantiomer differentiation at room temperature. Org Lett 3:341-343
-
(2001)
Org Lett
, vol.3
, pp. 341-343
-
-
Soloshonok, V.A.1
Tang, X.2
Hruby, V.J.3
Meervelt, L.V.4
-
32
-
-
0035939193
-
Large-scale asymmetric synthesis of novel sterically constrained 2′,6′-dimethyl- and α,2′,6′-trimethyltyrosine and -phenylalanine derivatives via alkylation of chiral equivalents of nucleophilic glycine and alanine
-
10.1016/S0040-4020(01)00504-X 1:CAS:528:DC%2BD3MXltlOhs7c%3D
-
Soloshonok VA, Tang X, Hruby VJ (2001b) Large-scale asymmetric synthesis of novel sterically constrained 2′,6′-dimethyl- and α,2′,6′-trimethyltyrosine and -phenylalanine derivatives via alkylation of chiral equivalents of nucleophilic glycine and alanine. Tetrahedron 57:6375-6382
-
(2001)
Tetrahedron
, vol.57
, pp. 6375-6382
-
-
Soloshonok, V.A.1
Tang, X.2
Hruby, V.J.3
-
33
-
-
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-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: Practical method for preparation of beta-substituted pyroglutamic acids and prolines
-
15255725 10.1021/jo0495438 1:CAS:528:DC%2BD2cXltVCnsbk%3D
-
Soloshonok VA, Ueki H, Tiwari R, Cai C, Hruby VJ (2004) 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-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: practical method for preparation of beta-substituted pyroglutamic acids and prolines. J Org Chem 69:4984-4990
-
(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
-
34
-
-
12444311634
-
Application of modular nucleophilic glycine equivalents for truly practical asymmetric synthesis of β-substituted pyroglutamic acids
-
10.1016/j.tetlet.2004.12.093 1:CAS:528:DC%2BD2MXnsVGisA%3D%3D
-
Soloshonok VA, Ueki H, Ellis TK, Yamada T, Ohfune Y (2005a) Application of modular nucleophilic glycine equivalents for truly practical asymmetric synthesis of β-substituted pyroglutamic acids. Tetrahedron Lett 46:1107-1110
-
(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
-
35
-
-
27544463710
-
Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of β-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity
-
16248672 10.1021/ja0535561 1:CAS:528:DC%2BD2MXhtVylsr%2FJ
-
Soloshonok VA, Cai C, Yamada T, Ueki H, Ohfune Y, Hruby VJ (2005b) Michael addition reactions between chiral equivalents of a nucleophilic glycine and (S)- or (R)-3-[(E)-enoyl]-4-phenyl-1,3-oxazolidin-2-ones as a general method for efficient preparation of β-substituted pyroglutamic acids. Case of topographically controlled stereoselectivity. J Am Chem Soc 127:15296-15303
-
(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
-
36
-
-
33646804903
-
Operationally convenient, efficient asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via methylene dimerization of chiral glycine equivalents with dichloromethane
-
10.1016/j.tet.2006.04.023 1:CAS:528:DC%2BD28Xlt12ntbs%3D
-
Soloshonok VA, Yamada T, Ueki H, Moore AM, Cook TK, Arbogast KL, Soloshonok AV, Martin CH, Ohfune Y (2006) Operationally convenient, efficient asymmetric synthesis of enantiomerically pure 4-aminoglutamic acids via methylene dimerization of chiral glycine equivalents with dichloromethane. Tetrahedron 62:6412-6419
-
(2006)
Tetrahedron
, vol.62
, pp. 6412-6419
-
-
Soloshonok, V.A.1
Yamada, T.2
Ueki, H.3
Moore, A.M.4
Cook, T.K.5
Arbogast, K.L.6
Soloshonok, A.V.7
Martin, C.H.8
Ohfune, Y.9
-
37
-
-
38349142808
-
Asymmetric Diels-Alder reaction of aminodienes with a nonracemic acrylate bound to rink resin: A comparison of these reactions with their solution-state analogues
-
10.1002/ejoc.200700677
-
Songis O, Geant PY, Sautrey G, Martinez J, Calmes M (2008) Asymmetric Diels-Alder reaction of aminodienes with a nonracemic acrylate bound to rink resin: a comparison of these reactions with their solution-state analogues. Eur J Org Chem 2008:308-318
-
(2008)
Eur J Org Chem
, vol.2008
, pp. 308-318
-
-
Songis, O.1
Geant, P.Y.2
Sautrey, G.3
Martinez, J.4
Calmes, M.5
-
38
-
-
30744456747
-
Recent advances in natural product synthesis by using intramolecular Diels-Alder reactions
-
16351062 10.1021/cr040632u 1:CAS:528:DC%2BD2MXhtFahs7%2FF
-
Takao K, Munakata R, Tadano K (2005) Recent advances in natural product synthesis by using intramolecular Diels-Alder reactions. Chem Rev 105:4779-4807
-
(2005)
Chem Rev
, vol.105
, pp. 4779-4807
-
-
Takao, K.1
Munakata, R.2
Tadano, K.3
-
39
-
-
0034725677
-
Convenient, asymmetric synthesis of enantiomerically pure 2′,6′-dimethyltyrosine (DMT) via alkylation of chiral equivalent of nucleophilic glycine
-
10.1016/S0957-4166(00)00250-0 1:CAS:528:DC%2BD3cXlvVKmsb8%3D
-
Tang X, Soloshonok VA, Hruby VJ (2000) Convenient, asymmetric synthesis of enantiomerically pure 2′,6′-dimethyltyrosine (DMT) via alkylation of chiral equivalent of nucleophilic glycine. Tetrahedron: Asymm 11:2917-2925
-
(2000)
Tetrahedron: Asymm
, vol.11
, pp. 2917-2925
-
-
Tang, X.1
Soloshonok, V.A.2
Hruby, V.J.3
-
40
-
-
0037911550
-
Efficient large-scale synthesis of picolinic acid-derived Nickel(II) complexes of glycine
-
10.1002/ejoc.200200688
-
Ueki H, Ellis TK, Martin CH, Soloshonok VA (2003a) Efficient large-scale synthesis of picolinic acid-derived Nickel(II) complexes of glycine. Eur J Org Chem 2003:1954-1957
-
(2003)
Eur J Org Chem
, vol.2003
, pp. 1954-1957
-
-
Ueki, H.1
Ellis, T.K.2
Martin, C.H.3
Soloshonok, V.A.4
-
41
-
-
0042338452
-
Improved synthesis of proline-derived Ni(II) complexes of glycine: Versatile chiral equivalents of nucleophilic glycine for general asymmetric synthesis of α-amino acids
-
12946159 10.1021/jo0301494 1:CAS:528:DC%2BD3sXmtVSls78%3D
-
Ueki H, Ellis TK, Martin CH, Bolene SB, Boettiger TU, Soloshonok VA (2003b) Improved synthesis of proline-derived Ni(II) complexes of glycine: versatile chiral equivalents of nucleophilic glycine for general asymmetric synthesis of α-amino acids. J Org Chem 68:7104-7107
-
(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
-
42
-
-
55249094794
-
Highly enantio- and diastereoselective mannich reactions of chiral Ni(II) glycinates with amino sulfones. Efficient asymmetric synthesis of aromatic α, β-diamino acids
-
18844412 10.1021/jo8019169 1:CAS:528:DC%2BD1cXht1emsbjP
-
Wang J, Shi T, Deng G, Jiang H, Liu H (2008) Highly enantio- and diastereoselective mannich reactions of chiral Ni(II) glycinates with amino sulfones. Efficient asymmetric synthesis of aromatic α, β-diamino acids. J Org Chem 73:8563-8570
-
(2008)
J Org Chem
, vol.73
, pp. 8563-8570
-
-
Wang, J.1
Shi, T.2
Deng, G.3
Jiang, H.4
Liu, H.5
-
43
-
-
78651481203
-
Asymmetric synthesis of sterically and electronically demanding linear ω-trifluoromethyl containing amino acids via alkylation of chiral equivalents of nucleophilic glycine and alanine
-
21182272 10.1021/jo102031b 1:CAS:528:DC%2BC3cXhs1SrsLfP
-
Wang J, Lin D, Zhou S, Soloshonok VA, Liu H (2011) Asymmetric synthesis of sterically and electronically demanding linear ω-trifluoromethyl containing amino acids via alkylation of chiral equivalents of nucleophilic glycine and alanine. J Org Chem 76:684-687
-
(2011)
J Org Chem
, vol.76
, pp. 684-687
-
-
Wang, J.1
Lin, D.2
Zhou, S.3
Soloshonok, V.A.4
Liu, H.5
-
44
-
-
0034605848
-
Diels-Alder approaches to ring-functionalized cyclic β-amino acids
-
10.1016/S0040-4039(00)01576-8 1:CAS:528:DC%2BD3cXovVWksbo%3D
-
Wipf P, Wang X (2000) Diels-Alder approaches to ring-functionalized cyclic β-amino acids. Tetrahedron Lett 41:8747-8751
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 8747-8751
-
-
Wipf, P.1
Wang, X.2
-
45
-
-
33845976663
-
Efficient asymmetric synthesis of novel 4-substituted and configurationally stable analogues of thalidomide
-
17107088 10.1021/ol0623668 1:CAS:528:DC%2BD28XhtFehur3N
-
Yamada T, Okada T, Sakaguchi K, Ohfune Y, Ueki H, Soloshonok VA (2006) Efficient asymmetric synthesis of novel 4-substituted and configurationally stable analogues of thalidomide. Org Lett 8:5625-5628
-
(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
|