-
1
-
-
2842610709
-
Biomimetic chemistry and artificial enzymes: Catalysis by design
-
Breslow R (1995) Biomimetic chemistry and artificial enzymes: Catalysis by design. Acc Chem Res 28:146-153.
-
(1995)
Acc Chem Res
, vol.28
, pp. 146-153
-
-
Breslow, R.1
-
2
-
-
38349112828
-
Asymmetric catalysis mediated by synthetic peptides
-
Davie EAC, Mennen SM, Xu Y, Miller SJ (2007) Asymmetric catalysis mediated by synthetic peptides. Chem Rev 107:5759-5812.
-
(2007)
Chem Rev
, vol.107
, pp. 5759-5812
-
-
Davie, E.A.C.1
Mennen, S.M.2
Xu, Y.3
Miller, S.J.4
-
3
-
-
4143141139
-
In search of peptide-based catalysts for asymmetric organic synthesis
-
Miller SJ (2004) In search of peptide-based catalysts for asymmetric organic synthesis. Acc Chem Res 37:601-610.
-
(2004)
Acc Chem Res
, vol.37
, pp. 601-610
-
-
Miller, S.J.1
-
4
-
-
41949119312
-
Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins - a rational approach
-
Wiesner M, Revell JD, Wennemers H (2008) Tripeptides as efficient asymmetric catalysts for 1,4-addition reactions of aldehydes to nitroolefins - a rational approach. Angew Chem Int Ed 47:1871-1874.
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 1871-1874
-
-
Wiesner, M.1
Revell, J.D.2
Wennemers, H.3
-
5
-
-
0021200412
-
Chiral selection in poly (C)-directed synthesis of oligo (G)
-
Joyce GF, et al. (1984) Chiral selection in poly (C)-directed synthesis of oligo (G). Nature 310:602-604.
-
(1984)
Nature
, vol.310
, pp. 602-604
-
-
Joyce, G.F.1
-
6
-
-
0037012440
-
Characterization of an RNA active site: Interactions between a Diels-Alderase ribozyme and its substrates and products
-
DOI 10.1021/ja0167405
-
Stuhlmann F, Jäschke A (2002) Characterization of an RNA active site: Interactions between a diels-alderase ribozyme and its substrates and products. J Am Chem Soc 124:3238-3244. (Pubitemid 34270362)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.13
, pp. 3238-3244
-
-
Stuhlmann, F.1
Jaschke, A.2
-
8
-
-
51349111679
-
DNA-based asymmetric catalysis: Sequence-dependent rate acceleration and enantioselectivity
-
Boersma AJ, Klijin JE, Feringa BL, Roelfes G (2008) DNA-based asymmetric catalysis: Sequence-dependent rate acceleration and enantioselectivity. J Am Chem Soc 130:11783-11790.
-
(2008)
J Am Chem Soc
, vol.130
, pp. 11783-11790
-
-
Boersma, A.J.1
Klijin, J.E.2
Feringa, B.L.3
Roelfes, G.4
-
9
-
-
0542421525
-
Foldamers: A manifesto
-
Gellman SH (1998) Foldamers: A manifesto. Acc Chem Res 31:173-180.
-
(1998)
Acc Chem Res
, vol.31
, pp. 173-180
-
-
Gellman, S.H.1
-
10
-
-
0035542909
-
A field guide to foldamers
-
Hill DJ, Mio MJ, Prince RB, Hughes TS, Moore JS (2001) A field guide to foldamers. Chem Rev 101:3893-4011.
-
(2001)
Chem Rev
, vol.101
, pp. 3893-4011
-
-
Hill, D.J.1
Mio, M.J.2
Prince, R.B.3
Hughes, T.S.4
Moore, J.S.5
-
11
-
-
36849057990
-
-
Hecht S, Huc I, eds (Wiley-VCH, Weinheim, Germany).
-
Hecht S, Huc I, eds (2007) Foldamers: Structure, Properties, and Applications (Wiley-VCH, Weinheim, Germany).
-
(2007)
Foldamers: Structure, Properties, and Applications
-
-
-
12
-
-
57149097169
-
β-Peptidic peptidomimetics
-
Seebach D, Cardiner J (2008) β-Peptidic peptidomimetics. Acc Chem Res 41:1366-1375.
-
(2008)
Acc Chem Res
, vol.41
, pp. 1366-1375
-
-
Seebach, D.1
Cardiner, J.2
-
13
-
-
0032515982
-
Sequence-specific polypeptoids: A diverse family of heteropolymers with stable secondary structure
-
DOI 10.1073/pnas.95.8.4303
-
Kirshenbaum K, et al. (1998) Sequence-specific polypeptoids: A diverse family of heteropolymers with stable secondary structure. Proc Natl Acad Sci USA 95:4303-4308. (Pubitemid 28207907)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.8
, pp. 4303-4308
-
-
Kirshenbaum, K.1
Barron, A.E.2
Goldsmith, R.A.3
Armand, P.4
Bradley, E.K.5
Truong, K.T.V.6
Dill, K.A.7
Cohen, F.E.8
Zuckermann, R.N.9
-
14
-
-
0034835809
-
Peptoid oligomers with R-chiral, aromatic side chains: Sequence requirements for the formation of stable peptoid helices
-
DOI 10.1021/ja003154n
-
Wu CW, Sanborn TJ, Huang K, Zuckermann RN, Barron AE (2001) Peptoid oligomers with R-chiral, aromatic side chains: Sequence requirements for the formation of stable peptoid helices. J Am Chem Soc 123:6778-6784. (Pubitemid 32884537)
-
(2001)
Journal of the American Chemical Society
, vol.123
, Issue.28
, pp. 6778-6784
-
-
Wu, C.W.1
Sanborn, T.J.2
Huang, K.3
Zuckermann, R.N.4
Barron, A.E.5
-
15
-
-
0242299241
-
Structural and spectroscopic studies of peptoid oligomers with alpha-chiral aliphatic side chains
-
Wu CW, et al. (2003) Structural and spectroscopic studies of peptoid oligomers with alpha-chiral aliphatic side chains. J Am Chem Soc 125:13525-13530.
-
(2003)
J Am Chem Soc
, vol.125
, pp. 13525-13530
-
-
Wu, C.W.1
-
16
-
-
57549101729
-
Peptoid architectures: Elaboration, actuation and application
-
Yoo B, Kirshenbaum K (2008) Peptoid architectures: Elaboration, actuation and application. Curr Opin Chem Bio 12:714-721.
-
(2008)
Curr Opin Chem Bio
, vol.12
, pp. 714-721
-
-
Yoo, B.1
Kirshenbaum, K.2
-
17
-
-
0036738419
-
A green, catalytic oxidation of alcohols
-
Sheldon RA, Arends IWCE, Brink G-JT, Dijksman A (2002) A green, catalytic oxidation of alcohols. Acc Chem Res 35:774-781.
-
(2002)
Acc Chem Res
, vol.35
, pp. 774-781
-
-
Sheldon, R.A.1
Arends, I.W.C.E.2
Brink, G.-J.T.3
Dijksman, A.4
-
18
-
-
5144233845
-
Organocatalytic oxidations mediated by nitroxyl radicals
-
Sheldon RA, Arends IWCE (2004) Organocatalytic oxidations mediated by nitroxyl radicals. Adv Synth Catal 346:1051-1071.
-
(2004)
Adv Synth Catal
, vol.346
, pp. 1051-1071
-
-
Sheldon, R.A.1
Arends, I.W.C.E.2
-
19
-
-
33846104288
-
Chiral N-oxides in asymmetric catalysis
-
Malkov AV, Kocovsky P (2007) Chiral N-oxides in asymmetric catalysis. Eur J Org Chem 1:29-36.
-
(2007)
Eur J Org Chem
, vol.1
, pp. 29-36
-
-
Malkov, A.V.1
Kocovsky, P.2
-
20
-
-
0035526027
-
Synthetic applications of nonmetal catalysts for homogeneous oxidations
-
DOI 10.1021/cr000019k
-
Adam W, Saha-Möller CR, Ganeshpure PA (2001) Synthetic applications of nonmetal catalysts for homogeneous oxidations. Chem Rev 101:3499-3548. (Pubitemid 35373044)
-
(2001)
Chemical Reviews
, vol.101
, Issue.11
, pp. 3499-3548
-
-
Adam, W.1
Saha-Moller, C.R.2
Ganeshpure, P.A.3
-
21
-
-
0037416315
-
Chiral-Mn(salen) complex catalyzed kinetic resolution of secondary alcohols in water
-
Wei S, Hongwang W, Chungu X, Jingwei L, Peiqing Z (2003) Chiral-Mn(salen) complex catalyzed kinetic resolution of secondary alcohols in water. Angew Chem Int Ed 42:1042-1044.
-
(2003)
Angew Chem Int Ed
, vol.42
, pp. 1042-1044
-
-
Wei, S.1
Hongwang, W.2
Chungu, X.3
Jingwei, L.4
Peiqing, Z.5
-
22
-
-
56749149527
-
Structural features and reactivity of (sparteine)PdCl2: A model for selectivity in the oxidative kinetic resolution of secondary alcohols
-
Trend RM, Stoltz BM (2008) Structural features and reactivity of (sparteine)PdCl2: A model for selectivity in the oxidative kinetic resolution of secondary alcohols. J Am Chem Soc 130:15957-15966.
-
(2008)
J Am Chem Soc
, vol.130
, pp. 15957-15966
-
-
Trend, R.M.1
Stoltz, B.M.2
-
23
-
-
33645532122
-
Ligand-modulated palladium-catalyzed aerobic alcohol oxidations
-
Sigman MS, Jensen DR (2006) Ligand-modulated palladium-catalyzed aerobic alcohol oxidations. Acc Chem Res 39:221-229.
-
(2006)
Acc Chem Res
, vol.39
, pp. 221-229
-
-
Sigman, M.S.1
Jensen, D.R.2
-
24
-
-
52449100159
-
Natural products as inspiration for the development of asymmetric catalysis
-
Mohr JT, Krout MR, Stoltz BM (2008) Natural products as inspiration for the development of asymmetric catalysis. Nature 455:323-332.
-
(2008)
Nature
, vol.455
, pp. 323-332
-
-
Mohr, J.T.1
Krout, M.R.2
Stoltz, B.M.3
-
25
-
-
37049077879
-
Enzymic preparation of enantiomerically pure secondary alcohols. Ester synthesis by irreversible acyl transfer using a highly selective ester hydrolase from Pseudomonas sp: An attractive alternative to ester hydrolysis
-
Laumen K, Breitgoff D, Schneider MP (1988) Enzymic preparation of enantiomerically pure secondary alcohols. Ester synthesis by irreversible acyl transfer using a highly selective ester hydrolase from Pseudomonas sp: An attractive alternative to ester hydrolysis. Chem Commun, 1459-1461.
-
(1988)
Chem Commun
, pp. 1459-1461
-
-
Laumen, K.1
Breitgoff, D.2
Schneider, M.P.3
-
26
-
-
33845282179
-
Fast and selective oxidation of alcohols to aldehydes or to carboxylic acids and secondary alcohols to ketones mediated by oxoammonium salts under two-phase conditions
-
Anelli PL, Biffi C, Montanari F, Quici S (1987) Fast and selective oxidation of alcohols to aldehydes or to carboxylic acids and secondary alcohols to ketones mediated by oxoammonium salts under two-phase conditions. J Org Chem 52:2559-2562.
-
(1987)
J Org Chem
, vol.52
, pp. 2559-2562
-
-
Anelli, P.L.1
Biffi, C.2
Montanari, F.3
Quici, S.4
-
27
-
-
0037016582
-
Nitroxyl peptides as catalysts of enantioselective oxidations
-
DOI 10.1002/1521-3765(20020104)8:1<84::AID-CHEM84>3.0.CO;2-N
-
Formaggio F, et al. (2002) Nitroxyl peptides as catalysts of enantioselective oxidations. Chem Eur J 8:84-93. (Pubitemid 34087370)
-
(2002)
Chemistry - a European Journal
, vol.8
, Issue.1
, pp. 84-93
-
-
Formaggio, F.1
Bonchio, M.2
Crisma, M.3
Peggion, C.4
Mezzato, S.5
Polese, A.6
Barazza, A.7
Antonello, S.8
Maran, F.9
Broxterman, Q.B.10
Kaptein, B.11
Kamphuis, J.12
Vitale, R.M.13
Saviano, M.14
Benedetti, E.15
Toniolo, C.16
-
28
-
-
52049096917
-
Palladium-catalyzed enantioselective oxidation of chiral secondary alcohols: Access to both enantiomeric series
-
Ebner DC, et al. (2008) Palladium-catalyzed enantioselective oxidation of chiral secondary alcohols: Access to both enantiomeric series. Angew Chem Int Ed 47:6367-6370.
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 6367-6370
-
-
Ebner, D.C.1
-
29
-
-
33846197463
-
Characterizing the structure and dynamics of folded oligomers: Pulsed ESR studies of peptoid helices
-
Fafarman AT, Borbat PP, Freed JH, Kirshenbaum K (2006) Characterizing the structure and dynamics of folded oligomers: Pulsed ESR studies of peptoid helices. Chem Commun, 377-379.
-
(2006)
Chem Commun
, pp. 377-379
-
-
Fafarman, A.T.1
Borbat, P.P.2
Freed, J.H.3
Kirshenbaum, K.4
-
30
-
-
0034358478
-
The Julia-Colonna type asymmetric epoxidation reaction catalyzed by soluble oligo-L-leucines containing an α-aminoisobutyric acid residue: Importance of helical structure of the catalyst on asymmetric induction
-
Takagi R, Shiraki A, Manabe T, Kojima S, Ohkata K (2000) The Julia-Colonna type asymmetric epoxidation reaction catalyzed by soluble oligo-L-leucines containing an α-aminoisobutyric acid residue: Importance of helical structure of the catalyst on asymmetric induction. Chem Lett 29:366-367.
-
(2000)
Chem Lett
, vol.29
, pp. 366-367
-
-
Takagi, R.1
Shiraki, A.2
Manabe, T.3
Kojima, S.4
Ohkata, K.5
-
31
-
-
0033596302
-
A biomimetic approach to asymmetric acyl transfer catalysis
-
DOI 10.1021/ja9931776
-
Jarvo ER, Copeland GT, Papaioannou N, Bonitatebus PJ, Jr, Miller SJ (1999) A biomimetic approach to asymmetric acyl transfer catalysis. J Am Chem Soc 121:11638-11643. (Pubitemid 30032740)
-
(1999)
Journal of the American Chemical Society
, vol.121
, Issue.50
, pp. 11638-11643
-
-
Jarvo, E.R.1
Copeland, G.T.2
Papaioannou, N.3
Bonitatebus Jr., P.J.4
Miller, S.J.5
-
32
-
-
33645457905
-
The small peptide-catalyzed direct asymmetric aldol reaction in water
-
Dziedzic P, Zou W, Háfren J, Córdova A (2006) The small peptide-catalyzed direct asymmetric aldol reaction in water. Org Biomol Chem 4:38-40.
-
(2006)
Org Biomol Chem
, vol.4
, pp. 38-40
-
-
Dziedzic, P.1
Zou, W.2
Háfren, J.3
Córdova, A.4
-
33
-
-
54249095628
-
3-PIP-catalyzed kinetic resolution of secondary benzylic alcohols
-
3-PIP-catalyzed kinetic resolution of secondary benzylic alcohols. J Am Chem Soc 130:13836-13837.
-
(2008)
J Am Chem Soc
, vol.130
, pp. 13836-13837
-
-
Li, X.1
Liu, P.2
Houk, K.N.3
Birman, V.B.4
-
34
-
-
3042721763
-
Structure-selectivity relationships and structure for a peptide-based enantioselective acylation catalyst
-
Fierman MB, O'Leary DJ, Steinmetz WE, Miller SJ (2004) Structure-selectivity relationships and structure for a peptide-based enantioselective acylation catalyst. J Am Chem Soc 126:6967-6971.
-
(2004)
J Am Chem Soc
, vol.126
, pp. 6967-6971
-
-
Fierman, M.B.1
O'Leary, D.J.2
Steinmetz, W.E.3
Miller, S.J.4
-
35
-
-
34247362490
-
Foldamers as versatile frameworks for the design and evolution of function
-
DOI 10.1038/nchembio876, PII NCHEMBIO876
-
Goodman CM, Choi S, Shandler S, DeGrado WF (2007) Foldamers as versatile frameworks for the design and evolution of function. Nat Chem Biol 3:252-262. (Pubitemid 46628637)
-
(2007)
Nature Chemical Biology
, vol.3
, Issue.5
, pp. 252-262
-
-
Goodman, C.M.1
Choi, S.2
Shandler, S.3
Degrado, W.F.4
-
36
-
-
23744462184
-
Folding a nonbiological polymer into a compact multihelical structure
-
Lee B-C, Zuckermann RN, Dill KA (2005) Folding a nonbiological polymer into a compact multihelical structure. J Am Chem Soc 127:10999-11009.
-
(2005)
J Am Chem Soc
, vol.127
, pp. 10999-11009
-
-
Lee, B.-C.1
Zuckermann, R.N.2
Dill, K.A.3
-
37
-
-
46949089574
-
Biomimetic nanostructures: Creating a high-affinity zinc-binding site in a folded nonbiological polymer
-
Lee B-C, Chu TK, Dill KA, Zuckermann RN (2008) Biomimetic nanostructures: Creating a high-affinity zinc-binding site in a folded nonbiological polymer. J Am Chem Soc 130:8847-8855.
-
(2008)
J Am Chem Soc
, vol.130
, pp. 8847-8855
-
-
Lee, B.-C.1
Chu, T.K.2
Dill, K.A.3
Zuckermann, R.N.4
-
39
-
-
58349089455
-
A rationally designed aldolase foldamer
-
Müller MM, Windsor MA, Pomerantz WC, Gellman SH, Hilvert D (2009) A rationally designed aldolase foldamer. Angew Chem Int Ed 48:922-925.
-
(2009)
Angew Chem Int Ed
, vol.48
, pp. 922-925
-
-
Müller, M.M.1
Windsor, M.A.2
Pomerantz, W.C.3
Gellman, S.H.4
Hilvert, D.5
|