-
1
-
-
33748766864
-
The organic approach to asymmetric catalysis
-
List, B. & Yang, J. W. The organic approach to asymmetric catalysis. Science 313, 1584-1586 (2006).
-
(2006)
Science
, vol.313
, pp. 1584-1586
-
-
List, B.1
Yang, J.W.2
-
2
-
-
38349100690
-
Asymmetric enamine catalysis
-
Mukherjee, S., Yang, J. W., Hoffmann, S. & List, B. Asymmetric enamine catalysis. Chem. Rev. 107, 5471-5569 (2007).
-
(2007)
Chem. Rev
, vol.107
, pp. 5471-5569
-
-
Mukherjee, S.1
Yang, J.W.2
Hoffmann, S.3
List, B.4
-
3
-
-
0037059471
-
Proline-catalyzed one-step asymmetric synthesis of 5-hydroxy (2E)-hexenal from acetaldehyde
-
Córdova, A., Notz, W. & Barbas, C. F. III. Proline-catalyzed one-step asymmetric synthesis of 5-hydroxy (2E)-hexenal from acetaldehyde. J. Org. Chem. 67, 301-303 (2002).
-
(2002)
J. Org. Chem
, vol.67
, pp. 301-303
-
-
Córdova, A.1
Notz, W.2
Barbas III, C.F.3
-
6
-
-
0035921177
-
Continuous production of (R)-phenylacetylcarbinol in an enzyme-membrane reactor using a potent mutant of pyruvate decarboxylase from Zymomonas mobilis
-
Goetz, G., Iwan, P., Hauer, B., Breuer, M. & Pohl, M. Continuous production of (R)-phenylacetylcarbinol in an enzyme-membrane reactor using a potent mutant of pyruvate decarboxylase from Zymomonas mobilis. Biotechnol. Bioeng. 74, 317-325 (2001).
-
(2001)
Biotechnol. Bioeng
, vol.74
, pp. 317-325
-
-
Goetz, G.1
Iwan, P.2
Hauer, B.3
Breuer, M.4
Pohl, M.5
-
7
-
-
0000402252
-
Asymmetric Michael additions via SAMP-/RAMP-hydrazones enantioselective synthesis of β-substituted δ-oxopentanoates and δ-lactones
-
Enders, D. & Rendenbach, B. E. M. Asymmetric Michael additions via SAMP-/RAMP-hydrazones enantioselective synthesis of β-substituted δ-oxopentanoates and δ-lactones. Chem. Ber. 120, 1223-1227 (1987).
-
(1987)
Chem. Ber
, vol.120
, pp. 1223-1227
-
-
Enders, D.1
Rendenbach, B.E.M.2
-
8
-
-
28044459433
-
Lewis base catalyzed enantioselective aldol addition of acetaldehyde-derived silyl enol ether to aldehydes
-
Denmark, S. E. & Bui, T. Lewis base catalyzed enantioselective aldol addition of acetaldehyde-derived silyl enol ether to aldehydes. J. Org. Chem. 70, 10190-10193 (2005).
-
(2005)
J. Org. Chem
, vol.70
, pp. 10190-10193
-
-
Denmark, S.E.1
Bui, T.2
-
9
-
-
30744464122
-
Tris(trimethylsilyl)silyl-governed aldehyde cross-aldol cascade reaction
-
Boxer, M. B. & Yamamoto, H. Tris(trimethylsilyl)silyl-governed aldehyde cross-aldol cascade reaction. J. Am. Chem. Soc. 128, 48-49 (2006).
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 48-49
-
-
Boxer, M.B.1
Yamamoto, H.2
-
10
-
-
0034721440
-
The direct catalytic asymmetric three-component Mannich reaction
-
List, B. The direct catalytic asymmetric three-component Mannich reaction. J. Am. Chem. Soc. 122, 9336-9337 (2000).
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 9336-9337
-
-
List, B.1
-
11
-
-
33746079973
-
Asymmetric synthesis of (+)-polyoxamic acid via an efficient organocatalytic Mannich reaction as the key step
-
Enders, D. & Vrettou, M. Asymmetric synthesis of (+)-polyoxamic acid via an efficient organocatalytic Mannich reaction as the key step. Synthesis 2155-2158 (2006).
-
(2006)
Synthesis
, vol.2155-2158
-
-
Enders, D.1
Vrettou, M.2
-
12
-
-
33846550172
-
Proline-catalyzed Mannich reaction of aldehydes with N-Boc-imines
-
Yang, J. W., Stadler, M. & List, B. Proline-catalyzed Mannich reaction of aldehydes with N-Boc-imines. Angew. Chem. Int. Edn Engl. 46, 609-611 (2007).
-
(2007)
Angew. Chem. Int. Edn Engl
, vol.46
, pp. 609-611
-
-
Yang, J.W.1
Stadler, M.2
List, B.3
-
13
-
-
17344384874
-
Non-haemolytic β-amino-acid oligomers
-
Porter, E. A., Wang, X., Lee, H.-S., Weisblum, B. & Gellman, S. H. Non-haemolytic β-amino-acid oligomers. Nature 404, 565 (2000).
-
(2000)
Nature
, vol.404
, pp. 565
-
-
Porter, E.A.1
Wang, X.2
Lee, H.-S.3
Weisblum, B.4
Gellman, S.H.5
-
14
-
-
0033786668
-
14-helical secondary structures in water
-
14-helical secondary structures in water. Helv. Chim. Acta 83, 2115-2140 (2000).
-
(2000)
Helv. Chim. Acta
, vol.83
, pp. 2115-2140
-
-
Seebach, D.1
-
15
-
-
22944479941
-
Highly diastereoselective and enantioselective preparation of homoallylic amines: Application for the synthesis of β-amino acids and γ-lactams
-
Ramachandran, P. V. & Burghardt, T. E. Highly diastereoselective and enantioselective preparation of homoallylic amines: application for the synthesis of β-amino acids and γ-lactams. Chem. Eur. J. 11, 4387-4395 (2005).
-
(2005)
Chem. Eur. J
, vol.11
, pp. 4387-4395
-
-
Ramachandran, P.V.1
Burghardt, T.E.2
-
16
-
-
34248562082
-
2-amino acids via proline-catalyzed diastereoselective aminomethylation of aldehydes
-
2-amino acids via proline-catalyzed diastereoselective aminomethylation of aldehydes. J. Am. Chem. Soc. 129, 6050-6055 (2007).
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 6050-6055
-
-
Chi, Y.1
-
17
-
-
13544259815
-
Dapoxetine hydrochloride
-
Sorbera, L. A., Castañer, J. & Castañer, R. M. Dapoxetine hydrochloride. Drugs Fut. 29, 1201-1205 (2004).
-
(2004)
Drugs Fut
, vol.29
, pp. 1201-1205
-
-
Sorbera, L.A.1
Castañer, J.2
Castañer, R.M.3
-
18
-
-
34748923492
-
Enantioselective synthesis of (S)-dapoxetine
-
Siddiqui, S. A. & Srinivasan, K. V. Enantioselective synthesis of (S)-dapoxetine. Tetrahedr. Asymm. 18, 2099-2103 (2007).
-
(2007)
Tetrahedr. Asymm
, vol.18
, pp. 2099-2103
-
-
Siddiqui, S.A.1
Srinivasan, K.V.2
-
19
-
-
33745829823
-
Oxazinanones as chiral auxiliaries: Synthesis and evaluation in enolate alkylations and aldol reactions
-
Davies, S. G. et al. Oxazinanones as chiral auxiliaries: synthesis and evaluation in enolate alkylations and aldol reactions. Org. Biomol. Chem. 4, 2753-2768 (2006).
-
(2006)
Org. Biomol. Chem
, vol.4
, pp. 2753-2768
-
-
Davies, S.G.1
-
20
-
-
27644510382
-
Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum antihuman immunodeficiency virus type 1 activity
-
Dorr, P. et al. Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum antihuman immunodeficiency virus type 1 activity. Antimicrob. Agents Chemother. 49, 4721-4732 (2005).
-
(2005)
Antimicrob. Agents Chemother
, vol.49
, pp. 4721-4732
-
-
Dorr, P.1
-
21
-
-
20544475634
-
Initial synthesis of UK-427,857 (Maraviroc)
-
Price, D. A. et al. Initial synthesis of UK-427,857 (Maraviroc). Tetrahedr. Lett. 46, 5005-5007 (2005).
-
(2005)
Tetrahedr. Lett
, vol.46
, pp. 5005-5007
-
-
Price, D.A.1
-
22
-
-
0032514423
-
Synthesis and applications of nonracemic β-amino aldehydes to the asymmetric synthesis of piperdines: (+)-dihydropinidine
-
Davis, F. A. & Szewczyk, J. M. Synthesis and applications of nonracemic β-amino aldehydes to the asymmetric synthesis of piperdines: (+)-dihydropinidine. Tetrahedr. Lett. 39, 5951-5954 (1998).
-
(1998)
Tetrahedr. Lett
, vol.39
, pp. 5951-5954
-
-
Davis, F.A.1
Szewczyk, J.M.2
-
23
-
-
0001867685
-
-
ed. Pelletier, S. W, Wiley, New York
-
Fodor, G. B. & Colasanti, B. in Alkaloids: Chemical and Biological Perspectives (ed. Pelletier, S. W.) 1-90 (Wiley, New York, 1985).
-
(1985)
Alkaloids: Chemical and Biological Perspectives
, pp. 1-90
-
-
Fodor, G.B.1
Colasanti, B.2
-
24
-
-
33646511310
-
The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: Enantioselective synthesis of β-amino acids
-
Song, J., Wang, Y. & Deng, L. The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: enantioselective synthesis of β-amino acids. J. Am. Chem. Soc. 128, 6048-6049 (2006).
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 6048-6049
-
-
Song, J.1
Wang, Y.2
Deng, L.3
|