-
1
-
-
1442286555
-
-
For a review, see
-
For a review, see T. Miyazaki, X. Han-ja, H. Tokuyama, T. Fukuyama, Synlett 2004, 477-480.
-
(2004)
Synlett
, pp. 477-480
-
-
Miyazaki, T.1
Han-ja, X.2
Tokuyama, H.3
Fukuyama, T.4
-
2
-
-
0034006463
-
-
For a review, see
-
For a review, see M. Benaglia, M. Cinquini, F. Cozzi, Eur. J. Org. Chem. 2000, 563-572.
-
(2000)
Eur. J. Org. Chem
, pp. 563-572
-
-
Benaglia, M.1
Cinquini, M.2
Cozzi, F.3
-
3
-
-
33645451499
-
-
For reviews, see a
-
For reviews, see a) A. Hill, Nat. Prod. Rep. 2006, 23, 256-320;
-
(2006)
Nat. Prod. Rep
, vol.23
, pp. 256-320
-
-
Hill, A.1
-
5
-
-
33745211232
-
-
For examples, see a
-
For examples, see a) Y.-M. Zhang, J. Hurlbert, S. W. White, C. O. Rock, J. Biol. Chem. 2006, 281, 17390-17399;
-
(2006)
J. Biol. Chem
, vol.281
, pp. 17390-17399
-
-
Zhang, Y.-M.1
Hurlbert, J.2
White, S.W.3
Rock, C.O.4
-
6
-
-
7244239181
-
-
b) M. B. Austin, M. Izumikawa, M. E. Bowman, D. W. Udwary, J.-L. Ferrer, B. S. Moore, J. P. Noel, J. Biol. Chem. 2004, 279, 45162-45174;
-
(2004)
J. Biol. Chem
, vol.279
, pp. 45162-45174
-
-
Austin, M.B.1
Izumikawa, M.2
Bowman, M.E.3
Udwary, D.W.4
Ferrer, J.-L.5
Moore, B.S.6
Noel, J.P.7
-
7
-
-
0034526571
-
-
c) J. M. Jez, M. B. Austin, J.-L. Ferrer, M. E. Bowman, J. Schröder, J. P. Noel, Chem. Biol. 2000, 7, 919-930.
-
(2000)
Chem. Biol
, vol.7
, pp. 919-930
-
-
Jez, J.M.1
Austin, M.B.2
Ferrer, J.-L.3
Bowman, M.E.4
Schröder, J.5
Noel, J.P.6
-
8
-
-
0242559475
-
-
For metal-catalyzed Knoevenagel and Claisen condensations with MAHTs, see a
-
For metal-catalyzed Knoevenagel and Claisen condensations with MAHTs, see a) Y. Kobuke, J.-i. Yoshida, Tetrahedron Lett. 1978, 19, 367-370;
-
(1978)
Tetrahedron Lett
, vol.19
, pp. 367-370
-
-
Kobuke, Y.1
Yoshida, J.-I.2
-
10
-
-
34250642402
-
-
c) F. Berrué, S. Antoniotti, O. P. Thomas, P. Amade, Eur. J. Org. Chem. 2007, 1743-1748.
-
(2007)
Eur. J. Org. Chem
, pp. 1743-1748
-
-
Berrué, F.1
Antoniotti, S.2
Thomas, O.P.3
Amade, P.4
-
11
-
-
33846842435
-
-
For metal-catalyzed enantioselective aldol reactions with MAHTs, see a
-
For metal-catalyzed enantioselective aldol reactions with MAHTs, see a) K. C. Fortner, M. D. Shair, J. Am. Chem. Soc. 2007, 129, 1032-1033;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 1032-1033
-
-
Fortner, K.C.1
Shair, M.D.2
-
12
-
-
19744363827
-
-
b) D. Magdziak, G. Lalic, H. M. Lee, K. C. Fortner, A. D. Aloise, M. D. Shair, J. Am. Chem. Soc. 2005, 127, 7284-7285;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 7284-7285
-
-
Magdziak, D.1
Lalic, G.2
Lee, H.M.3
Fortner, K.C.4
Aloise, A.D.5
Shair, M.D.6
-
13
-
-
0037433513
-
-
c) G. Lalic, A. D. Aloise, M. D. Shair, J. Am. Chem. Soc. 2003, 125, 2852-2853;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 2852-2853
-
-
Lalic, G.1
Aloise, A.D.2
Shair, M.D.3
-
14
-
-
0842326656
-
-
d) S. Orlandi, M. Benaglia, F. Cozzi, Tetrahedron Lett. 2004, 45, 1747-1750.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 1747-1750
-
-
Orlandi, S.1
Benaglia, M.2
Cozzi, F.3
-
15
-
-
33846226531
-
-
For an intriguing recent report on the mimicry of Cys- and CoA-dependent enzymes by cysteine, see
-
For an intriguing recent report on the mimicry of Cys- and CoA-dependent enzymes by cysteine, see C. E. Aroyan, S. J. Miller, J. Am. Chem. Soc. 2007, 129, 256-257.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 256-257
-
-
Aroyan, C.E.1
Miller, S.J.2
-
16
-
-
34547186720
-
-
During the review process of this manuscript, an excellent report appeared in which cinchona alkaloid derivatives were successfully used as catalysts for asymmetric MAHT addition reactions to imines, see
-
During the review process of this manuscript, an excellent report appeared in which cinchona alkaloid derivatives were successfully used as catalysts for asymmetric MAHT addition reactions to imines, see A. Ricci, D. Pettersen, L. Bernardi, F. Fini, M. Fochi, R. Perez Herrera, V. Sgarzani, Adv. Synth. Catal. 2007, 349, 1037-1040.
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 1037-1040
-
-
Ricci, A.1
Pettersen, D.2
Bernardi, L.3
Fini, F.4
Fochi, M.5
Perez Herrera, R.6
Sgarzani, V.7
-
17
-
-
0001315449
-
-
For a study on the decarboxylation of malonic acid derivatives by bases, see
-
For a study on the decarboxylation of malonic acid derivatives by bases, see H. Brunner, J. Müller, J. Spitzer, Monatsh. Chem. 1996, 127, 845-858.
-
(1996)
Monatsh. Chem
, vol.127
, pp. 845-858
-
-
Brunner, H.1
Müller, J.2
Spitzer, J.3
-
18
-
-
34548712694
-
-
MAHTs with electron-poor aromatic substituents undergo decarboxylation faster than those bearing electron-rich aromatic substituents, see Ref, 5b] and the Supporting Information
-
MAHTs with electron-poor aromatic substituents undergo decarboxylation faster than those bearing electron-rich aromatic substituents, see Ref. [5b] and the Supporting Information.
-
-
-
-
19
-
-
33746277515
-
-
For reviews/books, see a
-
For reviews/books, see a) S. J. Connon, Chem. Eur. J. 2006, 12, 5418-5427;
-
(2006)
Chem. Eur. J
, vol.12
, pp. 5418-5427
-
-
Connon, S.J.1
-
21
-
-
33646468489
-
-
Angew. Chem. Int. Ed. 2006, 45, 1520-1543;
-
(2006)
Chem. Int. Ed
, vol.45
, pp. 1520-1543
-
-
Angew1
-
22
-
-
47749122232
-
-
Eds, A. Berkessel, H Gröger, Wiley-VCH, Weinheim
-
c) Asymmetric Organocatalysis (Eds.: A. Berkessel, H Gröger), Wiley-VCH, Weinheim, 2005.
-
(2005)
Asymmetric Organocatalysis
-
-
-
23
-
-
33846601028
-
-
For examples of catalysis by urea-functionalized cinchona alkaloids, see a B. Wang, F. Wu, Y. Wang, X. Liu, L. Deng, J. Am. Chem. Soc. 2007, 129, 768-769;
-
For examples of catalysis by urea-functionalized cinchona alkaloids, see a) B. Wang, F. Wu, Y. Wang, X. Liu, L. Deng, J. Am. Chem. Soc. 2007, 129, 768-769;
-
-
-
-
24
-
-
33847782578
-
-
b) J. Song, H.-W Shih, L. Deng, Org. Lett. 2007, 9, 603-606;
-
(2007)
Org. Lett
, vol.9
, pp. 603-606
-
-
Song, J.1
Shih, H.-W.2
Deng, L.3
-
25
-
-
33749520452
-
-
c) J. Wang, H. Li, L. Zu, W. Jiang, H. Xie, W. Duan, W. Wang, J. Am. Chem. Soc. 2006, 128, 12652-12653;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 12652-12653
-
-
Wang, J.1
Li, H.2
Zu, L.3
Jiang, W.4
Xie, H.5
Duan, W.6
Wang, W.7
-
26
-
-
33646511310
-
-
d) J. Song, Y. Wang, L. Deng, J. Am. Chem. Soc. 2006, 128, 6048-6049;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 6048-6049
-
-
Song, J.1
Wang, Y.2
Deng, L.3
-
27
-
-
33745672062
-
-
e) Y.-Q. Wang, J. Song, R. Hong, H. Li, L. Deng, J. Am. Chem. Soc. 2006, 128, 8156-8157;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 8156-8157
-
-
Wang, Y.-Q.1
Song, J.2
Hong, R.3
Li, H.4
Deng, L.5
-
28
-
-
33746212557
-
-
f) T. Marcelli, R. N. S. van der Haas, J. H. van Maarseveen, H. Hiemstra, Angew. Chem. 2006, 118, 943-945;
-
(2006)
Angew. Chem
, vol.118
, pp. 943-945
-
-
Marcelli, T.1
van der Haas, R.N.S.2
van Maarseveen, J.H.3
Hiemstra, H.4
-
29
-
-
32044463560
-
-
Angew. Chem. Int. Ed. 2006, 45, 929-931;
-
(2006)
Chem. Int. Ed
, vol.45
, pp. 929-931
-
-
Angew1
-
30
-
-
33749008198
-
-
g) S. H. McCooey, T. McCabe, S. J. Connon, J. Org. Chem. 2006, 71, 7494-7497;
-
(2006)
J. Org. Chem
, vol.71
, pp. 7494-7497
-
-
McCooey, S.H.1
McCabe, T.2
Connon, S.J.3
-
31
-
-
28944454980
-
-
h) L. Bernardi, F. Fini, R. P. Herrera, A. Ricci, V. Sgarzani, Tetrahedron 2006, 62, 375-380;
-
(2006)
Tetrahedron
, vol.62
, pp. 375-380
-
-
Bernardi, L.1
Fini, F.2
Herrera, R.P.3
Ricci, A.4
Sgarzani, V.5
-
33
-
-
33646146207
-
-
j) A. E. Mattson, A. M. Zuhl, T. E. Reynolds, K. A. Scheidt, J. Am. Chem. Soc. 2006, 128, 4932-4933;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 4932-4933
-
-
Mattson, A.E.1
Zuhl, A.M.2
Reynolds, T.E.3
Scheidt, K.A.4
-
34
-
-
84962467066
-
-
k) A. Hamza, G. Schubert, T. Soós, I. Pápai, J. Am. Chem. Soc. 2006, 128, 13151-13160;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 13151-13160
-
-
Hamza, A.1
Schubert, G.2
Soós, T.3
Pápai, I.4
-
36
-
-
15444366940
-
-
m) B.-J. Li, L. Jiang, M. Liu, Y.-C. Chen, L.-S. Ding, Y. Wu, Synlett 2005, 603-606;
-
(2005)
Synlett
, pp. 603-606
-
-
Li, B.-J.1
Jiang, L.2
Liu, M.3
Chen, Y.-C.4
Ding, L.-S.5
Wu, Y.6
-
37
-
-
19544393388
-
-
n) B. Vakulya, S. Varga, A. Csámpai, T. Soós, Org. Lett. 2005, 7, 1967-1969;
-
(2005)
Org. Lett
, vol.7
, pp. 1967-1969
-
-
Vakulya, B.1
Varga, S.2
Csámpai, A.3
Soós, T.4
-
39
-
-
26844450640
-
-
Angew. Chem. Int. Ed. 2005, 44, 6367-6370.
-
(2005)
Chem. Int. Ed
, vol.44
, pp. 6367-6370
-
-
Angew1
-
40
-
-
0013059152
-
-
For another example of improved enantioselectivity in EVE, see
-
For another example of improved enantioselectivity in EVE, see K. Gademann, D. E. Chavez, E. N. Jacobsen, Angew. Chem. 2002, 114, 3185-3187;
-
(2002)
Angew. Chem
, vol.114
, pp. 3185-3187
-
-
Gademann, K.1
Chavez, D.E.2
Jacobsen, E.N.3
-
41
-
-
0037118895
-
-
Angew. Chem. Int. Ed. 2002, 41, 3059-3061.
-
(2002)
Chem. Int. Ed
, vol.41
, pp. 3059-3061
-
-
Angew1
-
42
-
-
34548811177
-
-
Over the course of the reaction an increase in the enantioselectivity was observed
-
Over the course of the reaction an increase in the enantioselectivity was observed.
-
-
-
-
43
-
-
34347357692
-
-
For syntheses of rolipram, see a
-
For syntheses of rolipram, see a) D. Albrecht, T. Bach, Synlett 2007, 1557-1560;
-
(2007)
Synlett
, pp. 1557-1560
-
-
Albrecht, D.1
Bach, T.2
-
44
-
-
13244298300
-
-
A. L. L. Garcia, M. J. S. Carpes, A. C. B. M. de Oca, M. A. G. dos Santos, C. C. Santana, C. R. D. Correia, J. Org. Chem. 2005, 70, 1050-1053, and references therein;
-
b) A. L. L. Garcia, M. J. S. Carpes, A. C. B. M. de Oca, M. A. G. dos Santos, C. C. Santana, C. R. D. Correia, J. Org. Chem. 2005, 70, 1050-1053, and references therein;
-
-
-
-
46
-
-
0037032313
-
-
d) D. M. Barnes, J. Ji, M. G. Fickes, M. A. Fitzgerald, S. A. King, H. E. Morton, F. A. Plagge, M. Preskill, S. H. Wagaw, S. J. Wittenberger, J. Zhang, J. Am. Chem. Soc. 2002, 124, 13097-13105;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 13097-13105
-
-
Barnes, D.M.1
Ji, J.2
Fickes, M.G.3
Fitzgerald, M.A.4
King, S.A.5
Morton, H.E.6
Plagge, F.A.7
Preskill, M.8
Wagaw, S.H.9
Wittenberger, S.J.10
Zhang, J.11
-
47
-
-
0000188529
-
-
e) J. Mulzer, R. Zuhse, R. Schmiechen, Angew. Chem. 1992, 104, 914-915;
-
(1992)
Angew. Chem
, vol.104
, pp. 914-915
-
-
Mulzer, J.1
Zuhse, R.2
Schmiechen, R.3
|