-
1
-
-
0028950654
-
-
For natural products that possess 3-substituted 3-hydroxy-oxindole substructures, see: a
-
For natural products that possess 3-substituted 3-hydroxy-oxindole substructures, see: a) Y. Kamano, H.-P. Zhang, Y. Ichihara, H. Kizu, K. Komiyama, G. R. Petit, Tetrahedron Lett. 1995, 36, 2783-2784;
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 2783-2784
-
-
Kamano, Y.1
Zhang, H.-P.2
Ichihara, Y.3
Kizu, H.4
Komiyama, K.5
Petit, G.R.6
-
2
-
-
0028904861
-
-
b) H.-P. Zhang, Y. Kamano, Y. Ichihara, H. Kizu, K. Komiyama, H. Itokawa, G. R. Pettit, Tetrahedron 1995, 51, 5523-5528;
-
(1995)
Tetrahedron
, vol.51
, pp. 5523-5528
-
-
Zhang, H.-P.1
Kamano, Y.2
Ichihara, Y.3
Kizu, H.4
Komiyama, K.5
Itokawa, H.6
Pettit, G.R.7
-
3
-
-
84988053641
-
-
c) W. Balk-Bindseil, E. Helmke, H. Weyland, H. Laatsch, Liebigs Ann. 1995, 1291-1294;
-
(1995)
Liebigs Ann
, pp. 1291-1294
-
-
Balk-Bindseil, W.1
Helmke, E.2
Weyland, H.3
Laatsch, H.4
-
4
-
-
0035132521
-
-
d) Y.-Q. Tang, I. Sattler, R. Thiericke, S. Grabley, Eur. J. Org. Chem. 2001, 261-267;
-
(2001)
Eur. J. Org. Chem
, pp. 261-267
-
-
Tang, Y.-Q.1
Sattler, I.2
Thiericke, R.3
Grabley, S.4
-
5
-
-
0001023632
-
-
e) K. A. Ubaidullaev, R. Shakirov, S. Y. Yunosov, Khim. Prir. Soedin. 1976, 12, 553-554;
-
(1976)
Khim. Prir. Soedin
, vol.12
, pp. 553-554
-
-
Ubaidullaev, K.A.1
Shakirov, R.2
Yunosov, S.Y.3
-
7
-
-
0001525005
-
-
g) K. Monde, K. Sasaki, A. Shirata, M. Takasugi, Phytochemistry 1991, 30, 2915-2917;
-
(1991)
Phytochemistry
, vol.30
, pp. 2915-2917
-
-
Monde, K.1
Sasaki, K.2
Shirata, A.3
Takasugi, M.4
-
8
-
-
0034354468
-
-
h) K. Monde, S. Osawa, N. Harada, M. Takasugi, M. Suchy, P. Kutschy, M. Dzurilla, E. Balentova, Chem. Lett. 2000, 886-887;
-
(2000)
Chem. Lett
, pp. 886-887
-
-
Monde, K.1
Osawa, S.2
Harada, N.3
Takasugi, M.4
Suchy, M.5
Kutschy, P.6
Dzurilla, M.7
Balentova, E.8
-
9
-
-
0038644197
-
-
i) K. Monde, T. Taniguchi, N. Miura, S.-I. Nishimura, N. Harada, R. K. Dukor, L. A. Nafie, Tetrahedron Lett. 2003, 44, 6017-6020;
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 6017-6020
-
-
Monde, K.1
Taniguchi, T.2
Miura, N.3
Nishimura, S.-I.4
Harada, N.5
Dukor, R.K.6
Nafie, L.A.7
-
10
-
-
1342281639
-
-
j) H. Suzuki, H. Morita, M. Shiro, J.-I. Kobayashi, Tetrahedron 2004, 60, 2489-2495;
-
(2004)
Tetrahedron
, vol.60
, pp. 2489-2495
-
-
Suzuki, H.1
Morita, H.2
Shiro, M.3
Kobayashi, J.-I.4
-
11
-
-
0035905004
-
-
k) A. Fréchard, N. Fabre, C. Péan, S. Montaut, M.-T. Fauvel, P. Rollin, I. Fourasté, Tetrahedron Lett. 2001, 42, 9015-9017;
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 9015-9017
-
-
Fréchard, A.1
Fabre, N.2
Péan, C.3
Montaut, S.4
Fauvel, M.-T.5
Rollin, P.6
Fourasté, I.7
-
12
-
-
0034712160
-
-
l) J. Kohno, Y. Koguchi, M. Nishio, K. Nakao, M. Kuroda, R. Shimizu, T. Ohnuki, S. Komatsubara, J. Org. Chem. 2000, 65, 990-995.
-
(2000)
J. Org. Chem
, vol.65
, pp. 990-995
-
-
Kohno, J.1
Koguchi, Y.2
Nishio, M.3
Nakao, K.4
Kuroda, M.5
Shimizu, R.6
Ohnuki, T.7
Komatsubara, S.8
-
13
-
-
24144493658
-
-
For enantioselective catalytic aldol addition to isatins, see: a
-
For enantioselective catalytic aldol addition to isatins, see: a) G. Luppi, P. G Cozzi, M. Monari, B. Kaptein, Q. B. Broxterman, C. Tomasini, J. Org. Chem. 2005, 70, 7418-7421;
-
(2005)
J. Org. Chem
, vol.70
, pp. 7418-7421
-
-
Luppi, G.1
Cozzi, P.G.2
Monari, M.3
Kaptein, B.4
Broxterman, Q.B.5
Tomasini, C.6
-
14
-
-
33846467147
-
-
b) G Chen, Y. Wang, H. He, S. Gao, X. Yang, X. Hao, Heterocycles 2006, 68, 2327-2333;
-
(2006)
Heterocycles
, vol.68
, pp. 2327-2333
-
-
Chen, G.1
Wang, Y.2
He, H.3
Gao, S.4
Yang, X.5
Hao, X.6
-
15
-
-
33751290436
-
-
c) G Luppi, M. Monari, R. J. Corrêa, F. A. Violante, A. C. Pinto, B. Kaptein, Q. B. Broxterman, S. J. Garden, C. Tomasini, Tetrahedron 2006, 62, 12017-12024;
-
(2006)
Tetrahedron
, vol.62
, pp. 12017-12024
-
-
Luppi, G.1
Monari, M.2
Corrêa, R.J.3
Violante, F.A.4
Pinto, A.C.5
Kaptein, B.6
Broxterman, Q.B.7
Garden, S.J.8
Tomasini, C.9
-
16
-
-
38349176362
-
-
d) A. V. Malkov, M. A. Kabeshov, M. Bella, O. Kysilka, D. A. Malyshev, K. Pluháčková, P. Kočovskŷ, Org. Lett. 2007, 9, 5473-5476;
-
(2007)
Org. Lett
, vol.9
, pp. 5473-5476
-
-
Malkov, A.V.1
Kabeshov, M.A.2
Bella, M.3
Kysilka, O.4
Malyshev, D.A.5
Pluháčková, K.6
Kočovskŷ, P.7
-
17
-
-
34548310448
-
-
e) J.-R. Chen, X.-P. Liu, X.-Y Zhu, L. Liang, Y.-F. Qiao, J.-M. Zhang, W.-J. Xiao, Tetrahedron 2007, 63, 10437-10444;
-
(2007)
Tetrahedron
, vol.63
, pp. 10437-10444
-
-
Chen, J.-R.1
Liu, X.-P.2
Zhu, X.-Y.3
Liang, L.4
Qiao, Y.-F.5
Zhang, J.-M.6
Xiao, W.-J.7
-
18
-
-
38949114233
-
-
f) R. J. Corrêa, S. J. Garden, G. Angelici, C. Tomasini, Eur. J. Org. Chem. 2008, 736-744;
-
(2008)
Eur. J. Org. Chem
, pp. 736-744
-
-
Corrêa, R.J.1
Garden, S.J.2
Angelici, G.3
Tomasini, C.4
-
19
-
-
53849114724
-
-
g) S. Nakamura, N. Hara, H. Nakashima, K. Kubo, N. Shibata, T. Toru, Chem. Eur. J. 2008, 14, 8079-8081.
-
(2008)
Chem. Eur. J
, vol.14
, pp. 8079-8081
-
-
Nakamura, S.1
Hara, N.2
Nakashima, H.3
Kubo, K.4
Shibata, N.5
Toru, T.6
-
20
-
-
33746147475
-
-
For enantioselective catalytic addition of arylboronic acids to isatins, see: a
-
For enantioselective catalytic addition of arylboronic acids to isatins, see: a) P. Y. Toullec, R. B. C. Jagt, J. G. de Vries, B. L. Feringa, A. L. Minnaard, Org. Lett. 2006, 8, 2715-2718;
-
(2006)
Org. Lett
, vol.8
, pp. 2715-2718
-
-
Toullec, P.Y.1
Jagt, R.B.C.2
de Vries, J.G.3
Feringa, B.L.4
Minnaard, A.L.5
-
21
-
-
33748667844
-
-
b) R. Shintani, M. Inoue, T. Hayashi, Angew. Chem. 2006, 118, 3431-3434;
-
(2006)
Angew. Chem
, vol.118
, pp. 3431-3434
-
-
Shintani, R.1
Inoue, M.2
Hayashi, T.3
-
22
-
-
33746112742
-
-
Angew. Chem. Int. Ed. 2006, 45, 3353-3356;
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 3353-3356
-
-
-
23
-
-
58149279460
-
-
c) H. Lai, Z. Huang, Q. Wu, Y. Qin, J. Org. Chem. 2009, 74, 283-288.
-
(2009)
J. Org. Chem
, vol.74
, pp. 283-288
-
-
Lai, H.1
Huang, Z.2
Wu, Q.3
Qin, Y.4
-
24
-
-
0030997203
-
-
For enantioselective catalytic hydrogénation of isatins, see
-
For enantioselective catalytic hydrogénation of isatins, see: J.-F. Carpentier, A. Morteux, Tetrahedron: Asymmetry 1997, 8, 1083-1099.
-
(1997)
Tetrahedron: Asymmetry
, vol.8
, pp. 1083-1099
-
-
Carpentier, J.-F.1
Morteux, A.2
-
25
-
-
5344225888
-
-
For enantioselective catalytic addition of organozinc reagents to isatins, see: a
-
For enantioselective catalytic addition of organozinc reagents to isatins, see: a) K. Funabashi, M. Jachmann, M. Kanai, M. Shibasaki, Angew. Chem. 2003, 115, 5647-5650;
-
(2003)
Angew. Chem
, vol.115
, pp. 5647-5650
-
-
Funabashi, K.1
Jachmann, M.2
Kanai, M.3
Shibasaki, M.4
-
26
-
-
0344845086
-
-
Angew. Chem. Int. Ed. 2003, 42, 5489-5492.
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 5489-5492
-
-
-
27
-
-
33645756584
-
-
For enantioselective catalytic allylation of organozinc reagents to isatins, see
-
For enantioselective catalytic allylation of organozinc reagents to isatins, see: M. Kitajima, I. Mori, K. Arai, N. Kogure, H. Takayama, Tetrahedron Lett. 2006, 47, 3199-3202.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 3199-3202
-
-
Kitajima, M.1
Mori, I.2
Arai, K.3
Kogure, N.4
Takayama, H.5
-
28
-
-
33846995439
-
-
For selected reviews of C-C bond-forming hydrogénation and transfer hydrogénation methods, see: a
-
For selected reviews of C-C bond-forming hydrogénation and transfer hydrogénation methods, see: a) M.-Y Ngai, J.-R. Kong, M. J. Krische, J. Org. Chem. 2007, 72, 1063-1072;
-
(2007)
J. Org. Chem
, vol.72
, pp. 1063-1072
-
-
Ngai, M.-Y.1
Kong, J.-R.2
Krische, M.J.3
-
30
-
-
38049062493
-
-
c) E. Skucas, M.-Y Ngai, V. Komanduri, M. J. Krische, Acc. Chem. Res. 2007, 40, 1394-1401;
-
(2007)
Acc. Chem. Res
, vol.40
, pp. 1394-1401
-
-
Skucas, E.1
Ngai, M.-Y.2
Komanduri, V.3
Krische, M.J.4
-
32
-
-
70349953113
-
-
e) J. F Bower, I.S. Kim, R. L. Patman, M. J. Krische, Angew. Chem. 2009, 121, 36-48;
-
(2009)
Angew. Chem
, vol.121
, pp. 36-48
-
-
Bower, J.F.1
Kim, I.S.2
Patman, R.L.3
Krische, M.J.4
-
34
-
-
1842788947
-
-
For carbonyl and imine vinylation employing 1,3-enynes and 1,3-diynes as vinyl donors under hydrogenation conditions, see: a
-
For carbonyl and imine vinylation employing 1,3-enynes and 1,3-diynes as vinyl donors under hydrogenation conditions, see: a) H.-Y Jang, R. R. Huddleston, M. J. Krische, J. Am. Chem. Soc. 2004, 126, 4664-4665;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 4664-4665
-
-
Jang, H.-Y.1
Huddleston, R.R.2
Krische, M.J.3
-
35
-
-
23844494674
-
-
b) J.-R. Kong, C.-W. Cho, M. J. Krische, J. Am. Chem. Soc. 2005, 127, 11269-11276;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 11269-11276
-
-
Kong, J.-R.1
Cho, C.-W.2
Krische, M.J.3
-
36
-
-
31444453628
-
-
c) J.-R. Kong, M.-Y Ngai, M. J. Krische, J. Am. Chem. Soc. 2006, 128, 718-719;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 718-719
-
-
Kong, J.-R.1
Ngai, M.-Y.2
Krische, M.J.3
-
38
-
-
34848878354
-
-
e) Y.-T Hong, C.-W. Cho, E. Skucas, M. J. Krische, Org. Lett. 2007, 9, 3745-3748;
-
(2007)
Org. Lett
, vol.9
, pp. 3745-3748
-
-
Hong, Y.-T.1
Cho, C.-W.2
Skucas, E.3
Krische, M.J.4
-
40
-
-
33747806634
-
-
For carbonyl and imine vinylation employing nonconjugated alkynes as vinyl donors under hydrogénation and transfer-hydrogenation conditions, see: a J.-U. Rhee, M. J. Krische, J. Am. Chem. Soc. 2006, 128, 10674-10675;
-
For carbonyl and imine vinylation employing nonconjugated alkynes as vinyl donors under hydrogénation and transfer-hydrogenation conditions, see: a) J.-U. Rhee, M. J. Krische, J. Am. Chem. Soc. 2006, 128, 10674-10675;
-
-
-
-
42
-
-
33846250049
-
-
c) M.-Y. Ngai, A. Barchuk, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 280-281;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 280-281
-
-
Ngai, M.-Y.1
Barchuk, A.2
Krische, M.J.3
-
43
-
-
34250817603
-
-
d) E. Skucas, J.-R. Kong, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 7242-7243;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 7242-7243
-
-
Skucas, E.1
Kong, J.-R.2
Krische, M.J.3
-
44
-
-
34447529183
-
-
e) A. Barchuk, M.-Y. Ngai, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 8432-8433;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 8432-8433
-
-
Barchuk, A.1
Ngai, M.-Y.2
Krische, M.J.3
-
45
-
-
35548979533
-
-
f) M.-Y. Ngai, A. Barchuk, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 12644-12645;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 12644-12645
-
-
Ngai, M.-Y.1
Barchuk, A.2
Krische, M.J.3
-
46
-
-
55949087716
-
-
g) S. B. Han, J. R. Kong, M. J. Krische, Org. Lett. 2008, 10, 4133-4135;
-
(2008)
Org. Lett
, vol.10
, pp. 4133-4135
-
-
Han, S.B.1
Kong, J.R.2
Krische, M.J.3
-
47
-
-
67749135569
-
-
h) R. L. Patman, M. R. Chaulagain, V. M. Williams, M. J. Krische, J. Am. Chem. Soc. 2009, 131, 2066-2067.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 2066-2067
-
-
Patman, R.L.1
Chaulagain, M.R.2
Williams, V.M.3
Krische, M.J.4
-
48
-
-
70349956312
-
-
For a review of catalytic reductive aldol and Mannich additionsemploying gaseous hydrogen as a terminal reductant, see: S. B. Han, A. Hassan, M. J. Krische, Synthesis 2008, 2669-2679
-
For a review of catalytic reductive aldol and Mannich additionsemploying gaseous hydrogen as a terminal reductant, see: S. B. Han, A. Hassan, M. J. Krische, Synthesis 2008, 2669-2679.
-
-
-
-
49
-
-
70349940995
-
-
For olefin reductive hydroacylation employing anhydrides asacyl donors under hydrogénation conditions, see: a Y.-T. Hong, A. Barchuk, M. J. Krische, Angew. Chem. 2006, 118, 7039-7042;
-
For olefin reductive hydroacylation employing anhydrides asacyl donors under hydrogénation conditions, see: a) Y.-T. Hong, A. Barchuk, M. J. Krische, Angew. Chem. 2006, 118, 7039-7042;
-
-
-
-
50
-
-
33750488411
-
-
Angew. Chem. Int. Ed. 2006, 45, 6885-6888;
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 6885-6888
-
-
-
51
-
-
0001319755
-
-
b) K. Kokubo, M. Miura, M. Nomura, Organometallics 1995, 14, 4521-4524.
-
(1995)
Organometallics
, vol.14
, pp. 4521-4524
-
-
Kokubo, K.1
Miura, M.2
Nomura, M.3
-
52
-
-
35548993714
-
-
For carbonyl allylation employing alienes as allyl donors underhydrogénation and transfer-hydrogenation conditions, see: a E. Skucas, J. F Bower, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 12678-12679;
-
For carbonyl allylation employing alienes as allyl donors underhydrogénation and transfer-hydrogenation conditions, see: a) E. Skucas, J. F Bower, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 12678-12679;
-
-
-
-
53
-
-
37049007450
-
-
b) J. F Bower, E. Skucas, R. L. Patman, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 15134-15135;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 15134-15135
-
-
Bower, J.F.1
Skucas, E.2
Patman, R.L.3
Krische, M.J.4
-
54
-
-
51649085840
-
-
c) M.-Y. Ngai, E. Skucas, M. J. Krische, Org. Lett. 2008, 10, 2705-2708;
-
(2008)
Org. Lett
, vol.10
, pp. 2705-2708
-
-
Ngai, M.-Y.1
Skucas, E.2
Krische, M.J.3
-
55
-
-
67849092737
-
-
d) E. Skucas, J. R. Zbieg, M. J. Krische, J. Am. Chem. Soc. 2009, 131, 5054-5055;
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 5054-5055
-
-
Skucas, E.1
Zbieg, J.R.2
Krische, M.J.3
-
56
-
-
70149095459
-
-
e) S. B. Han, I. S. Kim, H. Han, M. J. Krische, J. Am. Chem. Soc. 2009, 131, 6916-6917.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 6916-6917
-
-
Han, S.B.1
Kim, I.S.2
Han, H.3
Krische, M.J.4
-
57
-
-
33750493702
-
-
For carbonyl allylation employing 1,3-dienes as allyl donorsunder hydrogénation and transfer-hydrogenation conditions, see: a
-
For carbonyl allylation employing 1,3-dienes as allyl donorsunder hydrogénation and transfer-hydrogenation conditions, see: a) H.-Y Jang, R. R. Huddleston, M. J. Krische, Angew. Chem. 2003, 115, 4208-4211;
-
(2003)
Angew. Chem
, vol.115
, pp. 4208-4211
-
-
Jang, H.-Y.1
Huddleston, R.R.2
Krische, M.J.3
-
58
-
-
0141649629
-
-
Angew. Chem. Int. Ed. 2003, 42, 4074-4077;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 4074-4077
-
-
-
59
-
-
43549090940
-
-
b) J.F Bower, R. L. Patman, M. J. Krische, Org. Lett. 2008, 10, 1033-1035;
-
(2008)
Org. Lett
, vol.10
, pp. 1033-1035
-
-
Bower, J.F.1
Patman, R.L.2
Krische, M.J.3
-
60
-
-
43949117421
-
-
c) F Shibahara, J. F Bower, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 6338-6339;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 6338-6339
-
-
Shibahara, F.1
Bower, J.F.2
Krische, M.J.3
-
61
-
-
54849406161
-
-
d) FShibahara, J. F Bower, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 14120-14122.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 14120-14122
-
-
FShibahara, J.1
Bower, F.2
Krische, M.J.3
-
62
-
-
43949139260
-
-
For carbonyl allylation employing allylic acetates as allyl donorsunder transfer-hydrogenation conditions, see: a I. S. Kim, M.-Y. Ngai, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 6340-6341;
-
For carbonyl allylation employing allylic acetates as allyl donorsunder transfer-hydrogenation conditions, see: a) I. S. Kim, M.-Y. Ngai, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 6340-6341;
-
-
-
-
63
-
-
55549119981
-
-
b) I. S. Kim, M.-Y Ngai, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 14891-14899;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 14891-14899
-
-
Kim, I.S.1
Ngai, M.-Y.2
Krische, M.J.3
-
64
-
-
67749093229
-
-
c) I. S. Kim, S. B. Han, M. J. Krische, J. Am. Chem. Soc. 2009, 131, 2514-2520.
-
(2009)
J. Am. Chem. Soc
, vol.131
, pp. 2514-2520
-
-
Kim, I.S.1
Han, S.B.2
Krische, M.J.3
-
65
-
-
58249094810
-
-
For carbonyl propargylation employing 1,3-enynes as propargyldonors under transfer-hydrogenation conditions, see
-
For carbonyl propargylation employing 1,3-enynes as propargyldonors under transfer-hydrogenation conditions, see: R. L. Patman, V. M. Williams, J. F Bower, M. J. Krische, Angew. Chem. 2008, 120, 5298-5301;
-
(2008)
Angew. Chem
, vol.120
, pp. 5298-5301
-
-
Patman, R.L.1
Williams, V.M.2
Bower, J.F.3
Krische, M.J.4
-
66
-
-
48149091798
-
-
Angew. Chem. Int. Ed. 2008, 47, 5220-5223.
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 5220-5223
-
-
-
67
-
-
0001525348
-
-
For selected reviews on conventional enantioselective carbonylallylation, crotylation, and prenylation employing stoichiometricorganometallic reagents, see: a
-
For selected reviews on conventional enantioselective carbonylallylation, crotylation, and prenylation employing stoichiometricorganometallic reagents, see: a) R. W. Hoffmann, Angew. Chem. 1982, 94, 569-580;
-
(1982)
Angew. Chem
, vol.94
, pp. 569-580
-
-
Hoffmann, R.W.1
-
72
-
-
0142245730
-
-
Angew. Chem. Int. Ed. 2003, 42, 4732-4739;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 4732-4739
-
-
-
74
-
-
33646567165
-
-
f) C.-M. Yu, J. Youn, H.-K. Jung, Bull. Korean Chem. Soc. 2006, 27, 463-472;
-
(2006)
Bull. Korean Chem. Soc
, vol.27
, pp. 463-472
-
-
Yu, C.-M.1
Youn, J.2
Jung, H.-K.3
-
76
-
-
34447549207
-
-
h) D. G. Hall, Synlett 2007, 1644-1655.
-
(2007)
Synlett
, pp. 1644-1655
-
-
Hall, D.G.1
-
77
-
-
45249099537
-
-
For reviews encompassing catalytic asymmetric ketone addition, see: a
-
For reviews encompassing catalytic asymmetric ketone addition, see: a) M. Hatano, K. Ishihara, Synthesis 2008, 1647-1675;
-
(2008)
Synthesis
, pp. 1647-1675
-
-
Hatano, M.1
Ishihara, K.2
-
83
-
-
0347131100
-
-
Angew. Chem. Int. Ed. 2004, 43, 284-287.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 284-287
-
-
-
84
-
-
33749514608
-
-
For selected examples of catalytic enantioselective ketoneallylation, see: a
-
For selected examples of catalytic enantioselective ketoneallylation, see: a) Allylboration: S. Lou, P. N. Moquist, S. E. Schaus, J. Am. Chem. Soc. 2006, 128, 12660-12661;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 12660-12661
-
-
Allylboration, S.1
Lou, P.N.2
Moquist, S.E.S.3
-
85
-
-
3242808098
-
-
b) R. Wada, K. Oisaki, M. Kanai, M. Shibasaki, J. Am. Chem. Soc. 2004, 126, 8910-8911;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 8910-8911
-
-
Wada, R.1
Oisaki, K.2
Kanai, M.3
Shibasaki, M.4
-
87
-
-
4644248174
-
-
d) Allylstannation: J. G Kim, K. M. Waltz, D. Kwiatkowski, P. J. Walsh, J. Am. Chem. Soc. 2004, 126, 12580-12585;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 12580-12585
-
-
Allylstannation, J.1
Kim, G.2
Waltz, K.M.3
Kwiatkowski, D.4
Walsh, P.J.5
-
88
-
-
0000946629
-
-
e) S. Casolari, D. D'Ad-dario, E. Tagliavini, Org. Lett. 1999, 1, 1061-1063.
-
(1999)
Org. Lett
, vol.1
, pp. 1061-1063
-
-
Casolari, S.1
D'Ad-dario, D.2
Tagliavini, E.3
|