-
2
-
-
0026418434
-
-
B. M. Trost, Science 1991, 254, 1471-1477
-
(1991)
Science
, vol.254
, pp. 1471-1477
-
-
Trost, B.M.1
-
5
-
-
38949138457
-
-
P. A. Wender, V. A. Verma, T. J. Paxton, T. H. Pillow, Acc. Chem. Res. 2008, 41, 40-49
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 40-49
-
-
Wender, P.A.1
Verma, V.A.2
Paxton, T.J.3
Pillow, T.H.4
-
8
-
-
0002466970
-
-
in, (Ed.: T. Hudlicky) JAI, Greenwich, p .
-
P. A. Wender, B. L Miller, in Organic Synthesis: Theory and Applications, (Ed.:, T. Hudlicky,) JAI, Greenwich, 1993, p 27.
-
(1993)
Organic Synthesis: Theory and Applications
, pp. 27
-
-
Wender, P.A.1
Miller, B.L.2
-
9
-
-
80052020314
-
-
For selected reviews on cycloisomerization reactions, see
-
For selected reviews on cycloisomerization reactions, see
-
-
-
-
10
-
-
0036522941
-
-
C. Aubert, O. Buisine, M. Malacria, Chem. Rev. 2002, 102, 813-834
-
(2002)
Chem. Rev.
, vol.102
, pp. 813-834
-
-
Aubert, C.1
Buisine, O.2
Malacria, M.3
-
11
-
-
0035385137
-
-
B. M. Trost, D. F. Toste, A. B. Pinkerton, Chem. Rev. 2001, 101, 2067-2096
-
(2001)
Chem. Rev.
, vol.101
, pp. 2067-2096
-
-
Trost, B.M.1
Toste, D.F.2
Pinkerton, A.B.3
-
14
-
-
46649098072
-
-
Angew. Chem. Int. Ed. 2008, 47, 4268-4315.
-
(2008)
Angew. Chem. Int. Ed.
, vol.47
, pp. 4268-4315
-
-
-
15
-
-
80051974321
-
-
For selected examples of platinum-catalyzed cycloisomerization of nitrogen-tethered 1,6-enynes, see
-
For selected examples of platinum-catalyzed cycloisomerization of nitrogen-tethered 1,6-enynes, see
-
-
-
-
16
-
-
33751155795
-
-
J. Blum, H. Beer-Kraft, Y. Badrieh, J. Org. Chem. 1995, 60, 5567-5569
-
(1995)
J. Org. Chem.
, vol.60
, pp. 5567-5569
-
-
Blum, J.1
Beer-Kraft, H.2
Badrieh, Y.3
-
17
-
-
0001525502
-
-
N. Chatani, N. Furukawa, H. Sakurai, S. Murai, Organometallics 1996, 15, 901-903
-
(1996)
Organometallics
, vol.15
, pp. 901-903
-
-
Chatani, N.1
Furukawa, N.2
Sakurai, H.3
Murai, S.4
-
18
-
-
0032569211
-
-
A. Fürstner, H. Szillat, B. Gabor, R. Mynott, J. Am. Chem. Soc. 1998, 120, 8305-8314
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 8305-8314
-
-
Fürstner, A.1
Szillat, H.2
Gabor, B.3
Mynott, R.4
-
19
-
-
66149149009
-
-
D. Brissy, M. Skander, H. Jullien, P. Retailleau, A. Marinetti, Org. Lett. 2009, 11, 2137-2139
-
(2009)
Org. Lett.
, vol.11
, pp. 2137-2139
-
-
Brissy, D.1
Skander, M.2
Jullien, H.3
Retailleau, P.4
Marinetti, A.5
-
20
-
-
0035814401
-
-
A. Fürstner, F. Stelzer, H. Szillat, J. Am. Chem. Soc. 2001, 123, 11863-11869
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 11863-11869
-
-
Fürstner, A.1
Stelzer, F.2
Szillat, H.3
-
21
-
-
0035980290
-
-
For gold-catalyzed cycloisomerizations of homopropargylic diols, see
-
M. Méndez, M. Paz Munoz, C. Nevado, D. J. Cardenas, A. M. Echavarren, J. Am. Chem. Soc. 2001, 123, 10511-10520. For gold-catalyzed cycloisomerizations of homopropargylic diols, see
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 10511-10520
-
-
Méndez, M.1
Munoz, M.P.2
Nevado, C.3
Cardenas, D.J.4
Echavarren, A.M.5
-
22
-
-
22244492360
-
-
For selected studies on Au-catalyzed cycloisomerization of oxygen- and nitrogen-containing 1,6-enynes, see
-
S. Antoniotti, E. Genin, V. Michelet, J.-P. Genêt, J. Am. Chem. Soc. 2005, 127, 9976-9977. For selected studies on Au-catalyzed cycloisomerization of oxygen- and nitrogen-containing 1,6-enynes, see
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 9976-9977
-
-
Antoniotti, S.1
Genin, E.2
Michelet, V.3
Genêt, J.-P.4
-
23
-
-
79955551099
-
-
P. Perez-Galan, E. Herrero-Gomez, D. T. Hog, N. J. A. Martin, F. Maseras, A. M. Echavarren, Chem. Sci. 2011, 2, 141-149
-
(2011)
Chem. Sci.
, vol.2
, pp. 141-149
-
-
Perez-Galan, P.1
Herrero-Gomez, E.2
Hog, D.T.3
Martin, N.J.A.4
Maseras, F.5
Echavarren, A.M.6
-
24
-
-
72849107985
-
-
C.-M. Chao, D. Beltrami, P. Y. Toullec, V. Michelet, Chem. Commun. 2009, 6988-6990
-
(2009)
Chem. Commun.
, pp. 6988-6990
-
-
Chao, C.-M.1
Beltrami, D.2
Toullec, P.Y.3
Michelet, V.4
-
25
-
-
77953175284
-
-
Y. T. Lee, Y. K. Kang, Y. K. Chung, J. Org. Chem. 2009, 74, 7922-7934
-
(2009)
J. Org. Chem.
, vol.74
, pp. 7922-7934
-
-
Lee, Y.T.1
Kang, Y.K.2
Chung, Y.K.3
-
26
-
-
33748703833
-
-
S. I. Lee, S. M. Kim, S. Y. Kim, Y. K. Chung, Synlett 2006, 14, 2256-2260
-
(2006)
Synlett
, vol.14
, pp. 2256-2260
-
-
Lee, S.I.1
Kim, S.M.2
Kim, S.Y.3
Chung, Y.K.4
-
27
-
-
4344653148
-
-
C. Nieto-Oberhuber, M. P. Munoz, E. Bunuel, C. Nevado, D. J. Cardenas, A. M. Echavarren, Angew. Chem. 2004, 116, 2456-2460
-
(2004)
Angew. Chem.
, vol.116
, pp. 2456-2460
-
-
Nieto-Oberhuber, C.1
Munoz, M.P.2
Bunuel, E.3
Nevado, C.4
Cardenas, D.J.5
Echavarren, A.M.6
-
28
-
-
3242741475
-
-
Angew. Chem. Int. Ed. 2004, 43, 2402-2406. For representative examples of Rh-catalyzed skeletal rearrangements of 1,6-enynes, see
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 2402-2406
-
-
-
30
-
-
70350660550
-
-
K. Ota, S. I. Lee, J.-M. Tang, M. Takachi, H. Nakai, T. Morimoto, H. Sakurai, K. Kataoka, N. Chatani, J. Am. Chem. Soc. 2009, 131, 15203-15211
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 15203-15211
-
-
Ota, K.1
Lee, S.I.2
Tang, J.-M.3
Takachi, M.4
Nakai, H.5
Morimoto, T.6
Sakurai, H.7
Kataoka, K.8
Chatani, N.9
-
31
-
-
22944488016
-
-
For Ru- and W-catalyzed cycloisomerizations of bis-homopropargylic alcohols, see
-
H. Kim, C. Lee, J. Am. Chem. Soc. 2005, 127, 10180-10181. For Ru- and W-catalyzed cycloisomerizations of bis-homopropargylic alcohols, see
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 10180-10181
-
-
Kim, H.1
Lee, C.2
-
32
-
-
70749085501
-
-
A. Varela-Fernandez, C. Gonzalez-Rodriguez, J. A. Varela, L. Castedo, C. Saa, Org. Lett. 2009, 11, 5350-5353
-
(2009)
Org. Lett.
, vol.11
, pp. 5350-5353
-
-
Varela-Fernandez, A.1
Gonzalez-Rodriguez, C.2
Varela, J.A.3
Castedo, L.4
Saa, C.5
-
35
-
-
0034630891
-
-
F. E. McDonald, K. S. Reddy, Y. Diaz, J. Am. Chem. Soc. 2000, 122, 4304-4309
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 4304-4309
-
-
McDonald, F.E.1
Reddy, K.S.2
Diaz, Y.3
-
36
-
-
0030183224
-
-
For an example of ruthenium-catalyzed cycloisomerization of nitrogen-tethered 1,6-enynes, see
-
F. E. McDonald, J. L. Bowman, Tetrahedron Lett. 1996, 37, 4675-4678. For an example of ruthenium-catalyzed cycloisomerization of nitrogen-tethered 1,6-enynes, see
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 4675-4678
-
-
McDonald, F.E.1
Bowman, J.L.2
-
37
-
-
34248582574
-
-
For references on Ir(I)-catalyzed cycloisomerizations of 1,6-enynes, see
-
F. Monnier, C. Vovard-Le Bray, D. Castillo, V. Aubert, S. Derien, P. H. Dixneuf, L. Toupet, A. Ienco, C. Mealli, J. Am. Chem. Soc. 2007, 129, 6037-6049. For references on Ir(I)-catalyzed cycloisomerizations of 1,6-enynes, see
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 6037-6049
-
-
Monnier, F.1
Bray, C.V.-L.2
Castillo, D.3
Aubert, V.4
Derien, S.5
Dixneuf, P.H.6
Toupet, L.7
Ienco, A.8
Mealli, C.9
-
38
-
-
77953154393
-
-
J.-B. Xia, W.-B. Liu, T.-M. Wang, S.-L. You, Chem. Eur. J. 2010, 16, 6442-6446
-
(2010)
Chem. Eur. J.
, vol.16
, pp. 6442-6446
-
-
Xia, J.-B.1
Liu, W.-B.2
Wang, T.-M.3
You, S.-L.4
-
39
-
-
23944449251
-
-
T. Shibata, Y. Kobayashi, S. Maekawa, N. Toshida, K. Takagi, Tetrahedron 2005, 61, 9018-9024
-
(2005)
Tetrahedron
, vol.61
, pp. 9018-9024
-
-
Shibata, T.1
Kobayashi, Y.2
Maekawa, S.3
Toshida, N.4
Takagi, K.5
-
40
-
-
10844250034
-
-
T. Shibata, M. Yamasaki, S. Kadowaki, K. Takagi, Synlett 2004, 2812-2814
-
(2004)
Synlett
, pp. 2812-2814
-
-
Shibata, T.1
Yamasaki, M.2
Kadowaki, S.3
Takagi, K.4
-
41
-
-
0035874719
-
-
For iridium-catalyzed cycloisomerizations of homopropargylic diols, see
-
N. Chatani, H. Inoue, T. Morimoto, T. Muto, S. Murai, J. Org. Chem. 2001, 66, 4433-4436. For iridium-catalyzed cycloisomerizations of homopropargylic diols, see
-
(2001)
J. Org. Chem.
, vol.66
, pp. 4433-4436
-
-
Chatani, N.1
Inoue, H.2
Morimoto, T.3
Muto, T.4
Murai, S.5
-
42
-
-
33746320320
-
-
S. Antoniotti, E. Genin, V. Michelet, J. P. Genêt, Angew. Chem. 2005, 117, 5029-5033
-
(2005)
Angew. Chem.
, vol.117
, pp. 5029-5033
-
-
Antoniotti, S.1
Genin, E.2
Michelet, V.3
Genêt, J.P.4
-
43
-
-
23744466974
-
-
Angew. Chem. Int. Ed. 2005, 44, 4949-4953
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 4949-4953
-
-
-
45
-
-
77950817135
-
-
J. H. H. Ho, R. Hodgson, J. Wagler, B. A. Messerle, Dalton Trans. 2010, 39, 4062-4069
-
(2010)
Dalton Trans.
, vol.39
, pp. 4062-4069
-
-
Ho, J.H.H.1
Hodgson, R.2
Wagler, J.3
Messerle, B.A.4
-
46
-
-
58749101147
-
-
For gallium-catalyzed tandem cycloisomerizations/Friedel-Crafts additions, see
-
S. Selvaratnam, J. H. H. Ho, P. B. Huleatt, B. A. Messere, C. L. L. Chai, Tetrahedron Lett. 2009, 50, 1125-1127. For gallium-catalyzed tandem cycloisomerizations/Friedel-Crafts additions, see
-
(2009)
Tetrahedron Lett.
, vol.50
, pp. 1125-1127
-
-
Selvaratnam, S.1
Ho, J.H.H.2
Huleatt, P.B.3
Messere, B.A.4
Chai, C.L.L.5
-
47
-
-
78650403915
-
-
For silver-catalyzed cycloisomerization of homopropargylic diols, see
-
H.-J. Li, R. Guillot, V. Gandon, J. Org. Chem. 2010, 75, 8435-8449. For silver-catalyzed cycloisomerization of homopropargylic diols, see
-
(2010)
J. Org. Chem.
, vol.75
, pp. 8435-8449
-
-
Li, H.-J.1
Guillot, R.2
Gandon, V.3
-
48
-
-
34547957758
-
-
C. H. Oh, H. J. Yi, J. H. Lee, New J. Chem. 2007, 31, 835-837.
-
(2007)
New J. Chem.
, vol.31
, pp. 835-837
-
-
Oh, C.H.1
Yi, H.J.2
Lee, J.H.3
-
49
-
-
80051967921
-
-
For recent contributions of our group, see
-
For recent contributions of our group, see
-
-
-
-
51
-
-
58649119057
-
-
X. Moreau, A. Hours, L. Fensterbank, J.-P. Goddard, M. Malacria, S. Thorimbert, J. Organomet. Chem. 2009, 694, 561-565
-
(2009)
J. Organomet. Chem.
, vol.694
, pp. 561-565
-
-
Moreau, X.1
Hours, A.2
Fensterbank, L.3
Goddard, J.-P.4
Malacria, M.5
Thorimbert, S.6
-
52
-
-
67749084445
-
-
G. Lemière, V. Gandon, K. Cariou, A. Hours, T. Fukuyama, A. L. Dhimane, L. Fensterbank, M. Malacria, J. Am. Chem. Soc. 2009, 131, 2993-3006
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 2993-3006
-
-
Lemière, G.1
Gandon, V.2
Cariou, K.3
Hours, A.4
Fukuyama, T.5
Dhimane, A.L.6
Fensterbank, L.7
Malacria, M.8
-
53
-
-
68949102738
-
-
N. Marion, G. Lernière, A. Correa, C. Costabile, R. S. Ramõn, X. Moreau. P. de Frémont, R. Dahmane, A. Hours, D. lesage, J.-C. Tabet, J.-P. Goddard, V. Gandon, L. Cavallo, L. Fensterbank, M. Malacria, S. P. Nolan, Chem. Eur. J. 2009, 15, 3243-3260
-
(2009)
Chem. Eur. J.
, vol.15
, pp. 3243-3260
-
-
Marion, N.1
Lernière, G.2
Correa, A.3
Costabile, C.4
Ramõn, R.S.5
Frémont, X.6
Moreau, P.D.7
Dahmane, R.8
Hours, A.9
Lesage, D.10
Tabet, J.-C.11
Goddard, J.-P.12
Gandon, V.13
Cavallo, L.14
Fensterbank, L.15
Malacria, M.16
Nolan, S.P.17
-
54
-
-
75649110408
-
-
Y. Harrak, A. Simonneau, M. Malacria, V. Gandon, L. Fensterbank, Chem. Commun. 2010, 865-867
-
(2010)
Chem. Commun.
, pp. 865-867
-
-
Harrak, Y.1
Simonneau, A.2
Malacria, M.3
Gandon, V.4
Fensterbank, L.5
-
55
-
-
77957132206
-
-
E. Benedetti, G. Lemière, L.-L. Chapellet, A. Penoni, G. Palmisano, M. Malacria, J.-P. Goddard, L. Fensterbank, Org. Lett. 2010, 12, 4396-4399.
-
(2010)
Org. Lett.
, vol.12
, pp. 4396-4399
-
-
Benedetti, E.1
Lemière, G.2
Chapellet, L.-L.3
Penoni, A.4
Palmisano, G.5
Malacria, M.6
Goddard, J.-P.7
Fensterbank, L.8
-
56
-
-
80051963453
-
-
2
-
2, see
-
-
-
-
57
-
-
53849132291
-
-
X. Wu, J. Liu, X. Li, A. Zanotti-Gerosa, F. Hancock, D. Vinci, J. Ruan, J. Xiao, Angew. Chem. 2006, 118, 6870-6874
-
(2006)
Angew. Chem.
, vol.118
, pp. 6870-6874
-
-
Wu, X.1
Liu, J.2
Li, X.3
Zanotti-Gerosa, A.4
Hancock, F.5
Vinci, D.6
Ruan, J.7
Xiao, J.8
-
58
-
-
33750193289
-
-
Angew. Chem. Int. Ed. 2006, 45, 6718-6722
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 6718-6722
-
-
-
59
-
-
33947095560
-
-
V. S. Sridevi, W. Y. Fan, W. K. Leong, Organometallics 2007, 26, 1157-1160
-
(2007)
Organometallics
, vol.26
, pp. 1157-1160
-
-
Sridevi, V.S.1
Fan, W.Y.2
Leong, W.K.3
-
60
-
-
51949093660
-
-
L. Li, W. W. Brennessel, W. D. Jones, J. Am. Chem. Soc. 2008, 130, 12414-12419
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 12414-12419
-
-
Li, L.1
Brennessel, W.W.2
Jones, W.D.3
-
61
-
-
0001334479
-
-
K. Fujita, K. Yamamoto, R. Yamaguchi, Org. Lett. 2002, 4, 2691-2694
-
(2002)
Org. Lett.
, vol.4
, pp. 2691-2694
-
-
Fujita, K.1
Yamamoto, K.2
Yamaguchi, R.3
-
62
-
-
38749127622
-
-
R. Yamaguchi, S. Kawagoe, C. Asai, K. Fujita, Org. Lett. 2008, 10, 181-184
-
(2008)
Org. Lett.
, vol.10
, pp. 181-184
-
-
Yamaguchi, R.1
Kawagoe, S.2
Asai, C.3
Fujita, K.4
-
63
-
-
33846406900
-
-
N. A. Owston, A. J. Parker, J. M. J. Williams, Org. Lett. 2007, 9, 73-75
-
(2007)
Org. Lett.
, vol.9
, pp. 73-75
-
-
Owston, N.A.1
Parker, A.J.2
Williams, J.M.J.3
-
64
-
-
79951915891
-
-
For recent examples of Ir[III]-catalyzed reaction, see
-
Y.-F. Han, H. Li, P. Hu, G.-X. Jin, Organometallics 2011, 30, 905-911. For recent examples of Ir[III]-catalyzed reaction, see
-
(2011)
Organometallics
, vol.30
, pp. 905-911
-
-
Han, Y.-F.1
Li, H.2
Hu, P.3
Jin, G.-X.4
-
65
-
-
80051989711
-
-
T. Vaidya, A. C. Atesin, I. R. Herrick, A. J. Frontier, R. Eisenberg, Angew. Chem. 2010, 122, 3435-3438
-
(2010)
Angew. Chem.
, vol.122
, pp. 3435-3438
-
-
Vaidya, T.1
Atesin, A.C.2
Herrick, I.R.3
Frontier, A.J.4
Eisenberg, R.5
-
66
-
-
77951682954
-
-
Angew. Chem. Int. Ed. 2010, 49, 3363-3366
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 3363-3366
-
-
-
67
-
-
77955811172
-
-
M. Ez-Zoubir, F. Le Boucher d'Herouville, J. A. Brown, V. Ratovelomanana-Vidal, V. Michelet, Chem. Commun. 2010, 46, 6332-6334.
-
(2010)
Chem. Commun.
, vol.46
, pp. 6332-6334
-
-
Ez-Zoubir, M.1
D'herouville, F.L.B.2
Brown, J.A.3
Ratovelomanana-Vidal, V.4
Michelet, V.5
-
68
-
-
80051954013
-
-
For the synthesis of bis-homopropargylic alcohols, see Supporting Information.
-
For the synthesis of bis-homopropargylic alcohols, see Supporting Information.
-
-
-
-
69
-
-
78649867052
-
-
E. Kumaran, V. S. Sridevi, W. K. Leong, Organometallics 2010, 29, 6417-6421
-
(2010)
Organometallics
, vol.29
, pp. 6417-6421
-
-
Kumaran, E.1
Sridevi, V.S.2
Leong, W.K.3
-
70
-
-
33947096523
-
-
V. S. Sridevi, W. Y. Fan, W. K. Leong, Organometallics 2007, 26, 1173-1177.
-
(2007)
Organometallics
, vol.26
, pp. 1173-1177
-
-
Sridevi, V.S.1
Fan, W.Y.2
Leong, W.K.3
-
71
-
-
80051958556
-
-
2 were employed to promote hydroalkoxylations without any significant modification of the reactivity. For technical details, see Supporting Information. Catalyses were also carried out with freshly prepared samples of iridium dimer.
-
2 were employed to promote hydroalkoxylations without any significant modification of the reactivity. For technical details, see Supporting Information. Catalyses were also carried out with freshly prepared samples of iridium dimer.
-
-
-
-
72
-
-
80052018058
-
-
For references on iridium(III)-vinylidene intermediates, see
-
For references on iridium(III)-vinylidene intermediates, see
-
-
-
-
73
-
-
80051981309
-
-
[8a]
-
[8a]
-
-
-
-
74
-
-
80051978526
-
-
[8b]. For selected studies on iridium(I)-vinylidene intermediates, see
-
[8b]. For selected studies on iridium(I)-vinylidene intermediates, see
-
-
-
-
75
-
-
0036230389
-
-
C. S. Chin, G. Won, D. Chong, M. Kim, H. Lee, Acc.Chem. Res. 2002, 35, 218-225
-
(2002)
Acc.Chem. Res.
, vol.35
, pp. 218-225
-
-
Chin, C.S.1
Won, G.2
Chong, D.3
Kim, M.4
Lee, H.5
-
76
-
-
0000501827
-
-
For a recent review on other metal-vinylidene intermediates, see
-
T. Ohmura, S. Yorozuya, Y. Yamamoto, N. Miyaura, Organometallics 2000, 19, 365-367. For a recent review on other metal-vinylidene intermediates, see
-
(2000)
Organometallics
, vol.19
, pp. 365-367
-
-
Ohmura, T.1
Yorozuya, S.2
Yamamoto, Y.3
Miyaura, N.4
-
78
-
-
80052017400
-
-
As suggested by one referee, because we are dealing with a dimeric precatalyst, gem-dimetalated species may be at work, see
-
As suggested by one referee, because we are dealing with a dimeric precatalyst, gem-dimetalated species may be at work, see
-
-
-
-
79
-
-
41549152977
-
-
P. H.-Y. Cheong, P. Morganelli, M. R. Luzung, K. N. Houk, F. D. Toste, J. Am. Chem. Soc. 2008, 130, 4517-4526
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 4517-4526
-
-
Cheong, P.H.-Y.1
Morganelli, P.2
Luzung, M.R.3
Houk, K.N.4
Toste, F.D.5
-
80
-
-
70350004081
-
-
D. Weber, M. A. Tarselli, M. R. Gagné, Angew. Chem. 2009, 121, 5843-5846
-
(2009)
Angew. Chem.
, vol.121
, pp. 5843-5846
-
-
Weber, D.1
Tarselli, M.A.2
Gagné, M.R.3
-
81
-
-
70349904871
-
-
Angew. Chem. Int. Ed. 2009, 48, 5733-5736
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 5733-5736
-
-
-
82
-
-
79952266862
-
-
G. Seidel, C. W. Lehmann, A. Fürstner, Angew. Chem. 2010, 122, 8644-8648
-
(2010)
Angew. Chem.
, vol.122
, pp. 8644-8648
-
-
Seidel, G.1
Lehmann, C.W.2
Fürstner, A.3
-
83
-
-
78149425384
-
-
Angew. Chem. Int. Ed. 2010, 49, 8466-8470.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 8466-8470
-
-
-
84
-
-
80052001130
-
-
To facilitate the nucleophilic attack, an intramolecular complexation of the OH group to the iridium(III) catalysts, could also be postulated, as already described for gold-catalyzed addition of alcohols to alkynes. See
-
To facilitate the nucleophilic attack, an intramolecular complexation of the OH group to the iridium(III) catalysts, could also be postulated, as already described for gold-catalyzed addition of alcohols to alkynes. See
-
-
-
-
85
-
-
80052010698
-
-
[4g]
-
[4g]
-
-
-
-
86
-
-
0001459366
-
-
J. H. Teles, S. Brode, M. Chabanas, Angew. Chem. 1998, 110, 1475-1478
-
(1998)
Angew. Chem.
, vol.110
, pp. 1475-1478
-
-
Teles, J.H.1
Brode, S.2
Chabanas, M.3
-
87
-
-
0032486218
-
-
For a computational study on the mechanism of iridium(I)-catalyzed double hydroalkoxylation, see
-
Angew. Chem. Int. Ed. 1998, 37, 1415-1418. For a computational study on the mechanism of iridium(I)-catalyzed double hydroalkoxylation, see
-
(1998)
Angew. Chem. Int. Ed.
, vol.37
, pp. 1415-1418
-
-
-
88
-
-
79751490580
-
-
T. Fjermestad, J. H. H. Ho, S. A. Macgregor, B. A. Messerle, D. Tuna, Organometallics 2011, 30, 618-626.
-
(2011)
Organometallics
, vol.30
, pp. 618-626
-
-
Fjermestad, T.1
Ho, J.H.H.2
MacGregor, S.A.3
Messerle, B.A.4
Tuna, D.5
-
89
-
-
80051987817
-
-
For the synthesis of nitrogen- and oxygen-tethered 1,6-enynes, see Supporting Information.
-
For the synthesis of nitrogen- and oxygen-tethered 1,6-enynes, see Supporting Information.
-
-
-
-
90
-
-
80051974654
-
-
The relative configuration of product 4g was deduced from NOE experiments. The configurations of 4c, 4d, 4i and 6a have been attributed by analogy with compound 4g.
-
The relative configuration of product 4g was deduced from NOE experiments. The configurations of 4c, 4d, 4i and 6a have been attributed by analogy with compound 4g.
-
-
-
-
91
-
-
80051960595
-
-
2 after 20 h in refluxing DCE
-
2 after 20 h in refluxing DCE.
-
-
-
-
93
-
-
33845247117
-
-
L. Zhang, J. Sun, S. A. Kozmin, Adv. Synth. Catal. 2006, 348, 2271-2296.
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 2271-2296
-
-
Zhang, L.1
Sun, J.2
Kozmin, S.A.3
|