-
3
-
-
0003942864
-
-
Wiley, NY
-
E. L. Eliel, S. H. Wilen, L. N. Mander, in Stereochemistry of Organic Compounds Wiley, NY, 1994, pp. 696-7.
-
(1994)
Stereochemistry of Organic Compounds
, pp. 696-697
-
-
Eliel, E.L.1
Wilen, S.H.2
Mander, L.N.3
-
4
-
-
37549039870
-
-
For strategic alkylations of cyclic nitriles, excluding oxonitriles, in total syntheses see: a
-
For strategic alkylations of cyclic nitriles, excluding oxonitriles, in total syntheses see: a) O. E. Hutt, L. N. Mander, J. Org. Chem. 2007, 72, 10130;
-
(2007)
J. Org. Chem
, vol.72
, pp. 10130
-
-
Hutt, O.E.1
Mander, L.N.2
-
7
-
-
0037128503
-
-
d) H. Miyaoka, H. Shida, N. Yamada, H. Mitome, N. Yamada, Tetrahedron Lett. 2003, 43, 2227;
-
(2003)
Tetrahedron Lett
, vol.43
, pp. 2227
-
-
Miyaoka, H.1
Shida, H.2
Yamada, N.3
Mitome, H.4
Yamada, N.5
-
8
-
-
18044399275
-
-
e) S. M. A. Rahman, H. Ohno, T. Murata, H. Yoshino, N. Satoh, K. Murakami, D. Patra, C. Iwata, N. Maezaki, T. Tanaka, Org. Lett. 2001, 3, 619;
-
(2001)
Org. Lett
, vol.3
, pp. 619
-
-
Rahman, S.M.A.1
Ohno, H.2
Murata, T.3
Yoshino, H.4
Satoh, N.5
Murakami, K.6
Patra, D.7
Iwata, C.8
Maezaki, N.9
Tanaka, T.10
-
9
-
-
0035854231
-
-
f) S. M. A. Rahman, H. Ohno, T. Murata, H. Yoshino, N. Satoh, K. Murakami, D. Patra, C. Iwata, N. Maezaki, T. Tanaka, J. Org. Chem. 2001, 66, 4831;
-
(2001)
J. Org. Chem
, vol.66
, pp. 4831
-
-
Rahman, S.M.A.1
Ohno, H.2
Murata, T.3
Yoshino, H.4
Satoh, N.5
Murakami, K.6
Patra, D.7
Iwata, C.8
Maezaki, N.9
Tanaka, T.10
-
10
-
-
0034632363
-
-
g) E. Piers, S. Caille, G. Chen, Org. Lett. 2000, 2, 2483;
-
(2000)
Org. Lett
, vol.2
, pp. 2483
-
-
Piers, E.1
Caille, S.2
Chen, G.3
-
11
-
-
37049082582
-
-
h) E. Piers, M. L. Breau, Y. Han, G. L. Plourde, W.-L. Yeh, J. Chem. Soc. Perkin Trans. 1 1995, 963;
-
(1995)
J. Chem. Soc. Perkin Trans. 1
, pp. 963
-
-
Piers, E.1
Breau, M.L.2
Han, Y.3
Plourde, G.L.4
Yeh, W.-L.5
-
13
-
-
0027495588
-
-
j) D. J. Kucera, S. J. O'Connor, L. E. Overman, J. Org. Chem. 1993, 58, 5304;
-
(1993)
J. Org. Chem
, vol.58
, pp. 5304
-
-
Kucera, D.J.1
O'Connor, S.J.2
Overman, L.E.3
-
15
-
-
0026341949
-
-
l) S. Darvesh, A. S. Grant, D. I. MaGee, Z. Valenta, Can. J. Chem. 1991, 69, 712;
-
(1991)
Can. J. Chem
, vol.69
, pp. 712
-
-
Darvesh, S.1
Grant, A.S.2
MaGee, D.I.3
Valenta, Z.4
-
16
-
-
0024917734
-
-
m) S. Darvesh, A. S. Grant, D. I. MaGee, Z. Valenta, Can. J. Chem. 1989, 67, 2237;
-
(1989)
Can. J. Chem
, vol.67
, pp. 2237
-
-
Darvesh, S.1
Grant, A.S.2
MaGee, D.I.3
Valenta, Z.4
-
17
-
-
0001070325
-
-
n) Z. Ahmad, P. Goswami, R. V. Venkateswaran, Tetrahedron 1989, 45, 6833;
-
(1989)
Tetrahedron
, vol.45
, pp. 6833
-
-
Ahmad, Z.1
Goswami, P.2
Venkateswaran, R.V.3
-
20
-
-
11044237354
-
-
q) Z. Ahmad, P. Goswami, R. V. Venkateswaran, Tetrahedron Lett. 1987, 28, 4329.
-
(1987)
Tetrahedron Lett
, vol.28
, pp. 4329
-
-
Ahmad, Z.1
Goswami, P.2
Venkateswaran, R.V.3
-
21
-
-
57349170471
-
-
D. S. Watt, S. Arseniyadis, K. S. Kyler, Org. React. 1984, 31, 1.
-
(1984)
Org. React
, vol.31
, pp. 1
-
-
Watt, D.S.1
Arseniyadis, S.2
Kyler, K.S.3
-
23
-
-
0008184347
-
-
b) F. Benedetti, F. Berti, S. Fabrissin, T. Gianferrara J. Org. Chem. 1994, 59, 1518.
-
(1994)
J. Org. Chem
, vol.59
, pp. 1518
-
-
Benedetti, F.1
Berti, F.2
Fabrissin, S.3
Gianferrara, T.4
-
24
-
-
0004255688
-
-
Comparative alkylations of sterically hindered nitriles, acids, and esters demonstrate the superior nucleophilicity of metallated nitriles: J.-A. MacPhee, J.-E. DuBois, Tetrahedron 1980, 36, 775.
-
Comparative alkylations of sterically hindered nitriles, acids, and esters demonstrate the superior nucleophilicity of metallated nitriles: J.-A. MacPhee, J.-E. DuBois, Tetrahedron 1980, 36, 775.
-
-
-
-
27
-
-
33947090861
-
-
b) S. K. Dayal, S. Ehrenson, R. W. Taft, J. Am. Chem. Soc. 1972, 94, 9113.
-
(1972)
J. Am. Chem. Soc
, vol.94
, pp. 9113
-
-
Dayal, S.K.1
Ehrenson, S.2
Taft, R.W.3
-
28
-
-
0000774224
-
-
a) Y. Kawakami, H. Hisada, Y. Yamashita, Tetrahedron Lett. 1985, 26, 5835;
-
(1985)
Tetrahedron Lett
, vol.26
, pp. 5835
-
-
Kawakami, Y.1
Hisada, H.2
Yamashita, Y.3
-
32
-
-
33750337500
-
-
a) F. F. Fleming, G. Wei, Z. Zhiyu, O. W. Steward, Org. Lett. 2006, 8, 4903;
-
(2006)
Org. Lett
, vol.8
, pp. 4903
-
-
Fleming, F.F.1
Wei, G.2
Zhiyu, Z.3
Steward, O.W.4
-
33
-
-
2842568219
-
-
b) D. Enders, J. Kirchhoff, P. Gerdes, D. Mannes, G. Raabe, J. Runsink, G. Boche, M. Marsch, H. Ahlbrecht, H. Sommer, Eur. J. Org. Chem. 1998, 63.
-
(1998)
Eur. J. Org. Chem
, pp. 63
-
-
Enders, D.1
Kirchhoff, J.2
Gerdes, P.3
Mannes, D.4
Raabe, G.5
Runsink, J.6
Boche, G.7
Marsch, M.8
Ahlbrecht, H.9
Sommer, H.10
-
34
-
-
0001018933
-
-
For a theoretical analysis of aggregates and transition states for deprotonation see
-
For a theoretical analysis of aggregates and transition states for deprotonation see: R. Koch, B. Wiedel, E. Anders, J. Org. Chem. 1996, 61, 2523.
-
(1996)
J. Org. Chem
, vol.61
, pp. 2523
-
-
Koch, R.1
Wiedel, B.2
Anders, E.3
-
37
-
-
0010929622
-
-
For a related dimeric ketenimine structure see
-
For a related dimeric ketenimine structure see: V. Y. Lee, H. Ranaivonjatovo, J. Escudié, J. Satgé, A. Dubourg, J.-P. Declercq, M. P. Egorov, O. M. Nefedov, Organometallics 1998, 17, 1517.
-
(1998)
Organometallics
, vol.17
, pp. 1517
-
-
Lee, V.Y.1
Ranaivonjatovo, H.2
Escudié, J.3
Satgé, J.4
Dubourg, A.5
Declercq, J.-P.6
Egorov, M.P.7
Nefedov, O.M.8
-
39
-
-
0034008787
-
-
a) Y. Tanabe, H. Seino, Y. Ishii, M. Hidai, J. Am. Chem. Soc. 2000, 122, 1690;
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 1690
-
-
Tanabe, Y.1
Seino, H.2
Ishii, Y.3
Hidai, M.4
-
40
-
-
0033915260
-
-
b) S.-I. Murahashi, K. Take, T. Naota, H. Takaya, Synlett 2000, 1016;
-
(2000)
Synlett
, pp. 1016
-
-
Murahashi, S.-I.1
Take, K.2
Naota, T.3
Takaya, H.4
-
41
-
-
0033556019
-
-
c) S. Triki, J. S. Pala, M. Decoster, P. Molinié, L. Toupet, Angew. Chem. Int. Ed. 1999, 38, 113;
-
(1999)
Angew. Chem. Int. Ed
, vol.38
, pp. 113
-
-
Triki, S.1
Pala, J.S.2
Decoster, M.3
Molinié, P.4
Toupet, L.5
-
42
-
-
33749093359
-
-
d) M. Hirano, A. Takenaka, Y. Mizuho, M. Hiraoka, S. Komiya, J. Chem. Soc., Dalton Trans. 1999, 3209;
-
(1999)
J. Chem. Soc., Dalton Trans
, pp. 3209
-
-
Hirano, M.1
Takenaka, A.2
Mizuho, Y.3
Hiraoka, M.4
Komiya, S.5
-
43
-
-
0001024204
-
-
e) M. L. Yates, A. M. Arif, J. L. Manson, B. A. Kalm, B. M. Burkhart, J. S. Miller, Inorg. Chem. 1998, 37, 840;
-
(1998)
Inorg. Chem
, vol.37
, pp. 840
-
-
Yates, M.L.1
Arif, A.M.2
Manson, J.L.3
Kalm, B.A.4
Burkhart, B.M.5
Miller, J.S.6
-
44
-
-
0005937022
-
-
f) L. Jäger, C. Tretner, H. Hartung, M. Biedermann, Chem. Ber./Recueil 1997, 130, 1007;
-
(1997)
Chem. Ber./Recueil
, vol.130
, pp. 1007
-
-
Jäger, L.1
Tretner, C.2
Hartung, H.3
Biedermann, M.4
-
45
-
-
0030455402
-
-
g) H. Zhao, R. A. Heintz, K. R. Dunbar, R. D. Rogers, J. Am. Chem. Soc. 1996, 118, 12844;
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 12844
-
-
Zhao, H.1
Heintz, R.A.2
Dunbar, K.R.3
Rogers, R.D.4
-
46
-
-
15844412400
-
-
h) S.-I. Murahashi, T. Naota, H. Taki, M. Mizuno, H. Takaya, S. Komiya, Y. Mizuho, N. Oyasato, M. Hiraoka, M. Hirano, A. Fukuoka, J. Am. Chem. Soc. 1995, 117, 12436;
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 12436
-
-
Murahashi, S.-I.1
Naota, T.2
Taki, H.3
Mizuno, M.4
Takaya, H.5
Komiya, S.6
Mizuho, Y.7
Oyasato, N.8
Hiraoka, M.9
Hirano, M.10
Fukuoka, A.11
-
47
-
-
0002190740
-
-
i) M. Hirano, Y. Ito, M. Hirai, A. Fukuoka, S. Komiya, Chem. Lett. 1993, 2057;
-
(1993)
Chem. Lett
, pp. 2057
-
-
Hirano, M.1
Ito, Y.2
Hirai, M.3
Fukuoka, A.4
Komiya, S.5
-
51
-
-
53849129261
-
-
a) T. Naota, A. Tannna, S. Kamuro, N. Hieda, K. Ogata, S.-I. Murahashi, H. Takaya, Chem. Eur. J. 2008, 14, 2482;
-
(2008)
Chem. Eur. J
, vol.14
, pp. 2482
-
-
Naota, T.1
Tannna, A.2
Kamuro, S.3
Hieda, N.4
Ogata, K.5
Murahashi, S.-I.6
Takaya, H.7
-
52
-
-
0037134866
-
-
b) T. Naota, A. Tannna, S. Kamuro, S.-I. Murahashi, J. Am. Chem. Soc. 2002, 124, 6842;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 6842
-
-
Naota, T.1
Tannna, A.2
Kamuro, S.3
Murahashi, S.-I.4
-
53
-
-
0034728564
-
-
c) T. Naota, A. Tannna, S.-I. Murahashi, J. Am. Chem. Soc. 2000, 122, 2960;
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 2960
-
-
Naota, T.1
Tannna, A.2
Murahashi, S.-I.3
-
54
-
-
0034651472
-
-
d) P. R. Alburquerque, A. R. Pinhas, J. A. Krause Bauer, Inorg. Chim. Acta 2000, 298, 239;
-
(2000)
Inorg. Chim. Acta
, vol.298
, pp. 239
-
-
Alburquerque, P.R.1
Pinhas, A.R.2
Krause Bauer, J.A.3
-
55
-
-
0000175562
-
-
e) J. Ruiz, V. Rodríguez, G. López, J. Casabó, E. Molins, C. Miravitlles, Organometallics 1999, 18, 1177;
-
(1999)
Organometallics
, vol.18
, pp. 1177
-
-
Ruiz, J.1
Rodríguez, V.2
López, G.3
Casabó, J.4
Molins, E.5
Miravitlles, C.6
-
56
-
-
0000632266
-
-
f) F. Ragaini, F. Porta, A. Fumagalli, F. Demartin, Organometallics 1991, 10, 3785;
-
(1991)
Organometallics
, vol.10
, pp. 3785
-
-
Ragaini, F.1
Porta, F.2
Fumagalli, A.3
Demartin, F.4
-
57
-
-
0000497665
-
-
g) F. Porta, F. Ragaini, S. Cenini, F. Demartin, Organometallics 1990, 9, 929;
-
(1990)
Organometallics
, vol.9
, pp. 929
-
-
Porta, F.1
Ragaini, F.2
Cenini, S.3
Demartin, F.4
-
58
-
-
0343969469
-
-
h) J. J. Ko, T. M. Bockman, J. K. Kochi, Organometallics 1990, 9, 1833;
-
(1990)
Organometallics
, vol.9
, pp. 1833
-
-
Ko, J.J.1
Bockman, T.M.2
Kochi, J.K.3
-
60
-
-
37049082898
-
-
j) S. K. Chopra, D. Cunningham, S. Kavanagh, P. McArdle, G. Moran, J. Chem. Soc., Dalton Trans. 1987, 2927;
-
(1987)
J. Chem. Soc., Dalton Trans
, pp. 2927
-
-
Chopra, S.K.1
Cunningham, D.2
Kavanagh, S.3
McArdle, P.4
Moran, G.5
-
61
-
-
37049099277
-
-
k) A. Del Pra, E. Forsellini, G. Bombieri, R. A. Michelin, R. Ros, J. Chem. Soc., Dalton Trans. 1979, 1862;
-
(1979)
J. Chem. Soc., Dalton Trans
, pp. 1862
-
-
Del Pra, A.1
Forsellini, E.2
Bombieri, G.3
Michelin, R.A.4
Ros, R.5
-
62
-
-
37049107708
-
-
l) M. Lenarda, N. B. Pahor, M. Calligaris, M. Graziani, L. Randaccio, J. Chem. Soc., Chem. Commun. 1978, 279;
-
(1978)
J. Chem. Soc., Chem. Commun
, pp. 279
-
-
Lenarda, M.1
Pahor, N.B.2
Calligaris, M.3
Graziani, M.4
Randaccio, L.5
-
63
-
-
0006426165
-
-
m) R. Schlodder, J. A. Ibers, M. Lenarda, M. Graziani, J. Am. Chem. Soc. 1974, 96, 6893;
-
(1974)
J. Am. Chem. Soc
, vol.96
, pp. 6893
-
-
Schlodder, R.1
Ibers, J.A.2
Lenarda, M.3
Graziani, M.4
-
64
-
-
0007882537
-
-
n) D. J. Yarrow, J. A. Ibers, M. Lenarda, M. Graziani, J. Organomet. Chem. 1974, 70, 133.
-
(1974)
J. Organomet. Chem
, vol.70
, pp. 133
-
-
Yarrow, D.J.1
Ibers, J.A.2
Lenarda, M.3
Graziani, M.4
-
66
-
-
18744411274
-
-
a) F. F. Fleming, S. Gudipati, Z. Zhang, W. Liu, O. W. Steward, J. Org. Chem. 2005, 70, 3845;
-
(2005)
J. Org. Chem
, vol.70
, pp. 3845
-
-
Fleming, F.F.1
Gudipati, S.2
Zhang, Z.3
Liu, W.4
Steward, O.W.5
-
67
-
-
15444369069
-
-
b) F. F. Fleming, Z. Zhang, W. Liu, P. Knochel, J. Org. Chem. 2005, 70, 2200;
-
(2005)
J. Org. Chem
, vol.70
, pp. 2200
-
-
Fleming, F.F.1
Zhang, Z.2
Liu, W.3
Knochel, P.4
-
68
-
-
0037054157
-
-
c) J. Thibonnet, V. A. Vu, P. Knochel, Tetrahedron 2002, 58, 4787;
-
(2002)
Tetrahedron
, vol.58
, pp. 4787
-
-
Thibonnet, J.1
Vu, V.A.2
Knochel, P.3
-
70
-
-
0035819619
-
-
K. A. Miller, T. W. Watson, J. E. Bender IV, M. M. B. Holl, J. W. Kamp, J. Am. Chem. Soc. 2001, 123, 982.
-
K. A. Miller, T. W. Watson, J. E. Bender IV, M. M. B. Holl, J. W. Kamp, J. Am. Chem. Soc. 2001, 123, 982.
-
-
-
-
77
-
-
84985520755
-
-
G. Boche, M. Marsch, K. Harms, Angew. Chem. Int. Ed. Engl. 1986, 25, 373.
-
(1986)
Angew. Chem. Int. Ed. Engl
, vol.25
, pp. 373
-
-
Boche, G.1
Marsch, M.2
Harms, K.3
-
78
-
-
33748236338
-
-
J. Baker, N. D. R. Barnett, D. Barr, W. Clegg, R. E. Mulvey, P. A. O'Neil, Angew. Chem. Int. Ed. Engl. 1993, 32, 1366.
-
(1993)
Angew. Chem. Int. Ed. Engl
, vol.32
, pp. 1366
-
-
Baker, J.1
Barnett, N.D.R.2
Barr, D.3
Clegg, W.4
Mulvey, R.E.5
O'Neil, P.A.6
-
79
-
-
0000609569
-
-
G. Boche, K. Harms, M. Marsch, J. Am. Chem. Soc. 1988, 110, 6925.
-
(1988)
J. Am. Chem. Soc
, vol.110
, pp. 6925
-
-
Boche, G.1
Harms, K.2
Marsch, M.3
-
80
-
-
0000576324
-
-
J.-Y. Le Questel, M. Berthelot, C. Laurence, J. Phys. Org. Chem. 2000, 13, 347.
-
(2000)
J. Phys. Org. Chem
, vol.13
, pp. 347
-
-
Le Questel, J.-Y.1
Berthelot, M.2
Laurence, C.3
-
81
-
-
0001686345
-
-
a) P. R. Carlier, B. L. Lucht, D. B. Collum, J. Am. Chem. Soc. 1994, 116, 11602;
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 11602
-
-
Carlier, P.R.1
Lucht, B.L.2
Collum, D.B.3
-
83
-
-
2542514849
-
-
R. Sott, J. Granander, G. Hilmersson, J. Am. Chem. Soc. 2004, 126, 6798.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 6798
-
-
Sott, R.1
Granander, J.2
Hilmersson, G.3
-
84
-
-
0035904251
-
-
For a related interconversion of palladium complexes see
-
For a related interconversion of palladium complexes see: M. Kujime, S. Hikichi, M. Akita, Organometallics 2001, 20, 4049.
-
(2001)
Organometallics
, vol.20
, pp. 4049
-
-
Kujime, M.1
Hikichi, S.2
Akita, M.3
-
85
-
-
0030529861
-
-
R. A. Michelin, M. Mozzon, R. Bertani, Coord. Chem. Rev. 1996, 147, 299.
-
(1996)
Coord. Chem. Rev
, vol.147
, pp. 299
-
-
Michelin, R.A.1
Mozzon, M.2
Bertani, R.3
-
88
-
-
0037827517
-
-
a) R. W. Hoffmann, M. Brönstrup, M. Muller, Org. Lett. 2003, 5, 313;
-
(2003)
Org. Lett
, vol.5
, pp. 313
-
-
Hoffmann, R.W.1
Brönstrup, M.2
Muller, M.3
-
89
-
-
0345451008
-
-
b) V. Schulze, M. Brönstrup, V. P. W. Böhm, P. Schwerdtfeger, M. Schimeczek, R. W. Hoffmann, Angew. Chem. Int. Ed. 1998, 37, 824;
-
(1998)
Angew. Chem. Int. Ed
, vol.37
, pp. 824
-
-
Schulze, V.1
Brönstrup, M.2
Böhm, V.P.W.3
Schwerdtfeger, P.4
Schimeczek, M.5
Hoffmann, R.W.6
-
90
-
-
84958308661
-
-
c) H. J. Reich, D. P. Green, N. H. Phillips, J. P. Borst, I. L. Reich, Phosphorus Sulfur Silicon 1992, 67, 83.
-
(1992)
Phosphorus Sulfur Silicon
, vol.67
, pp. 83
-
-
Reich, H.J.1
Green, D.P.2
Phillips, N.H.3
Borst, J.P.4
Reich, I.L.5
-
91
-
-
0037263577
-
-
For a computational analysis of lithiated cyclopropanecarbonitrile see
-
For a computational analysis of lithiated cyclopropanecarbonitrile see: P. R. Carlier, Chirality 2003, 15, 340.
-
(2003)
Chirality
, vol.15
, pp. 340
-
-
Carlier, P.R.1
-
92
-
-
84986835527
-
-
For a related equilibration see
-
For a related equilibration see: H. J. Reich, M. A. Medina, M. D. Bowe, J. Am. Chem. Soc. 1992, 114, 11003.
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 11003
-
-
Reich, H.J.1
Medina, M.A.2
Bowe, M.D.3
-
93
-
-
0141631816
-
-
Subsequent approaches to chiral metalated nitriles have employed noncovalently linked chiral additives: a Y. Suto, N. Kumagai, S. Matsunaga, M. Kanai, M. Shibasaki, Org. Lett. 2003, 5, 3147;
-
Subsequent approaches to chiral metalated nitriles have employed noncovalently linked chiral additives: a) Y. Suto, N. Kumagai, S. Matsunaga, M. Kanai, M. Shibasaki, Org. Lett. 2003, 5, 3147;
-
-
-
-
94
-
-
0031702860
-
-
b) P. R. Carlier, W. W.-F. Lam, N. C. Wan, I. D. Williams, Angew. Chem. Int. Ed. 1998, 37, 2252;
-
(1998)
Angew. Chem. Int. Ed
, vol.37
, pp. 2252
-
-
Carlier, P.R.1
Lam, W.W.-F.2
Wan, N.C.3
Williams, I.D.4
-
96
-
-
0026633940
-
-
d) K. Soai, Y. Hirose, S. Sakata, Tetrahedron: Asymmetry 1992, 3, 677;
-
(1992)
Tetrahedron: Asymmetry
, vol.3
, pp. 677
-
-
Soai, K.1
Hirose, Y.2
Sakata, S.3
-
99
-
-
15444380217
-
-
g) M.-C. Roux, S. Patel, C. G. Mérienne, L. Wartski, G. Morgant, Bull. Chem. Soc. Fr. 1997, 134, 809;
-
(1997)
Bull. Chem. Soc. Fr
, vol.134
, pp. 809
-
-
Roux, M.-C.1
Patel, S.2
Mérienne, C.G.3
Wartski, L.4
Morgant, G.5
-
102
-
-
0030598090
-
-
j) M.-C. Roux, L. Wartski, M. Nierlich, M. Lance, Tetrahedron 1996, 52, 10083;
-
(1996)
Tetrahedron
, vol.52
, pp. 10083
-
-
Roux, M.-C.1
Wartski, L.2
Nierlich, M.3
Lance, M.4
-
103
-
-
0029015249
-
-
k) D. Enders, J. Kirchhoff, D. Mannes, G. Raabe, Synthesis 1995, 659;
-
(1995)
Synthesis
, pp. 659
-
-
Enders, D.1
Kirchhoff, J.2
Mannes, D.3
Raabe, G.4
-
104
-
-
0029002673
-
-
l) C. Cativiela, M. D. Díaz-de-Villegas, J. A. Gálvez, Y. Lapeña, Tetrahedron 1995, 51, 5921;
-
(1995)
Tetrahedron
, vol.51
, pp. 5921
-
-
Cativiela, C.1
Díaz-de-Villegas, M.D.2
Gálvez, J.A.3
Lapeña, Y.4
-
105
-
-
0028200031
-
-
m) C. Cativiela, M. D. Díaz de Villegas, J. A. Gálvez, J. Org. Chem. 1994, 59, 2497;
-
(1994)
J. Org. Chem
, vol.59
, pp. 2497
-
-
Cativiela, C.1
Díaz de Villegas, M.D.2
Gálvez, J.A.3
-
107
-
-
0025349692
-
-
o) D. Enders, P. Gerdes, H. Kipphardt, Angew. Chem. Int. Ed. Engl. 1990, 29, 179;
-
(1990)
Angew. Chem. Int. Ed. Engl
, vol.29
, pp. 179
-
-
Enders, D.1
Gerdes, P.2
Kipphardt, H.3
-
108
-
-
0001408573
-
-
p) T. Hanamoto, T. Katsuki, M. Yamaguchi, Tetrahedron Lett. 1986, 27, 2463;
-
(1986)
Tetrahedron Lett
, vol.27
, pp. 2463
-
-
Hanamoto, T.1
Katsuki, T.2
Yamaguchi, M.3
-
109
-
-
0000030142
-
-
q) J. L. Marco, J. Royer, H.-P. Husson, Tetrahedron Lett. 1985, 26, 3567;
-
(1985)
Tetrahedron Lett
, vol.26
, pp. 3567
-
-
Marco, J.L.1
Royer, J.2
Husson, H.-P.3
-
110
-
-
0000782851
-
-
r) D. Enders, H. Lotter, N. Maigrot, J.-P. Mazaleyrat, Z. Welvart, Nouv. J. Chem. 1984, 8, 747.
-
(1984)
Nouv. J. Chem
, vol.8
, pp. 747
-
-
Enders, D.1
Lotter, H.2
Maigrot, N.3
Mazaleyrat, J.-P.4
Welvart, Z.5
-
113
-
-
0032192409
-
-
a) P. Jankowski, S. Marczak, J. Wicha, Tetrahedron 1998, 54, 12071;
-
(1998)
Tetrahedron
, vol.54
, pp. 12071
-
-
Jankowski, P.1
Marczak, S.2
Wicha, J.3
-
115
-
-
23944525533
-
-
a) V. Singh, S. R. Iyer, S. Pal, Tetrahedron 2005, 61, 9197;
-
(2005)
Tetrahedron
, vol.61
, pp. 9197
-
-
Singh, V.1
Iyer, S.R.2
Pal, S.3
-
118
-
-
33947086979
-
-
a) G. Stork, J. O. Gardner, R. K. Boeckman Jr, K. A. Parker, J. Am. Chem. Soc. 1973, 95, 2014;
-
(1973)
J. Am. Chem. Soc
, vol.95
, pp. 2014
-
-
Stork, G.1
Gardner, J.O.2
Boeckman Jr, R.K.3
Parker, K.A.4
-
120
-
-
0001206209
-
-
Equilibration of decalones is highly substituent-dependent (see [42a]) with some syntheses encountering only modest preferences for one-ring junction stereochemistry (see [42b, 42c]). a) H. W. Thompson, D. J. Long, J. Org. Chem. 1988, 53, 4201;
-
Equilibration of decalones is highly substituent-dependent (see [42a]) with some syntheses encountering only modest preferences for one-ring junction stereochemistry (see [42b, 42c]). a) H. W. Thompson, D. J. Long, J. Org. Chem. 1988, 53, 4201;
-
-
-
-
122
-
-
0001189449
-
-
c) T. Kametani, Y. Kato, T. Honda, K. Fukumoto, J. Am. Chem. Soc. 1976, 98, 8185.
-
(1976)
J. Am. Chem. Soc
, vol.98
, pp. 8185
-
-
Kametani, T.1
Kato, Y.2
Honda, T.3
Fukumoto, K.4
-
124
-
-
57349194797
-
-
The relative stabilities of cis and trans hydrindanes depends on temperature and substitution pattern, with angularly substi tuted cis-hydrindanes generally being more stable than their trans-hydrindane counterparts: E. L. Eliel, S. H. Wilen, L. N. Mander, in Stereochemistry of Organic Compounds, Wiley, NY, 1994, pp. 774-775.
-
The relative stabilities of cis and trans hydrindanes depends on temperature and substitution pattern, with angularly substi tuted cis-hydrindanes generally being more stable than their trans-hydrindane counterparts: E. L. Eliel, S. H. Wilen, L. N. Mander, in Stereochemistry of Organic Compounds, Wiley, NY, 1994, pp. 774-775.
-
-
-
-
125
-
-
34548738189
-
-
a) F. F. Fleming, S. Gudipati, J. Aitken, J. Org. Chem. 2007, 72, 6961;
-
(2007)
J. Org. Chem
, vol.72
, pp. 6961
-
-
Fleming, F.F.1
Gudipati, S.2
Aitken, J.3
-
127
-
-
85010592651
-
-
For a related cyclization to an angular nitrile-containing hydrindane see
-
For a related cyclization to an angular nitrile-containing hydrindane see: M. Sato, T. Suzuki, H. Morisawa, S. Fujita, N. Inukai, C. Kaneko, Chem. Pharm. Bull. 1987, 35, 3647.
-
(1987)
Chem. Pharm. Bull
, vol.35
, pp. 3647
-
-
Sato, M.1
Suzuki, T.2
Morisawa, H.3
Fujita, S.4
Inukai, N.5
Kaneko, C.6
-
128
-
-
33846965282
-
-
a) F. F. Fleming, V. A. Vu, B. C. Shook, M. Rahman, O. W. Steward, J. Org. Chem. 2007, 72, 1431;
-
(2007)
J. Org. Chem
, vol.72
, pp. 1431
-
-
Fleming, F.F.1
Vu, V.A.2
Shook, B.C.3
Rahman, M.4
Steward, O.W.5
-
129
-
-
0037415522
-
-
b) F. F. Fleming, B. C. Shook, T. Jiang, O. W. Steward, Tetrahedron 2003, 59, 737;
-
(2003)
Tetrahedron
, vol.59
, pp. 737
-
-
Fleming, F.F.1
Shook, B.C.2
Jiang, T.3
Steward, O.W.4
-
130
-
-
0033581754
-
-
c) F. F. Fleming, B. C. Shook, T. Jiang, O. W. Steward, Org. Lett. 1999, 1, 1547.
-
(1999)
Org. Lett
, vol.1
, pp. 1547
-
-
Fleming, F.F.1
Shook, B.C.2
Jiang, T.3
Steward, O.W.4
-
131
-
-
0037204694
-
-
Use of the lithium alkoxide is critical because the magnesium alkoxide readily eliminates: a F. F. Fleming, B. C. Shook, J. Org. Chem. 2002, 67, 3668;
-
Use of the lithium alkoxide is critical because the magnesium alkoxide readily eliminates: a) F. F. Fleming, B. C. Shook, J. Org. Chem. 2002, 67, 3668;
-
-
-
-
134
-
-
0034736354
-
-
b) F. A. Davis, P. K. Mohanty, D. M. Burns, Y. W. Andemichael, Org. Lett. 2000, 2, 3901;
-
(2000)
Org. Lett
, vol.2
, pp. 3901
-
-
Davis, F.A.1
Mohanty, P.K.2
Burns, D.M.3
Andemichael, Y.W.4
-
135
-
-
0346520789
-
-
c) T. Schrader, C. Kirsten, M. Herm, Phosphorous, Sulfur Silicon 1999, 144-146, 161;
-
(1999)
Phosphorous, Sulfur Silicon
, vol.144-146
, pp. 161
-
-
Schrader, T.1
Kirsten, C.2
Herm, M.3
-
138
-
-
0033235147
-
-
a) F. Kakiuchi, M. Sonoda, T. Tsujimoto, N. Chatani, S. Murai, Chem. Lett. 1999, 1083;
-
(1999)
Chem. Lett
, pp. 1083
-
-
Kakiuchi, F.1
Sonoda, M.2
Tsujimoto, T.3
Chatani, N.4
Murai, S.5
-
140
-
-
0035930002
-
-
For a related interaction between fluorine and the nitrile π-electrons see
-
For a related interaction between fluorine and the nitrile π-electrons see: K. Nishide, Y. Hagimoto, H. Hasegawa, M. Shiro, M. Node, Chem. Commun. 2001, 2394.
-
(2001)
Chem. Commun
, pp. 2394
-
-
Nishide, K.1
Hagimoto, Y.2
Hasegawa, H.3
Shiro, M.4
Node, M.5
-
141
-
-
0033550167
-
-
Chelation of nitriles by lithium cations is directly analogous to the chelation of organolithiums with proximal alkenes and aromatic π systems: a C. R. Harris, S. J. Danishefsky, J. Org. Chem. 1999, 64, 8434;
-
Chelation of nitriles by lithium cations is directly analogous to the chelation of organolithiums with proximal alkenes and aromatic π systems: a) C. R. Harris, S. J. Danishefsky, J. Org. Chem. 1999, 64, 8434;
-
-
-
-
143
-
-
0000576830
-
-
c) W. F. Bailey, A. D. Khanolkar, K. Gavaskar, T. V. Ovaska, K. Rossi, Y. Thiel, K. B. Wiberg, J. Am. Chem. Soc. 1991, 113, 5720.
-
(1991)
J. Am. Chem. Soc
, vol.113
, pp. 5720
-
-
Bailey, W.F.1
Khanolkar, A.D.2
Gavaskar, K.3
Ovaska, T.V.4
Rossi, K.5
Thiel, Y.6
Wiberg, K.B.7
-
144
-
-
45549122288
-
-
F. F. Fleming, Y. Wei, W. Liu, Z. Zhang, Tetrahedron 2008, 64, 7477.
-
(2008)
Tetrahedron
, vol.64
, pp. 7477
-
-
Fleming, F.F.1
Wei, Y.2
Liu, W.3
Zhang, Z.4
-
147
-
-
0342735472
-
-
Analogous CuIII species were verified as key intermediates during coupling of lithium dimethyl cuprate with halobenzenes (see [55a, although the lifetime of this intermediate may be short since a CuIII intermediate was not detected by 13C NMR during the reaction of Me2CuLi with 1-bromocyclooctene (see [55b, a) W. J. Spanenburg, B. E. Snell, M.-C. Su, Microchem. J. 1993, 47, 79;
-
2CuLi with 1-bromocyclooctene (see [55b]). a) W. J. Spanenburg, B. E. Snell, M.-C. Su, Microchem. J. 1993, 47, 79;
-
-
-
-
149
-
-
57349181889
-
-
[3]).
-
[3]).
-
-
-
-
150
-
-
0000717185
-
-
a) K. A. Swiss, D. C. Liotta, C. A. Maryanoff, J. Am. Chem. Soc. 1990, 112, 9393;
-
(1990)
J. Am. Chem. Soc
, vol.112
, pp. 9393
-
-
Swiss, K.A.1
Liotta, D.C.2
Maryanoff, C.A.3
|