-
2
-
-
61949285610
-
-
For physicochemical properties and reactivity profiles of methyl and ethyl propiolate:, Ed, L. A. Paquette, Wiley, New York
-
For physicochemical properties and reactivity profiles of methyl and ethyl propiolate: G. C. Hirst in Encyclopedia of Reagents for Organic Synthesis, Vol. 5 (Ed.: L. A. Paquette), Wiley, New York, 1995, pp. 3576-3578.
-
(1995)
Encyclopedia of Reagents for Organic Synthesis
, vol.5
, pp. 3576-3578
-
-
Hirst, G.C.1
-
6
-
-
41849102732
-
-
For β-oniovinylations
-
a) For β-oniovinylations: R. Weiss, M. Bess, S. M. Huber, F. W. Heinemann, J. Am. Chem. Soc. 2008, 130, 4610-4617;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 4610-4617
-
-
Weiss, R.1
Bess, M.2
Huber, S.M.3
Heinemann, F.W.4
-
7
-
-
0037366617
-
-
for a recent review on Baylis-Hillman reactions, including terminal alkynoates: D. Basavaiah, A. J. Rao, T. Satyanarayana, Chem. Rev. 2003, 103, 811-891.
-
b) for a recent review on Baylis-Hillman reactions, including terminal alkynoates: D. Basavaiah, A. J. Rao, T. Satyanarayana, Chem. Rev. 2003, 103, 811-891.
-
-
-
-
8
-
-
0002085548
-
-
M. M. Midland, A. Tramontano, J. R. Cable, J. Org. Chem. 1980, 45, 28-29.
-
(1980)
J. Org. Chem
, vol.45
, pp. 28-29
-
-
Midland, M.M.1
Tramontano, A.2
Cable, J.R.3
-
9
-
-
85066064403
-
-
K. Yamada, N. Miyaura, M. Itoh, A. Suzuki, Synthesis 1977, 679-682.
-
(1977)
Synthesis
, pp. 679-682
-
-
Yamada, K.1
Miyaura, N.2
Itoh, M.3
Suzuki, A.4
-
10
-
-
61949189369
-
-
Special issue: Frontiers in organic synthesis (Ed.: P. A. Wender), Chem. Rev. 1996, 96, 1-600.
-
a) Special issue: "Frontiers in organic synthesis" (Ed.: P. A. Wender), Chem. Rev. 1996, 96, 1-600.
-
-
-
-
11
-
-
84869243496
-
-
Lithiated methyl propiolate decomposes at temperatures above -100°C, whereas the ethyl ester is stable up -78°C.
-
Lithiated methyl propiolate decomposes at temperatures above -100°C, whereas the ethyl ester is stable up -78°C.
-
-
-
-
12
-
-
38349004628
-
-
For selected recent examples: a
-
For selected recent examples: a) W. He, J. Huang, X. Sun, A. J. Frontier, J. Am. Chem. Soc. 2008, 130, 300-308;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 300-308
-
-
He, W.1
Huang, J.2
Sun, X.3
Frontier, A.J.4
-
13
-
-
38749107646
-
-
b) T. Taniguchi, G. Tanabe, O. Muraoka, H. Ishibashi, Org. Lett. 2008, 10, 197-199;
-
(2008)
Org. Lett
, vol.10
, pp. 197-199
-
-
Taniguchi, T.1
Tanabe, G.2
Muraoka, O.3
Ishibashi, H.4
-
14
-
-
33846462087
-
-
c) W. He, J. Huang, X. Sun, A. J. Frontier, J. Am. Chem. Soc. 2007, 129, 498-499;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 498-499
-
-
He, W.1
Huang, J.2
Sun, X.3
Frontier, A.J.4
-
15
-
-
33750483918
-
-
d) C.-C. Li, C.-H. Wang, B. Liang, X.-H. Zhang, L.-J. Deng, S. Liang, J.-H. Chen, Y.-D. Wu, Z. Yang, J. Org. Chem. 2006, 71, 6892-6897;
-
(2006)
J. Org. Chem
, vol.71
, pp. 6892-6897
-
-
Li, C.-C.1
Wang, C.-H.2
Liang, B.3
Zhang, X.-H.4
Deng, L.-J.5
Liang, S.6
Chen, J.-H.7
Wu, Y.-D.8
Yang, Z.9
-
19
-
-
0037077074
-
-
h) Y.-G. Suh, J.-K. Jung, S.-Y. Seo, K.-H. Min, D.-Y. Shin, Y.-S. Lee, S.-H. Kim, H.-J. Park, J. Org. Chem. 2002, 67, 4127-4137;
-
(2002)
J. Org. Chem
, vol.67
, pp. 4127-4137
-
-
Suh, Y.-G.1
Jung, J.-K.2
Seo, S.-Y.3
Min, K.-H.4
Shin, D.-Y.5
Lee, Y.-S.6
Kim, S.-H.7
Park, H.-J.8
-
20
-
-
0033824824
-
-
i) M. T. Crimmins, J. M. Pace, P. G. Nantermet, A. S. Kim-Meade, J. B. Thomas, S. H. Watterson, A. S. Wagman, J. Am. Chem. Soc. 2000, 122, 8453-8463.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 8453-8463
-
-
Crimmins, M.T.1
Pace, J.M.2
Nantermet, P.G.3
Kim-Meade, A.S.4
Thomas, J.B.5
Watterson, S.H.6
Wagman, A.S.7
-
21
-
-
0034112410
-
-
and references cited therein
-
P. Merino, S. Franco, F. L. Mercham, T. Tejero, Synlett 2000, 442-454 and references cited therein.
-
(2000)
Synlett
, pp. 442-454
-
-
Merino, P.1
Franco, S.2
Mercham, F.L.3
Tejero, T.4
-
22
-
-
0344514158
-
-
a) S. K. Patel, K. Murat, S. Py, Y. Vallée, Org. Lett. 2003, 5, 4081-4084;
-
(2003)
Org. Lett
, vol.5
, pp. 4081-4084
-
-
Patel, S.K.1
Murat, K.2
Py, S.3
Vallée, Y.4
-
23
-
-
0030792964
-
-
b) J.-N. Denis, S. Tchertchian, A. Tomassini, Y. Vallée, Tetrahedron Lett. 1997, 38, 5503-5506.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 5503-5506
-
-
Denis, J.-N.1
Tchertchian, S.2
Tomassini, A.3
Vallée, Y.4
-
24
-
-
0036569586
-
-
S. Hanessian, M. Bayrakdarian, X. Luo, J. Am. Chem. Soc. 2002, 124, 4716-4721.
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 4716-4721
-
-
Hanessian, S.1
Bayrakdarian, M.2
Luo, X.3
-
25
-
-
34447338012
-
-
D. Tejedor, S. López-Tosco, J. González-Platas, F. García-Tellado, J. Org. Chem. 2007, 72, 5454-5456.
-
(2007)
J. Org. Chem
, vol.72
, pp. 5454-5456
-
-
Tejedor, D.1
López-Tosco, S.2
González-Platas, J.3
García-Tellado, F.4
-
27
-
-
33746868887
-
-
For an addition with a different outcome
-
For an addition with a different outcome: T. Person, J. Nielsen, Org. Lett. 2006, 8, 3219-3222.
-
(2006)
Org. Lett
, vol.8
, pp. 3219-3222
-
-
Person, T.1
Nielsen, J.2
-
28
-
-
0035825796
-
-
D. L. Comins, S. Huang, C. L. McArdle, C. L. Ingalls, Org. Lett. 2001, 3, 469-471.
-
(2001)
Org. Lett
, vol.3
, pp. 469-471
-
-
Comins, D.L.1
Huang, S.2
McArdle, C.L.3
Ingalls, C.L.4
-
29
-
-
0034617818
-
-
3-homologation of α-hydroxy aldehydes using magnesium acetylides: D. L. J. Clive, Y. Tao, Y. Bo, Y.-Z. Hu, N. Selvakumar, S. Sun, S. Daigneault, Y.-J. Wu, Chem. Commun. 2000, 1341-1350.
-
3-homologation of α-hydroxy aldehydes using magnesium acetylides: D. L. J. Clive, Y. Tao, Y. Bo, Y.-Z. Hu, N. Selvakumar, S. Sun, S. Daigneault, Y.-J. Wu, Chem. Commun. 2000, 1341-1350.
-
-
-
-
30
-
-
33746766250
-
-
For the stereoselective addition of zinc acetylides to Garner's aldehyde: S. Hanessian, G. Yang, J.-M. Rondeau, U. Neumann, C. Betschart, M. Tintelnot-Blomley, J. Med. Chem. 2006, 49, 4544-4567.
-
For the stereoselective addition of zinc acetylides to Garner's aldehyde: S. Hanessian, G. Yang, J.-M. Rondeau, U. Neumann, C. Betschart, M. Tintelnot-Blomley, J. Med. Chem. 2006, 49, 4544-4567.
-
-
-
-
31
-
-
0035807527
-
-
2) coupling reaction of alkyl propiolates and aryl halides: a) L. Anastasia, E. Negishi, Org. Lett. 2001, 3, 3111-3113;
-
2) coupling reaction of alkyl propiolates and aryl halides: a) L. Anastasia, E. Negishi, Org. Lett. 2001, 3, 3111-3113;
-
-
-
-
32
-
-
4444243019
-
-
b) K. Hiroya, S. Matsumoto, T. Sakamoto, Org. Lett. 2004, 6, 2953-2956.
-
(2004)
Org. Lett
, vol.6
, pp. 2953-2956
-
-
Hiroya, K.1
Matsumoto, S.2
Sakamoto, T.3
-
33
-
-
0141630352
-
-
For an example of a palladium(0)-catalyzed cross-coupling reaction of methyl propiolate and α-iodoenamides
-
For an example of a palladium(0)-catalyzed cross-coupling reaction of methyl propiolate and α-iodoenamides: J. A. Mulder, K. C. Kurtz, R. P. Hsung, H. Coverdale, M. O. Frederick, L. Shen, C. A. Zificsak, Org. Lett. 2003, 5, 1547-1550.
-
(2003)
Org. Lett
, vol.5
, pp. 1547-1550
-
-
Mulder, J.A.1
Kurtz, K.C.2
Hsung, R.P.3
Coverdale, H.4
Frederick, M.O.5
Shen, L.6
Zificsak, C.A.7
-
34
-
-
0037424281
-
-
For a diastereoselective addition of methyl propiolate to chiral nitrones in the presence of catalytic amounts of Et2Zn: a S. K. Patel, S. Py, S. U. Pandya, P. Y. Chavant, Y. Vallée, Tetrahedron: Asymmetry 2003, 14, 525-528;
-
2Zn: a) S. K. Patel, S. Py, S. U. Pandya, P. Y. Chavant, Y. Vallée, Tetrahedron: Asymmetry 2003, 14, 525-528;
-
-
-
-
35
-
-
0013079244
-
-
b) S. Pinet, S. U Pandya, P. Y. Chavant, A. Ayling, Y. Valle, Org. Lett. 2002, 4, 1463-1466.
-
(2002)
Org. Lett
, vol.4
, pp. 1463-1466
-
-
Pinet, S.1
Pandya, S.U.2
Chavant, P.Y.3
Ayling, A.4
Valle, Y.5
-
36
-
-
23644433348
-
-
For cerium acetylide additions to functionalized aldehydes: a
-
For cerium acetylide additions to functionalized aldehydes: a) S. Hanessian, H. Yun, Y. Hou, M. Tintelnot-Blomley, J. Org. Chem. 2005, 70, 6746-6756;
-
(2005)
J. Org. Chem
, vol.70
, pp. 6746-6756
-
-
Hanessian, S.1
Yun, H.2
Hou, Y.3
Tintelnot-Blomley, M.4
-
37
-
-
0033835583
-
-
b) E. Vedjes, D. W. Piotrowski, F. C. Tucci, J. Org. Chem. 2000, 65, 5498-5505.
-
(2000)
J. Org. Chem
, vol.65
, pp. 5498-5505
-
-
Vedjes, E.1
Piotrowski, D.W.2
Tucci, F.C.3
-
38
-
-
36049050141
-
-
For recent selected examples of boron-promoted epoxide opening with alkyl propiolates: a
-
For recent selected examples of boron-promoted epoxide opening with alkyl propiolates: a) C. D. Donner, Tetrahedron Lett. 2007, 48, 8888-8890;
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 8888-8890
-
-
Donner, C.D.1
-
39
-
-
33750881162
-
-
b) G. S. Kauffman, P. S. Watson, W. A. Nugent, J. Org. Chem. 2006, 71, 8975-8977;
-
(2006)
J. Org. Chem
, vol.71
, pp. 8975-8977
-
-
Kauffman, G.S.1
Watson, P.S.2
Nugent, W.A.3
-
40
-
-
25444465477
-
-
c) C. V. Ramana, B. Srinivas, V. G. Puranik, M. K. Gurjar, J. Org. Chem. 2005, 70, 8216-8219;
-
(2005)
J. Org. Chem
, vol.70
, pp. 8216-8219
-
-
Ramana, C.V.1
Srinivas, B.2
Puranik, V.G.3
Gurjar, M.K.4
-
41
-
-
7044260712
-
-
d) M. Ball, A. Baron, B. Bradshaw, H. Omori, S. MacCormick, E. J. Thomas, Tetrahedron Lett. 2004, 45, 8737-8740;
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 8737-8740
-
-
Ball, M.1
Baron, A.2
Bradshaw, B.3
Omori, H.4
MacCormick, S.5
Thomas, E.J.6
-
43
-
-
0034641440
-
-
f) E. K. Dorling, E. Öhler, J. Mulzer, Tetrahedron Lett. 2000, 41, 6323-6326;
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 6323-6326
-
-
Dorling, E.K.1
Öhler, E.2
Mulzer, J.3
-
44
-
-
29344448010
-
-
for a study on the regioselectivity in the opening of bhydroxy epoxides using different metal acetylides: B. M. Trost, J. P. N. Papillon, T. Nussbaumer, J. Am. Chem. Soc. 2005, 127, 17921-17937
-
g) for a study on the regioselectivity in the opening of bhydroxy epoxides using different metal acetylides: B. M. Trost, J. P. N. Papillon, T. Nussbaumer, J. Am. Chem. Soc. 2005, 127, 17921-17937.
-
-
-
-
45
-
-
61949405978
-
-
A survey of good examples can be found in references [10-13, 19, 22, 23
-
A survey of good examples can be found in references [10-13, 19, 22, 23].
-
-
-
-
48
-
-
34247555417
-
-
U. Halbes-Letinois, J.-M. Weibel, P. Pale, Chem. Soc. Rev. 2007, 36, 759-769.
-
(2007)
Chem. Soc. Rev
, vol.36
, pp. 759-769
-
-
Halbes-Letinois, U.1
Weibel, J.-M.2
Pale, P.3
-
50
-
-
2942596792
-
-
Angew. Chem. Int. Ed. 2004, 43, 2525-2527.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 2525-2527
-
-
-
51
-
-
0037433972
-
-
Silver acetylides react with acid chlorides to afford the corresponding propargylic ketones 3. T. Naka, K. Koide, Tetrahedron Lett. 2003, 44, 443-445.
-
Silver acetylides react with acid chlorides to afford the corresponding propargylic ketones 3. T. Naka, K. Koide, Tetrahedron Lett. 2003, 44, 443-445.
-
-
-
-
52
-
-
33644959352
-
-
B. J. Albert, A. Sivaramakrishnan, T. Naka, K. Koide, J. Am. Chem. Soc. 2006, 128, 2792-2793.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 2792-2793
-
-
Albert, B.J.1
Sivaramakrishnan, A.2
Naka, T.3
Koide, K.4
-
53
-
-
0242635970
-
-
For selected reviews: a
-
For selected reviews: a) L. Pu, Tetrahedron 2003, 59, 9873-9886;
-
(2003)
Tetrahedron
, vol.59
, pp. 9873-9886
-
-
Pu, L.1
-
54
-
-
84890980810
-
-
Eds, F. Diederich, P. J. Stang, R. R. Tykwinski, Wiley-VCH, Weinheim
-
b) P. Aschwanden, E. M. Carreira in Acetylene Chemistry. Chemistry, Biology, and Material Science (Eds.: F. Diederich, P. J. Stang, R. R. Tykwinski), Wiley-VCH, Weinheim, 2005, pp. 101-138.
-
(2005)
Acetylene Chemistry. Chemistry, Biology, and Material Science
, pp. 101-138
-
-
Aschwanden, P.1
Carreira, E.M.2
-
56
-
-
0041407526
-
-
b) D. E. Frantz, R. Fassler, E. M. Carreira, J. Am. Chem. Soc. 2000, 122, 1806-1807;
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 1806-1807
-
-
Frantz, D.E.1
Fassler, R.2
Carreira, E.M.3
-
57
-
-
0038252959
-
-
c) D. E. Frantz, R. Fassler, C. S. Tomoka, E. M. Carreira, Acc. Chem. Res. 2000, 33, 373-381.
-
(2000)
Acc. Chem. Res
, vol.33
, pp. 373-381
-
-
Frantz, D.E.1
Fassler, R.2
Tomoka, C.S.3
Carreira, E.M.4
-
58
-
-
34250738498
-
-
a) G. Gao, Q. Wang, X.-Q. Yu, R.-G. Xie, L. Pu, Angew. Chem. 2005, 118, 128-131;
-
(2005)
Angew. Chem
, vol.118
, pp. 128-131
-
-
Gao, G.1
Wang, Q.2
Yu, X.-Q.3
Xie, R.-G.4
Pu, L.5
-
60
-
-
33744770021
-
-
for a synthetic application
-
b) for a synthetic application: A. R. Rajaram, L. Pu, Org. Lett. 2006, 8, 2019-2021.
-
(2006)
Org. Lett
, vol.8
, pp. 2019-2021
-
-
Rajaram, A.R.1
Pu, L.2
-
61
-
-
1842681980
-
-
and references cited therein
-
a) G. Gao, R.-G. Xie, L. Pu, Proc. Natl. Acad. Sci. USA 2004, 101, 5417-5420, and references cited therein.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 5417-5420
-
-
Gao, G.1
Xie, R.-G.2
Pu, L.3
-
62
-
-
33747790856
-
-
Y.-C. Qin, L. Liu, M. Sabat, L. Pu, Tetrahedron 2006, 62, 9335-9348.
-
(2006)
Tetrahedron
, vol.62
, pp. 9335-9348
-
-
Qin, Y.-C.1
Liu, L.2
Sabat, M.3
Pu, L.4
-
63
-
-
34447335324
-
-
F. Yang, P. Xi, L. Yang, J. Lan, R. Xie, J. You, J. Org. Chem. 2007, 72, 5457-5460.
-
(2007)
J. Org. Chem
, vol.72
, pp. 5457-5460
-
-
Yang, F.1
Xi, P.2
Yang, L.3
Lan, J.4
Xie, R.5
You, J.6
-
64
-
-
34250792753
-
-
L. Lin, X. Jiang, W. Liu, L. Qiu, Z. Xu, J. Xu, A. S. C. Chan, R. Wang, Org. Lett. 2007, 9, 2329-2332.
-
(2007)
Org. Lett
, vol.9
, pp. 2329-2332
-
-
Lin, L.1
Jiang, X.2
Liu, W.3
Qiu, L.4
Xu, Z.5
Xu, J.6
Chan, A.S.C.7
Wang, R.8
-
65
-
-
30744477996
-
-
B. M. Trost, A. H. Weiss, A. Jacobi von Wangelin, J. Am. Chem. Soc. 2006, 128, 8-9.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 8-9
-
-
Trost, B.M.1
Weiss, A.H.2
Jacobi von Wangelin, A.3
-
67
-
-
34547659128
-
-
Z. Sun, S. Yu, Z. Ding, D. Ma, J. Am. Chem. Soc. 2007, 129, 9300-9301.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 9300-9301
-
-
Sun, Z.1
Yu, S.2
Ding, Z.3
Ma, D.4
-
68
-
-
41149135082
-
-
The procedure has been recently generalized to incorporate non-conjugated terminal alkynes and other pyridine-based heterocycles. D. A. Black, R. E. Beveridge, B. A. Arndtsen, J. Org. Chem. 2008, 73, 1906-1910
-
The procedure has been recently generalized to incorporate non-conjugated terminal alkynes and other pyridine-based heterocycles. D. A. Black, R. E. Beveridge, B. A. Arndtsen, J. Org. Chem. 2008, 73, 1906-1910.
-
-
-
-
69
-
-
33646245219
-
-
M.-C. Ye, J. Zhou, Y. Tang, J. Org. Chem. 2006, 71, 3576-3582.
-
(2006)
J. Org. Chem
, vol.71
, pp. 3576-3582
-
-
Ye, M.-C.1
Zhou, J.2
Tang, Y.3
-
71
-
-
34447295387
-
-
Angew. Chem. Int. Ed. 2007, 46, 4964-4967.
-
(2007)
Angew. Chem. Int. Ed
, vol.46
, pp. 4964-4967
-
-
-
75
-
-
0037414541
-
-
T. Ishikawa, T. Mizuta, K. Hagiwara, T. Aikawa, T. Kudo, S. Saito, J. Org. Chem. 2003, 68, 3702-3705.
-
(2003)
J. Org. Chem
, vol.68
, pp. 3702-3705
-
-
Ishikawa, T.1
Mizuta, T.2
Hagiwara, K.3
Aikawa, T.4
Kudo, T.5
Saito, S.6
-
76
-
-
20444500603
-
-
D. Tejedor, D. González-Cruz, A. Sántos-Expósito, J. J. Marrero-Tellado, P. Armas, F. García-Tellado, Chem. Eur. J. 2005, 11, 3502-3510.
-
(2005)
Chem. Eur. J
, vol.11
, pp. 3502-3510
-
-
Tejedor, D.1
González-Cruz, D.2
Sántos-Expósito, A.3
Marrero-Tellado, J.J.4
Armas, P.5
García-Tellado, F.6
-
77
-
-
33745192797
-
-
Electrophiles must be less acidic than the alkyl propiolate itself to allow the acetylide formation and consequently the corresponding domino processes. D. Tejedor, A. Santos-Expósito, F. García-Tellado, Chem. Commun. 2006, 2667-2669
-
Electrophiles must be less acidic than the alkyl propiolate itself to allow the acetylide formation and consequently the corresponding domino processes. D. Tejedor, A. Santos-Expósito, F. García-Tellado, Chem. Commun. 2006, 2667-2669.
-
-
-
-
78
-
-
0042307518
-
-
For domino reactions with alkyl propiolates and aldehydes or activated ketones: a
-
For domino reactions with alkyl propiolates and aldehydes or activated ketones: a) D. Tejedor, F. García-Tellado, J. J. Marrero-Tellado, P. de Armas, Chem. Eur. J. 2003, 9, 3122-3131;
-
(2003)
Chem. Eur. J
, vol.9
, pp. 3122-3131
-
-
Tejedor, D.1
García-Tellado, F.2
Marrero-Tellado, J.J.3
de Armas, P.4
-
79
-
-
18044404544
-
-
b) P. de Armas, F. García-Tellado, J. J. Marrero-Tellado, D. Tejedor, M. A. Maestro, J. González-Platas, Org. Lett. 2001, 3, 1905-1908.
-
(2001)
Org. Lett
, vol.3
, pp. 1905-1908
-
-
de Armas, P.1
García-Tellado, F.2
Marrero-Tellado, J.J.3
Tejedor, D.4
Maestro, M.A.5
González-Platas, J.6
-
80
-
-
33846579646
-
-
For domino reactions with alkyl propiolates and 1,2-ketoesters or 1,2-ketoamides
-
For domino reactions with alkyl propiolates and 1,2-ketoesters or 1,2-ketoamides: D. Tejedor, A. Santos-Expósito, F. García-Tellado, Chem. Eur. J. 2007, 13, 1201-1209.
-
(2007)
Chem. Eur. J
, vol.13
, pp. 1201-1209
-
-
Tejedor, D.1
Santos-Expósito, A.2
García-Tellado, F.3
-
81
-
-
13244267096
-
-
a) D. Tejedor, A. Santos-Expósito, D. González-Cruz, F. García-Tellado, J. J. Marrero-Tellado, J. Org. Chem. 2005, 70, 1042-1045;
-
(2005)
J. Org. Chem
, vol.70
, pp. 1042-1045
-
-
Tejedor, D.1
Santos-Expósito, A.2
González-Cruz, D.3
García-Tellado, F.4
Marrero-Tellado, J.J.5
-
82
-
-
3142724941
-
-
b) D. Tejedor, D. González-Cruz, F. García-Tellado, J. J. Marrero-Tellado, M. L. Rodríguez, J. Am. Chem. Soc. 2004, 126, 8390-8391;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 8390-8391
-
-
Tejedor, D.1
González-Cruz, D.2
García-Tellado, F.3
Marrero-Tellado, J.J.4
Rodríguez, M.L.5
-
83
-
-
0345381993
-
-
c) D. T. Aragón, G. V. López, F. García-Tellado, J. J. Marrero-Tellado, P. De Armas, D. Terrero, J. Org. Chem. 2003, 68, 3363-3365.
-
(2003)
J. Org. Chem
, vol.68
, pp. 3363-3365
-
-
Aragón, D.T.1
López, G.V.2
García-Tellado, F.3
Marrero-Tellado, J.J.4
De Armas, P.5
Terrero, D.6
-
84
-
-
34250327977
-
-
3N as catalysts. D. González-Cruz, D. Tejedor, P. de Armas, F. García-Tellado, Chem. Eur. J. 2007, 13, 4823-4832.
-
3N as catalysts. D. González-Cruz, D. Tejedor, P. de Armas, F. García-Tellado, Chem. Eur. J. 2007, 13, 4823-4832.
-
-
-
-
85
-
-
33847274696
-
-
For full details and more examples of this type of MCRs, see
-
For full details and more examples of this type of MCRs, see: D. Tejedor, F. García-Tellado, Chem. Soc. Rev. 2007, 36, 484-491.
-
(2007)
Chem. Soc. Rev
, vol.36
, pp. 484-491
-
-
Tejedor, D.1
García-Tellado, F.2
-
86
-
-
33646455592
-
-
a) Y.-G. Wang, S.-L. Cui, X.-F. Lin, Org. Lett. 2006, 8, 1241-1244;
-
(2006)
Org. Lett
, vol.8
, pp. 1241-1244
-
-
Wang, Y.-G.1
Cui, S.-L.2
Lin, X.-F.3
|