-
1
-
-
73349100031
-
-
Afagh, N. A.; Yudin, A. K. Angew. Chem., Int. Ed. 2010, 49, 262-310
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 262-310
-
-
Afagh, N.A.1
Yudin, A.K.2
-
4
-
-
0034607293
-
-
Myers, A. G.; Kung, D. W.; Zhong, B. J. Am. Chem. Soc. 2000, 122, 3236-3237
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 3236-3237
-
-
Myers, A.G.1
Kung, D.W.2
Zhong, B.3
-
5
-
-
0037454306
-
-
Ooi, T.; Saito, A.; Maruoka, K. J. Am. Chem. Soc. 2003, 125, 3220-3221
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 3220-3221
-
-
Ooi, T.1
Saito, A.2
Maruoka, K.3
-
6
-
-
64849117664
-
-
Sivaraj, B.; Hili, R.; Yudin, A. K. Aldrichimia Acta 2008, 41, 109-119
-
(2008)
Aldrichimia Acta
, vol.41
, pp. 109-119
-
-
Sivaraj, B.1
Hili, R.2
Yudin, A.K.3
-
9
-
-
33748241815
-
-
Enders, D.; Funk, R.; Klatt, M.; Raabe, G.; Hovestreydt, E. R. Angew. Chem., Int. Ed. Engl. 1993, 32, 418-421
-
(1993)
Angew. Chem., Int. Ed. Engl.
, vol.32
, pp. 418-421
-
-
Enders, D.1
Funk, R.2
Klatt, M.3
Raabe, G.4
Hovestreydt, E.R.5
-
11
-
-
0028149915
-
-
Muralidharan, K. R.; Mokhallalati, M. K.; Pridgen, L. N. Tetrahedron Lett. 1994, 35, 7489-7492
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 7489-7492
-
-
Muralidharan, K.R.1
Mokhallalati, M.K.2
Pridgen, L.N.3
-
12
-
-
0029117516
-
-
Alexakis, A.; Lensen, N.; Tranchier, J.-P.; Mangeney, P.; Feneau- Dupont, J.; Declercq, J. P. Synthesis 1995, 1038-1049
-
(1995)
Synthesis
, pp. 1038-1049
-
-
Alexakis, A.1
Lensen, N.2
Tranchier, J.-P.3
Mangeney, P.4
Feneau- Dupont, J.5
Declercq, J.P.6
-
13
-
-
0033617465
-
-
Myers, A. G.; Schnider, P.; Kwon, S.; Kung, D. W. J. Org. Chem. 1999, 64, 3322-3327
-
(1999)
J. Org. Chem.
, vol.64
, pp. 3322-3327
-
-
Myers, A.G.1
Schnider, P.2
Kwon, S.3
Kung, D.W.4
-
14
-
-
0029989131
-
-
Myers, A. G.; Yang, B. H.; Kopecky, D. J. Tetrahedron Lett. 1996, 37, 3623-3626
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 3623-3626
-
-
Myers, A.G.1
Yang, B.H.2
Kopecky, D.J.3
-
15
-
-
0033568504
-
-
Myers, A. G.; Kung, D. W.; Zong, B.; Movassaghi, M.; Kwon, S. J. Am. Chem. Soc. 1999, 121, 8401-8402
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 8401-8402
-
-
Myers, A.G.1
Kung, D.W.2
Zong, B.3
Movassaghi, M.4
Kwon, S.5
-
16
-
-
0034687186
-
-
Myers, A. G.; Zhong, B.; Kung, D. W.; Movassaghi, M.; Lanman, B. A.; Kwon, S. Org. Lett. 2000, 2, 3337-3340
-
(2000)
Org. Lett.
, vol.2
, pp. 3337-3340
-
-
Myers, A.G.1
Zhong, B.2
Kung, D.W.3
Movassaghi, M.4
Lanman, B.A.5
Kwon, S.6
-
17
-
-
0034716554
-
-
Myers, A.; Zhong, B.; Movassaghi, M.; Kung, D. Tetrahedron Lett. 2000, 41, 1359-1362
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 1359-1362
-
-
Myers, A.1
Zhong, B.2
Movassaghi, M.3
Kung, D.4
-
19
-
-
0000341555
-
-
Rittle, K. E.; Homick, C. F.; Ponticello, G. S.; Evans, B. E. J. Org. Chem. 1982, 47, 3016-3018
-
(1982)
J. Org. Chem.
, vol.47
, pp. 3016-3018
-
-
Rittle, K.E.1
Homick, C.F.2
Ponticello, G.S.3
Evans, B.E.4
-
20
-
-
0038650519
-
-
Gryko, D.; Chako, J.; Jurczak, J. Chirality 2003, 15, 514-541
-
(2003)
Chirality
, vol.15
, pp. 514-541
-
-
Gryko, D.1
Chako, J.2
Jurczak, J.3
-
22
-
-
55049133221
-
-
Hili, R.; Baktharaman, S.; Yudin, A. K. Eur. J. Org. Chem. 2008, 31, 5201-5213
-
(2008)
Eur. J. Org. Chem.
, vol.31
, pp. 5201-5213
-
-
Hili, R.1
Baktharaman, S.2
Yudin, A.K.3
-
23
-
-
47049100483
-
-
Hili, R.; Yudin, A. K. Angew. Chem., Int. Ed. 2008, 47, 4188-4191
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 4188-4191
-
-
Hili, R.1
Yudin, A.K.2
-
24
-
-
77950402397
-
-
Hili, R.; Rai, V.; Yudin, A. K. J. Am. Chem. Soc. 2010, 132, 2889-2891
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 2889-2891
-
-
Hili, R.1
Rai, V.2
Yudin, A.K.3
-
27
-
-
77649099610
-
-
He, Z.; Yudin, A. K. Angew. Chem., Int. Ed. 2010, 49, 1607-1610
-
(2010)
Angew. Chem., Int. Ed.
, vol.49
, pp. 1607-1610
-
-
He, Z.1
Yudin, A.K.2
-
28
-
-
74949090496
-
-
Baktharaman, S.; Afagh, N.; Vandersteen, A.; Yudin, A. K. Org. Lett. 2010, 12, 240-243
-
(2010)
Org. Lett.
, vol.12
, pp. 240-243
-
-
Baktharaman, S.1
Afagh, N.2
Vandersteen, A.3
Yudin, A.K.4
-
29
-
-
82455175693
-
-
Cheung, L. L. W.; He, Z.; Decker, S. M.; Yudin, A. K. Angew. Chem., Int. Ed. 2011, 50, 11798-11802
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 11798-11802
-
-
Cheung, L.L.W.1
He, Z.2
Decker, S.M.3
Yudin, A.K.4
-
32
-
-
78049381974
-
-
Rotstein, B. H.; Rai, V.; Hili, R.; Yudin, A. K. Nat. Protoc. 2010, 5, 1813-1822
-
(2010)
Nat. Protoc.
, vol.5
, pp. 1813-1822
-
-
Rotstein, B.H.1
Rai, V.2
Hili, R.3
Yudin, A.K.4
-
33
-
-
34250318651
-
-
Hodgson, D. M.; Humphreys, P. G.; Xu, Z.; Ward, J. G. Angew. Chem., Int. Ed. 2007, 46, 2245-2248
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 2245-2248
-
-
Hodgson, D.M.1
Humphreys, P.G.2
Xu, Z.3
Ward, J.G.4
-
34
-
-
0002054640
-
Aziridines and azirines: Monocyclic
-
In; Katritzky, A. R. Rees, C. W. Scriven, E. F. V. Elsevier: Oxford, Vol.
-
Pearson, W. H.; Lian, B. W.; Bergmeier, S. C. Aziridines and Azirines: Monocyclic. In Comprehensive Heterocyclic Chemistry II; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Elsevier: Oxford, 1996; Vol. 1A, p 8.
-
(1996)
Comprehensive Heterocyclic Chemistry II
, vol.1
, pp. 8
-
-
Pearson, W.H.1
Lian, B.W.2
Bergmeier, S.C.3
-
35
-
-
80051776167
-
-
Sun, X.; Worthy, A. D.; Tan, K. L. Angew. Chem., Int. Ed. 2011, 50, 8167-8171
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 8167-8171
-
-
Sun, X.1
Worthy, A.D.2
Tan, K.L.3
-
36
-
-
47749098988
-
-
Lightburn, T. E.; Dombrowski, M. T.; Tan, K. L. J. Am. Chem. Soc. 2008, 130, 9210-9211
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 9210-9211
-
-
Lightburn, T.E.1
Dombrowski, M.T.2
Tan, K.L.3
-
37
-
-
79961244115
-
-
Tan, K. L. ACS Catal. 2011, 1, 877-886
-
(2011)
ACS Catal.
, vol.1
, pp. 877-886
-
-
Tan, K.L.1
-
39
-
-
77954548753
-
-
Koohang, A.; Bailey, J. L.; Coates, R. M.; Erickson, H. K.; Owen, D.; Poulter, C. D. J. Org. Chem. 2010, 75, 4769-4777
-
(2010)
J. Org. Chem.
, vol.75
, pp. 4769-4777
-
-
Koohang, A.1
Bailey, J.L.2
Coates, R.M.3
Erickson, H.K.4
Owen, D.5
Poulter, C.D.6
-
40
-
-
15044358964
-
-
A very interesting case reported by the Somfai group documents α-tosylamino aldehyde with very similar connectivity.
-
A very interesting case reported by the Somfai group documents α-tosylamino aldehyde with very similar connectivity. Restorp, P.; Somfai, P. Org. Lett. 2005, 7, 893-895
-
(2005)
Org. Lett.
, vol.7
, pp. 893-895
-
-
Restorp, P.1
Somfai, P.2
-
41
-
-
0020630466
-
-
Pennings, M. L. M.; Reinhoudt, D. N.; Harkema, S.; Van Hummel, G. J. J. Org. Chem. 1983, 48, 486-491
-
(1983)
J. Org. Chem.
, vol.48
, pp. 486-491
-
-
Pennings, M.L.M.1
Reinhoudt, D.N.2
Harkema, S.3
Van Hummel, G.J.4
-
42
-
-
55949132381
-
-
He, M.; Beahm, B. J.; Bode, J. W. Org. Lett. 2008, 10, 3817-3820
-
(2008)
Org. Lett.
, vol.10
, pp. 3817-3820
-
-
He, M.1
Beahm, B.J.2
Bode, J.W.3
-
44
-
-
4143147497
-
-
Seki, M.; Hatsuda, M.; Yoshida, S.-I. Tetrahedron Lett. 2004, 45, 6579-6581
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 6579-6581
-
-
Seki, M.1
Hatsuda, M.2
Yoshida, S.-I.3
-
45
-
-
9644279789
-
-
Seki, M.; Hatsuda, M.; Mori, Y.; Yoshida, S.-I.; Yamada, S. I.; Shimizu, T. Chem.-Eur. J. 2004, 10, 6102-6110
-
(2004)
Chem.-Eur. J.
, vol.10
, pp. 6102-6110
-
-
Seki, M.1
Hatsuda, M.2
Mori, Y.3
Yoshida, S.-I.4
Yamada, S.I.5
Shimizu, T.6
-
46
-
-
44349161123
-
-
Ye, L.-W.; Zhou, J.; Tang, Y. Chem. Soc. Rev. 2008, 37, 1140-1152
-
(2008)
Chem. Soc. Rev.
, vol.37
, pp. 1140-1152
-
-
Ye, L.-W.1
Zhou, J.2
Tang, Y.3
-
49
-
-
33845701141
-
-
Bonini, B. F.; Capito, E.; Comes-Franchini, M.; Fochi, M.; Riccia, A.; Zwanenburg, B. Tetrahedron: Asymmetry 2006, 17, 3135-3143
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 3135-3143
-
-
Bonini, B.F.1
Capito, E.2
Comes-Franchini, M.3
Fochi, M.4
Riccia, A.5
Zwanenburg, B.6
-
51
-
-
77955586031
-
-
Chemoselectivepeptidomimetic ligation is the main application of the resulting diamine building blocks
-
Chemoselectivepeptidomimetic ligation is the main application of the resulting diamine building blocks: Assem, N.; Natarajan, A.; Yudin, A. K. J. Am. Chem. Soc. 2010, 132, 10986-10987
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 10986-10987
-
-
Assem, N.1
Natarajan, A.2
Yudin, A.K.3
-
52
-
-
0019588236
-
-
Cox, C.; Rinehart, K.; Moore, M.; Cook, J. Proc. Natl. Acad. Sci.-Biol. 1981, 78, 4256-4260
-
(1981)
Proc. Natl. Acad. Sci.-Biol.
, vol.78
, pp. 4256-4260
-
-
Cox, C.1
Rinehart, K.2
Moore, M.3
Cook, J.4
-
53
-
-
33845191735
-
-
a units in comparison to their corresponding amines. This ensures that the aniline Schiff base is significantly protonated compared to the oxime. The transamination of the more populated protonated aniline imine to the oxime is significantly faster than imine formation with a weakly protonated carbonyl group.
-
a units in comparison to their corresponding amines. This ensures that the aniline Schiff base is significantly protonated compared to the oxime. The transamination of the more populated protonated aniline imine to the oxime is significantly faster than imine formation with a weakly protonated carbonyl group.
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 7581-7584
-
-
Dirksen, A.1
Hackeng, T.M.2
Dawson, P.E.3
-
55
-
-
67849094631
-
-
Munos, J. W.; Pu, X.; Mansoorabadi, S. O.; Kim, H. J.; Liu, H.-W. J. Am. Chem. Soc. 2009, 131, 2048-2049
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 2048-2049
-
-
Munos, J.W.1
Pu, X.2
Mansoorabadi, S.O.3
Kim, H.J.4
Liu, H.-W.5
-
56
-
-
79951521008
-
-
Morten, C. J.; Byers, J. A.; Jamison, T. F. J. Am. Chem. Soc. 2011, 133, 1902-1908
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 1902-1908
-
-
Morten, C.J.1
Byers, J.A.2
Jamison, T.F.3
-
57
-
-
37049082787
-
-
Soai, K.; Niwa, S.; Hori, H. J. Chem. Soc., Chem. Commun. 1990, 982-983
-
(1990)
J. Chem. Soc., Chem. Commun.
, pp. 982-983
-
-
Soai, K.1
Niwa, S.2
Hori, H.3
-
58
-
-
0033623873
-
-
Soai, K.; Shibata, T.; Sato, I. Acc. Chem. Res. 2000, 33, 382-390
-
(2000)
Acc. Chem. Res.
, vol.33
, pp. 382-390
-
-
Soai, K.1
Shibata, T.2
Sato, I.3
-
61
-
-
34250883890
-
-
Collum, D. B.; McNeil, A. J.; Ramirez, A. Angew. Chem., Int. Ed. 2007, 46, 3002-3017
-
(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 3002-3017
-
-
Collum, D.B.1
McNeil, A.J.2
Ramirez, A.3
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