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1
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1642442463
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T. Bruckdorfer, O. Marder, F. Albericio, Current Pharm. Biotechnol. 2004, 5, 29-43.
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Current Pharm. Biotechnol.
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Bruckdorfer, T.1
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Albericio, F.3
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2
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67649274217
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A. Isidro-Llobet, M. Alvarez, F. Albericio, Chem. Rev. 2009, 109, 2455-2504.
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Chem. Rev.
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Isidro-Llobet, A.1
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Albericio, F.3
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3
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77953825940
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Eds.: J. Tulla-Puche, F. Albericio, Wiley-VCH, Weinheim, Germany
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J. Tulla-Puche, F. Albericio in The Power of Functional Resins in Organic Chemistry (Eds.: J. Tulla-Puche, F. Albericio), Wiley-VCH, Weinheim, Germany, 2008, pp. 495-527.
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(2008)
The Power of Functional Resins in Organic Chemistry
, pp. 495-527
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Tulla-Puche, J.1
Albericio, F.2
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4
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70350323495
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A. A. Zompra, A. S. Galanis, O. Werbitzky, F. Albericio, Future Med. Chem. 2009, 1, 361-377.
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(2009)
Future Med. Chem.
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Zompra, A.A.1
Galanis, A.S.2
Werbitzky, O.3
Albericio, F.4
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9
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0027441062
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L. A. Carpino, H. Shroff, S. A. Triolo, E.-S. M. E. Mansour, H. Wenschuh, F. Albericio, Tetrahedron Lett. 1993, 34, 7829-7832.
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(1993)
Tetrahedron Lett.
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Carpino, L.A.1
Shroff, H.2
Triolo, S.A.3
Mansour, E.-S.M.E.4
Wenschuh, H.5
Albericio, F.6
-
10
-
-
77953817528
-
-
The abbreviations used are derived from the Pmc and Pbf groups used for Arg protecting groups by adding an "m", which represent the methyl moiety
-
The abbreviations used are derived from the Pmc and Pbf groups used for Arg protecting groups by adding an "m", which represent the methyl moiety.
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11
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0038684450
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O. García, E. Nicolás, F. Albericio, Tetrahedron Lett. 2003, 44, 5319-5321.
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Tetrahedron Lett.
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García, O.1
Nicolás, E.2
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12
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84981754168
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H. Gross, A. Rieche, G. Mattey, Chem. Ber. 1963, 96, 308-319.
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Chem. Ber.
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Gross, H.1
Rieche, A.2
Mattey, G.3
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14
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0025032015
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F. Albericio, N. Kneib-Cordonier, S. Biancalana, L. Gera, R. I. Masada, D. Hudson, G. Barany, J. Org. Chem. 1990, 55, 3730-3743.
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J. Org. Chem.
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Albericio, F.1
Kneib-Cordonier, N.2
Biancalana, S.3
Gera, L.4
Masada, R.I.5
Hudson, D.6
Barany, G.7
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16
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0000836350
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C. García-Echeverría, F. Albericio, M. Pons, G. Barany, E. Giralt, Tetrahedron Lett. 1989, 30, 2441-2444.
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(1989)
Tetrahedron Lett.
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García-Echeverría, C.1
Albericio, F.2
Pons, M.3
Barany, G.4
Giralt, E.5
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17
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-
77953854517
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K. Barlos, D. Gatos, S. Kutsogianni, G. Papaphotiou, C. Poulos, T. Tsegenidis, Int. J. Peptide Prot. Res. 1991, 38, 562568.
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(1991)
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Barlos, K.1
Gatos, D.2
Kutsogianni, S.3
Papaphotiou, G.4
Poulos, C.5
Tsegenidis, T.6
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18
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77953841515
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-
All attempts to prepare halogeno and tosyl derivatives were not successful at all.
-
All attempts to prepare halogeno and tosyl derivatives were not successful at all.
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-
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19
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4243553426
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a) A.D. Becke, Phys. Rev. 1988, A38, 3098-3100;
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Phys. Rev.
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Becke, A.D.1
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22
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0004133516
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Gaussian, Inc., Pittsburgh, PA
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d) M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, V. G. Zakrzewski, J. A. Montgomery, R. E. Stratmann Jr., J. C. Burant, S. Dapprich, J. M. Millam, A. D. Daniels, K. N. Kudin, M. C. Strain, O. Parkas, J. Tomasi, V. Barone, M. Cossi, R. Cammi, B. Mennucci, C. Pomelli, C. Adamo, S. Clifford, J. Ochterski, G. A. Petersson, P. Y. Ayala, Q. Cui, K. Morokuma, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. Cioslowski, J. V. Ortiz, B. B. Stefanov, G. Lin, A. Liashenko, P. Piskorz, I. Komaromi, R. Gomperts, R. L. Martin, D. J. Fox, T. Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, C. Gonzalez, M. Challacombe P. M. W. Gill, B. G. Johnson, W. Chen, M. W. Wong, J. L. Andres, M. HeadGordon, E. S. Replogle, J. A. Pople, Gaussian 98, revision A.9, Gaussian, Inc., Pittsburgh, PA, 1998.
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(1998)
Gaussian 98, Revision A.9
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Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Zakrzewski, V.G.7
Montgomery, J.A.8
Stratmann Jr., R.E.9
Burant, J.C.10
Dapprich, S.11
Millam, J.M.12
Daniels, A.D.13
Kudin, K.N.14
Strain, M.C.15
Parkas, O.16
Tomasi, J.17
Barone, V.18
Cossi, M.19
Cammi, R.20
Mennucci, B.21
Pomelli, C.22
Adamo, C.23
Clifford, S.24
Ochterski, J.25
Petersson, G.A.26
Ayala, P.Y.27
Cui, Q.28
Morokuma, K.29
Malick, D.K.30
Rabuck, A.D.31
Raghavachari, K.32
Foresman, J.B.33
Cioslowski, J.34
Ortiz, J.V.35
Stefanov, B.B.36
Lin, G.37
Liashenko, A.38
Piskorz, P.39
Komaromi, I.40
Gomperts, R.41
Martin, R.L.42
Fox, D.J.43
Keith, T.44
Al-Laham, M.A.45
Peng, C.Y.46
Nanayakkara, A.47
Gonzalez, C.48
Challacombe, M.49
Gill, P.M.W.50
Johnson, B.G.51
Chen, W.52
Wong, M.W.53
Andres, J.L.54
HeadGordon, M.55
Replogle, E.S.56
Pople, J.A.57
more..
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23
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84946893847
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a) J. Tomasi, S. Miertus, E. Scrocco, J. Chem. Phys. 1981, 114, 117-129;
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Tomasi, J.1
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84962359221
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c) M. Cossi, V. Barone, R. Cammi, J. Tomasi, Chem. Phys. Lett. 1996, 255, 327-335;
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Cossi, M.1
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27
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2542510395
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H. M. S. Kumar, B. V. S. Reddy, P. T. Reddy, J. S. Yadav, Synthesis 1999, 586-587.
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Synthesis
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Kumar, H.M.S.1
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Yadav, J.S.4
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28
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77953823117
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Yields were not optimized.
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Yields were not optimized.
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