-
2
-
-
0034678033
-
-
S. L. Schreiber, Science 2000, 287, 1964-1969.
-
(2000)
Science
, vol.287
, pp. 1964-1969
-
-
Schreiber, S.L.1
-
3
-
-
0037366605
-
-
D. A. Horton, G. T. Bourne, M. L. Smythe, Chem. Rev. 2003, 103, 893-930.
-
(2003)
Chem. Rev.
, vol.103
, pp. 893-930
-
-
Horton, D.A.1
Bourne, G.T.2
Smythe, M.L.3
-
4
-
-
4644244117
-
-
For a selection of recent examples see: a) O. Müller, E. Gourzoulidou, M. Carpintero, I. -M. Karaguni, A. Langerak, C. Herrmann, T. Möröy, L. Klein-Hitpaß, H. Waldmann, Angew. Chem. 2004, 116, 456-460;
-
(2004)
Angew. Chem.
, vol.116
, pp. 456-460
-
-
Müller, O.1
Gourzoulidou, E.2
Carpintero, M.3
Karaguni, I.M.4
Langerak, A.5
Herrmann, C.6
Möröy, T.7
Klein-Hitpaß, L.8
Waldmann, H.9
-
6
-
-
10744221485
-
-
b) L. T. Vassilev, B. T. Vu, B. Graves, D. Carvajal, E. Podlaski, Z. Filipovic, N. Kong, U. Kammlott, C. Lukacs, C. Klein, N. Fotouhi, E. A. Liu, Science 2004, 303, 844-848;
-
(2004)
Science
, vol.303
, pp. 844-848
-
-
Vassilev, L.T.1
Vu, B.T.2
Graves, B.3
Carvajal, D.4
Podlaski, E.5
Filipovic, Z.6
Kong, N.7
Kammlott, U.8
Lukacs, C.9
Klein, C.10
Fotouhi, N.11
Liu, E.A.12
-
7
-
-
0037061492
-
-
c) F. G. Kuruvilla, A. F. Shamji, S. M. Sternson, P. J. Hergenrother, S. L. Schreiber. Nature 2002, 416, 653-657.
-
(2002)
Nature
, vol.416
, pp. 653-657
-
-
Kuruvilla, F.G.1
Shamji, A.F.2
Sternson, S.M.3
Hergenrother, P.J.4
Schreiber, S.L.5
-
11
-
-
0030036459
-
-
a) Demethoxyfumitremorgin C and tryprostatins: C.B. Cui, H. Kakeya, H. Osada, J. Antibiot. 1996, 49, 534-540;
-
(1996)
J. Antibiot.
, vol.49
, pp. 534-540
-
-
Cui, C.B.1
Kakeya, H.2
Osada, H.3
-
13
-
-
4344649583
-
-
c) Roquefortine C: D. J. Richard, B. Schiavi, M. M. Joullie, Proc. Natl. Acad. Sci. USA 2004, 101, 11971-11976;
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 11971-11976
-
-
Richard, D.J.1
Schiavi, B.2
Joullie, M.M.3
-
14
-
-
4344716608
-
-
d) Rosstratins: R. X. Tan, P. R. Jensen, P. G. Williams, W. Fenical, J. Nat. Prod. 2004, 67, 1374-1382;
-
(2004)
J. Nat. Prod.
, vol.67
, pp. 1374-1382
-
-
Tan, R.X.1
Jensen, P.R.2
Williams, P.G.3
Fenical, W.4
-
15
-
-
20444482427
-
-
e) Vertihemiptellides: M. Isaka, S. Palasarn, P. Rachtawee, S. Vimuttipong, P. Kongsaeree, Org. Lett. 2005, 7, 2257-2260.
-
(2005)
Org. Lett.
, vol.7
, pp. 2257-2260
-
-
Isaka, M.1
Palasarn, S.2
Rachtawee, P.3
Vimuttipong, S.4
Kongsaeree, P.5
-
16
-
-
27444444293
-
-
Selected examples of biologically active DKPs: a) Oxytocin antagonists: A. D. Borthwick, D. E. Davies, A. -M. Exall, D. G. Livermore, S. L. Sollis, F. Nerozzi, M. J. Allen, M. Perren, S. S. Shabbir, P. M. Woollard, P.G. Wyatt, J. Med. Chem. 2005, 48, 6956-6969;
-
(2005)
J. Med. Chem.
, vol.48
, pp. 6956-6969
-
-
Borthwick, A.D.1
Davies, D.E.2
Exall, A.M.3
Livermore, D.G.4
Sollis, S.L.5
Nerozzi, F.6
Allen, M.J.7
Perren, M.8
Shabbir, S.S.9
Woollard, P.M.10
Wyatt, P.G.11
-
17
-
-
33646118484
-
-
b) tubulin polymerizing agents with antitumour activity: B. Nicholson. G. K. Lloyd, B. R. Miller, M. A. Palladino, Y. Kiso, Y. Hayashi, S. T. Neuteboom, Anti-cancer Drug 2006, 7, 25-31;
-
(2006)
Anti-cancer Drug
, vol.7
, pp. 25-31
-
-
Nicholson, B.1
Lloyd, G.K.2
Miller, B.R.3
Palladino, M.A.4
Kiso, Y.5
Hayashi, Y.6
Neuteboom, S.T.7
-
18
-
-
23444442242
-
-
c) neuroprotective activity: A. I. Faden, V. A. Movsesyan, S. M. Knoblach, F. Ahmed, I. Cernak, Neuropharmacology 2005, 49, 410-424;
-
(2005)
Neuropharmacology
, vol.49
, pp. 410-424
-
-
Faden, A.I.1
Movsesyan, V.A.2
Knoblach, S.M.3
Ahmed, F.4
Cernak, I.5
-
19
-
-
4344692277
-
-
d) Inhibitor of plasminogen activator inhibitor (PAI)-1 activity: T. D. Brooks, S.W. Wang, N. Brunner, P. A. Charlton, Anti-cancer Drugs 2004, 15, 37-44;
-
(2004)
Anti-cancer Drugs
, vol.15
, pp. 37-44
-
-
Brooks, T.D.1
Wang, S.W.2
Brunner, N.3
Charlton, P.A.4
-
20
-
-
14644431688
-
-
e) tryptase inhibitors: M. del Fresno, D. Fernandez-Forner, M. Miralpeix, V. Segarra, H. Ryder, M. Royo, F. Albericio, Bioorg. Med. Chem. Lett. 2005, 15, 1659-1664.
-
(2005)
Bioorg. Med. Chem. Lett.
, vol.15
, pp. 1659-1664
-
-
Del Fresno, M.1
Fernandez-Forner, D.2
Miralpeix, M.3
Segarra, V.4
Ryder, H.5
Royo, M.6
Albericio, F.7
-
22
-
-
20344397439
-
-
For use of Ugi reactions see: S. L. Sollis, J. Org. Chem. 2005, 70, 4735-4740.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 4735-4740
-
-
Sollis, S.L.1
-
23
-
-
0345871009
-
-
S. Cho, G. Keum, S. B. Kang, S. Y. Han, Y. Kim, Mol. Diversity 2003, 6. 283-286.
-
(2003)
Mol. Diversity
, vol.6
, pp. 283-286
-
-
Cho, S.1
Keum, G.2
Kang, S.B.3
Han, S.Y.4
Kim, Y.5
-
24
-
-
0000585031
-
-
Cyclic N-acyliminium ions derived from peptide aldehydes are powerful intermediates that can undergo intramolecular attack by a range of nucleophiles including amide backbone NH and side chain functional groups (for example, hydroxyl, sulfhydryl, amide, amide groups, and carbon-based π-nucleophiles) to generate bicyclic scaffolds with ring structure diversity. For general solid-phase synthesis approaches see; a) T. Vojkovsky, A. Weichsel, M. Patek, J. Org. Chem. 1998, 63, 3162-3163;
-
(1998)
J. Org. Chem.
, vol.63
, pp. 3162-3163
-
-
Vojkovsky, T.1
Weichsel, A.2
Patek, M.3
-
27
-
-
0033602269
-
-
P. Johannesson, G. Lindeberg, W. Tong, A. Gogoll, A. Karlen, A. Hallberg, J. Med. Chem. 1999, 42, 601-608;
-
(1999)
J. Med. Chem.
, vol.42
, pp. 601-608
-
-
Johannesson, P.1
Lindeberg, G.2
Tong, W.3
Gogoll, A.4
Karlen, A.5
Hallberg, A.6
-
28
-
-
0033616089
-
-
d) M. Eguchi, M. S. Lee, H. Nakanishi, M. Stasiak, S. Lovell, M. Kahn, J. Am. Chem. Soc. 1999, 121, 12204-12205;
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 12204-12205
-
-
Eguchi, M.1
Lee, M.S.2
Nakanishi, H.3
Stasiak, M.4
Lovell, S.5
Kahn, M.6
-
29
-
-
14844357298
-
-
e) T.E. Nielsen, S. Le Quement, M. Meldal, Org. Lett. 2005, 7, 581-584.
-
(2005)
Org. Lett.
, vol.7
, pp. 581-584
-
-
Nielsen, T.E.1
Le Quement, S.2
Meldal, M.3
-
30
-
-
0031767227
-
-
3THF have been proposed as templates for the elaboration of various heterocyclic scaffolds, a) J. M. Ostresh, C. C. Schoner, V. T. Hamashin, A. Nefzi, J. P. Meyer, R. A. Houghten, J. Org. Chem., 1998, 63, 8622-8623;
-
(1998)
J. Org. Chem.
, vol.63
, pp. 8622-8623
-
-
Ostresh, J.M.1
Schoner, C.C.2
Hamashin, V.T.3
Nefzi, A.4
Meyer, J.P.5
Houghten, R.A.6
-
31
-
-
2442711475
-
-
and references therein
-
b) A. Nefzi, J. M. Ostresh, J. Yu, R. A. Houghten, J. Org. Chem. 2004, 69, 3603-3609, and references therein;
-
(2004)
J. Org. Chem.
, vol.69
, pp. 3603-3609
-
-
Nefzi, A.1
Ostresh, J.M.2
Yu, J.3
Houghten, R.A.4
-
33
-
-
31544475482
-
-
d) C. E. Hoesl, J. M. Ostresh, R. A. Houghten, A. Nefzi, J. Comb. Chem. 2006, 8, 127-131.
-
(2006)
J. Comb. Chem.
, vol.8
, pp. 127-131
-
-
Hoesl, C.E.1
Ostresh, J.M.2
Houghten, R.A.3
Nefzi, A.4
-
35
-
-
0037347908
-
-
a) 1,4-Diazepan-2,5-diones: J. C. D. Müller-Hartwieg, K. G. Akyel. J. Zimmermann, J. Pept. Sci. 2003, 9, 187-199;
-
(2003)
J. Pept. Sci.
, vol.9
, pp. 187-199
-
-
Müller-Hartwieg, J.C.D.1
Akyel, K.G.2
Zimmermann, J.3
-
36
-
-
0033978526
-
-
O. El Mahdi, J. P. Lavergne, J. Martinez, P. Viallefont, E. M. Essassi, C. Riche, Eur. J. Org. Chem. 2000, 251-255;
-
(2000)
Eur. J. Org. Chem.
, pp. 251-255
-
-
El Mahdi, O.1
Lavergne, J.P.2
Martinez, J.3
Viallefont, P.4
Essassi, E.M.5
Riche, C.6
-
37
-
-
0030062497
-
-
b) 1,2,5-triazepan-3,6-diones: M. M. Lenman, S. L. Ingham, D. Gani, Chem. Commun. 1996, 85-87;
-
(1996)
Chem. Commun.
, pp. 85-87
-
-
Lenman, M.M.1
Ingham, S.L.2
Gani, D.3
-
39
-
-
0028057975
-
-
a) Containing a 1,3-diazepan-2-one skeleton; P. Y. Lam, P. K. Jadhav, C. J. Eyermann, C. N. Hodge, Y. Ru, L. T. Bacheler, J. L. Meek, M. J. Otto, M. M. Rayner, Y. N. Wong, C. H. Chang, P. C. Wever, D. A. Jackson, T. R. Sharpe, S. Erickson-Vitanen, Science 1994, 263, 380-384;
-
(1994)
Science
, vol.263
, pp. 380-384
-
-
Lam, P.Y.1
Jadhav, P.K.2
Eyermann, C.J.3
Hodge, C.N.4
Ru, Y.5
Bacheler, L.T.6
Meek, J.L.7
Otto, M.J.8
Rayner, M.M.9
Wong, Y.N.10
Chang, C.H.11
Wever, P.C.12
Jackson, D.A.13
Sharpe, T.R.14
Erickson-Vitanen, S.15
-
40
-
-
13344295092
-
-
b) containing a 1,2,4-triazepan-3-one skeleton: H. L. Sham, C. Zhao, K. D. Stewart, D. A. Betebenner, S. Lin, C. H. Park, X. -P. Kong, W. Jr., Rosenbrook, T. Herrin, D. Madigan, S. Vasavanonda, N. Lyons, A. Molla, A. Saldivar, K. C. Marsh, E. McDonald, N. E. Wideburg, J. F. Denissen, T. Robins, D. J. Kempf, J. J. Plattner, D. W. Norbeck, J. Med. Chem. 1996, 39, 392-397.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 392-397
-
-
Sham, H.L.1
Zhao, C.2
Stewart, K.D.3
Betebenner, D.A.4
Lin, S.5
Park, C.H.6
Kong, X.P.7
Rosenbrook Jr., W.8
Herrin, T.9
Madigan, D.10
Vasavanonda, S.11
Lyons, N.12
Molla, A.13
Saldivar, A.14
Marsh, K.C.15
McDonald, E.16
Wideburg, N.E.17
Denissen, J.F.18
Robins, T.19
Kempf, D.J.20
Plattner, J.J.21
Norbeck, D.W.22
more..
-
42
-
-
33751307631
-
-
Chem. Abstr. 2001 134, 237502.
-
(2001)
Chem. Abstr.
, vol.134
, pp. 237502
-
-
-
43
-
-
0032491225
-
-
R. A. Galemmo Jr, T. P. Maduskuie, C. Dominguez, K. A. Rossi, R. M. Knabb, R. R. Wexlcr, P. F. Stouten, Bioorg. Med. Chem. Lett. 1998, 8, 2705-2710.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 2705-2710
-
-
Galemmo Jr., R.A.1
Maduskuie, T.P.2
Dominguez, C.3
Rossi, K.A.4
Knabb, R.M.5
Wexlcr, R.R.6
Stouten, P.F.7
-
44
-
-
4444347175
-
-
A. Bonnefoy, C. Dupuis-Hamelin, V. Steier, C. Delachaume, C. Seys, T. Stachyra, M. Fairley, M. Guitton, M. Lampilas, J. Antimicrob. Chemother. 2004, 54, 410-417.
-
(2004)
J. Antimicrob. Chemother.
, vol.54
, pp. 410-417
-
-
Bonnefoy, A.1
Dupuis-Hamelin, C.2
Steier, V.3
Delachaume, C.4
Seys, C.5
Stachyra, T.6
Fairley, M.7
Guitton, M.8
Lampilas, M.9
-
45
-
-
0034725731
-
-
S. F. Martin, B. C. Follows, P. J. Hergenrother, C. L. Franklin, J. Org. Chem. 2000, 65, 4509-4514.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 4509-4514
-
-
Martin, S.F.1
Follows, B.C.2
Hergenrother, P.J.3
Franklin, C.L.4
-
46
-
-
33751337741
-
-
WO 2004092169
-
R. Nishizawa, Y. Takaoka, H. Habashita, S. Shibayama, M. Kokubo, WO 2004092169, 2004;
-
(2004)
-
-
Nishizawa, R.1
Takaoka, Y.2
Habashita, H.3
Shibayama, S.4
Kokubo, M.5
-
47
-
-
33751351631
-
-
[Chem. Abstr. 2004 141, 395 591].
-
(2004)
Chem. Abstr.
, vol.141
-
-
-
48
-
-
0017878930
-
-
To our knowledge, seven triazepandione systems out of 16 possible isomers have been reported so far in the literature, a) 1,2,4-Triazepan-3,5-dione; A. Hasnaoui, J. -P. Lavergne, P. Viallefont, J. Heterocycl. Chem. 1978, 15, 71-75;
-
(1978)
J. Heterocycl. Chem.
, vol.15
, pp. 71-75
-
-
Hasnaoui, A.1
Lavergne, J.P.2
Viallefont, P.3
-
49
-
-
33751348515
-
-
WO 9422840
-
b) 1,2,4-triazepan-3,7-dione: C.N. Hodge, C.H. Fernandez, P. K. Jadhav, P. Y. Lam, WO 9422840, 1994;
-
(1994)
-
-
Hodge, C.N.1
Fernandez, C.H.2
Jadhav, P.K.3
Lam, P.Y.4
-
50
-
-
0005533943
-
-
[Chem. Abs. 1994, 123, 33104];
-
(1994)
Chem. Abs.
, vol.123
, pp. 33104
-
-
-
51
-
-
0031006932
-
-
c) 1,2,5-triazepan-3,4-dione: A.M.M. El-Saghier, A.A. Maihub, H. Al-Shirayda, Synth. Commun. 1997, 27, 2433-2444;
-
(1997)
Synth. Commun.
, vol.27
, pp. 2433-2444
-
-
El-Saghier, A.M.M.1
Maihub, A.A.2
Al-Shirayda, H.3
-
52
-
-
33751345551
-
-
1,2,5-triazepan-3,6-dione: see reference [11b]
-
d) 1,2,5-triazepan-3,6-dione: see reference [11b];
-
-
-
-
53
-
-
33751343884
-
-
EP 172552
-
e) 1,2,5-triazepan-3,7-dione: C. Hassal, G. Lawon, S. Radshaw, EP 172552, 1986;
-
(1986)
-
-
Hassal, C.1
Lawon, G.2
Radshaw, S.3
-
54
-
-
33751330896
-
-
[Chem. Abs. 1986, 105, 115 100];
-
(1986)
Chem. Abs.
, vol.105
-
-
-
55
-
-
0029591753
-
-
f) 1,3,5-triazepan-2,4-dione: H. Sawanishi, S. Wakusawa, R. Murakami, H. Muramatsu, H. Suzuki, A. Takashima, T. Aizawa, K. -I. Miyamoto, J. Med. Chem. 1995, 38, 5066-5070;
-
(1995)
J. Med. Chem.
, vol.38
, pp. 5066-5070
-
-
Sawanishi, H.1
Wakusawa, S.2
Murakami, R.3
Muramatsu, H.4
Suzuki, H.5
Takashima, A.6
Aizawa, T.7
Miyamoto, K.I.8
-
56
-
-
0035817979
-
-
T. Yu, J. M. Ostresh, R. A. Houghten, Org. Lett. 2001, 3, 2797-2799;
-
(2001)
Org. Lett.
, vol.3
, pp. 2797-2799
-
-
Yu, T.1
Ostresh, J.M.2
Houghten, R.A.3
-
57
-
-
37049103025
-
-
g) 1,3,5-triazepan-2,7-dione: K. Hirota, K. Maruhashi, N. Kitamura, T. Asao, S. Senda, J. Chem. Soc. Perkin Trans, 1 1984, 1719-1723.
-
(1984)
J. Chem. Soc. Perkin Trans, 1
, pp. 1719-1723
-
-
Hirota, K.1
Maruhashi, K.2
Kitamura, N.3
Asao, T.4
Senda, S.5
-
58
-
-
0000845126
-
-
We use a nomenclature based on the amino acid three letter code to describe 1,3,5-triazepan-2,6-diones. Accordingly, heterocycles prepared from the dipeptide sequence Boc-Xaa-Xbb-OH will be denoted cyclo(Xaa-gXbb-CO). g = gem, refers to the 2-alkyl gem-diamino-derivative of the corresponding amino acid according to the nomenclature proposed by Goodman. M. Chorev, M. Goodman, Acc. Chem. Res. 1993, 26, 266-273.
-
(1993)
Acc. Chem. Res.
, vol.26
, pp. 266-273
-
-
Chorev, M.1
Goodman, M.2
-
59
-
-
0012432084
-
-
V. Semetey, C. Didierjean, J. -P. Briand, A. Aubry, G. Guichard. Angew. Chem. 2002, 114, 1975-1978
-
(2002)
Angew. Chem.
, vol.114
, pp. 1975-1978
-
-
Semetey, V.1
Didierjean, C.2
Briand, J.P.3
Aubry, A.4
Guichard, G.5
-
60
-
-
0037013980
-
-
: Angew. Chem. Int. Ed. 2002, 41, 1895-1898.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 1895-1898
-
-
-
61
-
-
0033550306
-
-
a) G. Guichard, V. Semetey, C. Didierjean, A. Aubry, J. P. Briand, M. Rodriguez, J. Org. Chem. 1999, 64, 8702-8705;
-
(1999)
J. Org. Chem.
, vol.64
, pp. 8702-8705
-
-
Guichard, G.1
Semetey, V.2
Didierjean, C.3
Aubry, A.4
Briand, J.P.5
Rodriguez, M.6
-
62
-
-
0035969628
-
-
b) V. Semetey, D. Rognan, C. Hemmerlin, C. Didierjean, A. -P. Schaffner, A. Gimenez Giner, A. Aubry, J. -P. Briand, M. Marraud, G. Guichard, Org. Lett. 2001, 3, 3843-3846.
-
(2001)
Org. Lett.
, vol.3
, pp. 3843-3846
-
-
Semetey, V.1
Rognan, D.2
Hemmerlin, C.3
Didierjean, C.4
Schaffner, A.P.5
Gimenez Giner, A.6
Aubry, A.7
Briand, J.P.8
Marraud, M.9
Guichard, G.10
-
63
-
-
33751307882
-
-
2O and filtration
-
2O and filtration.
-
-
-
-
65
-
-
0000613918
-
-
Chapters 3.2 and 3.3 in C. C. Tzschucke, C. Markert, W. Bannwarth, S. Roller, A. Hebel, R. Haag, Angew. Chem. 2002, 114, 4136-4173;
-
(2002)
Angew. Chem.
, vol.114
, pp. 4136-4173
-
-
Tzschucke, C.C.1
Markert, C.2
Bannwarth, W.3
Roller, S.4
Hebel, A.5
Haag, R.6
-
66
-
-
0037021091
-
-
Angew. Chem. Int. Ed. 2002, 41, 3964-4000.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 3964-4000
-
-
-
67
-
-
0033556116
-
-
M. Adamczyk, J. R. Fishpaugh, P. G. Mattingly, Tetrahedron Lett. 1999, 40, 463-466.
-
(1999)
Tetrahedron Lett.
, vol.40
, pp. 463-466
-
-
Adamczyk, M.1
Fishpaugh, J.R.2
Mattingly, P.G.3
-
68
-
-
0015520853
-
-
T. Shioiri, K. Ninomiya, S. Yamada, J. Am. Chem. Soc. 1972, 94, 6203-6205.
-
(1972)
J. Am. Chem. Soc.
, vol.94
, pp. 6203-6205
-
-
Shioiri, T.1
Ninomiya, K.2
Yamada, S.3
-
69
-
-
14444287797
-
-
a) D. A. Nugiel, K. Jacobs, L. Cornelius, C. -H. Chang, P. K. Jadhav, E. R. Holler, R. M. Klabe, L. T. Bacheler, B. Cordova, S. Garber, C. Reid, K. A. Logue, L. J. Gorey-Feret, G. N. Lam, S. Erickson-Viitanen, S. P. Seitz, J. Med. Chem. 1997, 40, 1465-1474;
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1465-1474
-
-
Nugiel, D.A.1
Jacobs, K.2
Cornelius, L.3
Chang, C.H.4
Jadhav, P.K.5
Holler, E.R.6
Klabe, R.M.7
Bacheler, L.T.8
Cordova, B.9
Garber, S.10
Reid, C.11
Logue, K.A.12
Gorey-Feret, L.J.13
Lam, G.N.14
Erickson-Viitanen, S.15
Seitz, S.P.16
-
70
-
-
15644376141
-
-
b) J. Hultén, N. M. Bonham, U. Nillroth, T. Hansson, G. Zucarello, A. Bouzide, J. Aqvist, J., B. Classon, U. H. Danielson, A. Karlen, I. Kvarnström, B. Samuelsson, A. Hallberg, J. Med. Chem. 1997, 40, 885-897.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 885-897
-
-
Hultén, J.1
Bonham, N.M.2
Nillroth, U.3
Hansson, T.4
Zucarello, G.5
Bouzide, A.6
Aqvist, J.7
Classon, B.8
Danielson, U.H.9
Karlen, A.10
Kvarnström, I.11
Samuelsson, B.12
Hallberg, A.13
-
71
-
-
9544235162
-
-
P. Y. S. Lam, Y. Ru, P. K. Jadhav, P. E. Aldrich, G. V. DeLucca, C. J. Eyermann, C. -H. Chang, G. Emett, E. R. Holler, W. F. Danedker, L. Li, P. N. Confalone, R. J. McHugh, Q. Han, R. Li, J. A. Markwalder, S. P. Seitz, T. R. Sharpe, L. T. Bacheler, M. M. Rayner, R. M. Klabe, L. Shum, D. L. Winslow, D. M. Kornhauser, D. A. Jackson, S. Erickson-Viitanen, C. N. Hodge, J. Med. Chem. 1996, 39, 3514-3525.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 3514-3525
-
-
Lam, P.Y.S.1
Ru, Y.2
Jadhav, P.K.3
Aldrich, P.E.4
Delucca, G.V.5
Eyermann, C.J.6
Chang, C.H.7
Emett, G.8
Holler, E.R.9
Danedker, W.F.10
Li, L.11
Confalone, P.N.12
McHugh, R.J.13
Han, Q.14
Li, R.15
Markwalder, J.A.16
Seitz, S.P.17
Sharpe, T.R.18
Bacheler, L.T.19
Rayner, M.M.20
Klabe, R.M.21
Shum, L.22
Winslow, D.L.23
Kornhauser, D.M.24
Jackson, D.A.25
Erickson-Viitanen, S.26
Hodge, C.N.27
more..
-
72
-
-
0031443171
-
-
W. W. Wilkerson, S. Dax, W. W. Cheatham, J. Med. Chem. 1997, 40, 4079-4088.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 4079-4088
-
-
Wilkerson, W.W.1
Dax, S.2
Cheatham, W.W.3
-
73
-
-
0032552205
-
-
B. R. P. Stone, G. D. Harris, R. O. Cann, T. E. Smyser and P. N. Confalone, Tetrahedron Lett. 1998, 39, 6127-6130.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 6127-6130
-
-
Stone, B.R.P.1
Harris, G.D.2
Cann, R.O.3
Smyser, T.E.4
Confalone, P.N.5
-
74
-
-
0028911233
-
-
N. A. Meanwell, S. Y. Sit, J. Gao, H. S. Wong, Q. Gao, D. R. St. Laurent, N. Balasubramanian, J. Org. Chem. 1995, 60, 1565-1582.
-
(1995)
J. Org. Chem.
, vol.60
, pp. 1565-1582
-
-
Meanwell, N.A.1
Sit, S.Y.2
Gao, J.3
Wong, H.S.4
Gao, Q.5
St. Laurent, D.R.6
Balasubramanian, N.7
-
75
-
-
0037064602
-
-
3 in organic synthesis see: B. E. Blass, Tetrahedron 2002, 58, 9301-9320.
-
(2002)
Tetrahedron
, vol.58
, pp. 9301-9320
-
-
Blass, B.E.1
-
76
-
-
33751315492
-
-
note
-
Quantitative removal of protecting groups in 9 and 11 by treatment with TFA afforded an additional set of triazepandiones with free carboxylic side chains (12 and 13, respectively).
-
-
-
-
77
-
-
33751318436
-
-
CCDC-283640 to -28346 contain the crystal structures of 4J, 4k, 4l, 4o, 4s, 9i, and 11c. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam. ac.uk/data_request/cif.
-
-
-
-
78
-
-
33644779614
-
-
For a structure report of 4h see: G. Lena, E. Wenger, G. Guichard, C. Didierjean, Acta Crystallogr. Sect. E 2006, 62, O518-O520.
-
(2006)
Acta Crystallogr. Sect. E
, vol.62
-
-
Lena, G.1
Wenger, E.2
Guichard, G.3
Didierjean, C.4
-
79
-
-
0004150157
-
-
University of Göttingen, Göttingen, Germany
-
During the crystallographic refinements, all H atoms were placed in calculated positions and refined by using a riding model, with C-H distances 0.93-0.98 Å and an N-H distance of 0.86 Å. G. M. Shel-drick, SHELXL-97, University of Göttingen, Göttingen, Germany, 1997.
-
(1997)
SHELXL-97
-
-
Sheldrick, G.M.1
-
80
-
-
0039686531
-
-
and references therein
-
See Table IV in: I. L, Karle, H. C. Ottenheym, B. Witkop, J. Am. Chem. Soc. 1974, 96, 539-543 and references therein.
-
(1974)
J. Am. Chem. Soc.
, vol.96
, pp. 539-543
-
-
Karle, I.L.1
Ottenheym, H.C.2
Witkop, B.3
-
83
-
-
33749525540
-
-
DOI: 10.1039/B604747E
-
2)8 dimers and can eventually pack into H-bonded molecular tapes. In the solid state, cyclo(L-Phe-gSar-CO) (4 a) was found to form H-bonded helicoidal molecular tapes with P chirality that self-assemble to give hollow tubular structures. A. P. Schaffner, G. Lena, S. Roussel, A. Aubry, J.-P. Briand, C. Didierjean, G. Guichard, Chem. Commun., DOI: 10.1039/B604747E.
-
Chem. Commun.
-
-
Schaffner, A.P.1
Lena, G.2
Roussel, S.3
Aubry, A.4
Briand, J.-P.5
Didierjean, C.6
Guichard, G.7
-
84
-
-
0346705252
-
-
For recent reviews on antimalarial drugs see: a) J. Wiesner, R. Ortmann, H. Jomaa, M. Schlitzer, Angew. Chem. 2003, 115, 5432-5451;
-
(2003)
Angew. Chem.
, vol.115
, pp. 5432-5451
-
-
Wiesner, J.1
Ortmann, R.2
Jomaa, H.3
Schlitzer, M.4
-
85
-
-
0344875966
-
-
Angew. Chem. Int. Ed., 2003, 42, 5274-5293;
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 5274-5293
-
-
-
86
-
-
85084849417
-
-
b) A. -C. Labbé, M. R. Loufty, K. C. Kain, Curr. Inf. Dis. Rep. 2001, 3, 68-76.
-
(2001)
Curr. Inf. Dis. Rep.
, vol.3
, pp. 68-76
-
-
Labbé, A.C.1
Loufty, M.R.2
Kain, K.C.3
-
87
-
-
33751328012
-
-
note
-
-1, see Supporting Information).
-
-
-
-
88
-
-
0021964206
-
-
D. Mazier, R. L. Beaudoin, S. Mellouk, P. Druilhe, B. Texier, J. Trosper, F. Miltgen, I. Landau, C. Paul, O. Brandicourt, C. Guguen-guillouzo, P. Langlois, M. Gentilini, Science 1985, 227, 440-442.
-
(1985)
Science
, vol.227
, pp. 440-442
-
-
Mazier, D.1
Beaudoin, R.L.2
Mellouk, S.3
Druilhe, P.4
Texier, B.5
Trosper, J.6
Miltgen, F.7
Landau, I.8
Paul, C.9
Brandicourt, O.10
Guguen-Guillouzo, C.11
Langlois, P.12
Gentilini, M.13
-
90
-
-
0025363462
-
-
L. Renia, D. M. Mattei, J. Goma, S. Pied, P. Dubois, F. Miltgen, A. K. Nussler, H. Matile, F. Menegaux, M. Gentilini, D. Mazier, Eur. J. Immunol. 1990, 20, 1445-1449.
-
(1990)
Eur. J. Immunol.
, vol.20
, pp. 1445-1449
-
-
Renia, L.1
Mattei, D.M.2
Goma, J.3
Pied, S.4
Dubois, P.5
Miltgen, F.6
Nussler, A.K.7
Matile, H.8
Menegaux, F.9
Gentilini, M.10
Mazier, D.11
-
91
-
-
0028269705
-
-
M. Tsuji, D. M. Mattei, R. S. Nussenzweig, D. Eichinger, F. Zavala, Parasitol, Res. 1994, 80, 16-21.
-
(1994)
Parasitol, Res.
, vol.80
, pp. 16-21
-
-
Tsuji, M.1
Mattei, D.M.2
Nussenzweig, R.S.3
Eichinger, D.4
Zavala, F.5
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