-
1
-
-
0027626495
-
Noncoded residues as building blocks in the design of specific secondary structure: Symmetrically disubstituted glycine and alanine
-
Di Blasio B, Pavone V, Lombardi A, Pedone C, Benedetti E. Noncoded residues as building blocks in the design of specific secondary structure: Symmetrically disubstituted glycine and alanine. Biopolymers 1993; 33: 1037-1049.
-
(1993)
Biopolymers
, vol.33
, pp. 1037-1049
-
-
Di Blasio, B.1
Pavone, V.2
Lombardi, A.3
Pedone, C.4
Benedetti, E.5
-
2
-
-
0030057522
-
X-ray crystallography of peptides: The contributions of the Italian laboratories
-
Benedetti E. X-ray crystallography of peptides: The contributions of the Italian laboratories. Biopolymers 1996; 40: 3-44.
-
(1996)
Biopolymers
, vol.40
, pp. 3-44
-
-
Benedetti, E.1
-
5
-
-
0033983558
-
The crystal structure of Afc-containing peptides
-
Lombardi A, Simone GD, Galdiero S, Nastri F, Di Costanzo L, Makihira K, Yamada T, Pavone V. The crystal structure of Afc-containing peptides. Biopolymers 2000; 53: 150-160.
-
(2000)
Biopolymers
, vol.53
, pp. 150-160
-
-
Lombardi, A.1
Simone, G.D.2
Galdiero, S.3
Nastri, F.4
Di Costanzo, L.5
Makihira, K.6
Yamada, T.7
Pavone, V.8
-
6
-
-
0001324643
-
-
Ugi I (ed.). Academic Press: New York and London
-
Gokel G, Hoffmann P, Kleimann H, Klusacek H, Ludke G, Marquaerding D, Ugi I. In Isonitrile Chemistry, Ugi I (ed.). Academic Press: New York and London, 1971; 145-199.
-
(1971)
Isonitrile Chemistry
, pp. 145-199
-
-
Gokel, G.1
Hoffmann, P.2
Kleimann, H.3
Klusacek, H.4
Ludke, G.5
Marquaerding, D.6
Ugi, I.7
-
7
-
-
2542509173
-
Multicomponent reaction with isocyanides
-
Dömling A, Ugi I. Multicomponent reaction with isocyanides. Angew. Chem. Int. Ed. 2000; 39: 3168-3210.
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 3168-3210
-
-
Dömling, A.1
Ugi, I.2
-
8
-
-
0141905834
-
An improved approach for the synthesis of α,α-dialkyl glycine derivatives by the Ugi-Passerini reactions
-
Costa SPG, Maia HLS, Pereira-Lima SMMA. An improved approach for the synthesis of α,α-dialkyl glycine derivatives by the Ugi-Passerini reactions. Org. Biomol. Chem. 2003; 1: 1475-1479.
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 1475-1479
-
-
Costa, S.P.G.1
Maia, H.L.S.2
Pereira-Lima, S.M.M.A.3
-
9
-
-
0346369703
-
Synthesis of α,α-diisopropylglycine by the modified Ugi reaction at high pressure
-
Yamada T, Yanagi T, Omote Y, Miyazawa T, Kuwata S, Sugiura M, Matsumoto K. Synthesis of α,α-diisopropylglycine by the modified Ugi reaction at high pressure. Chem. Express 1991; 6: 575-578.
-
(1991)
Chem. Express
, vol.6
, pp. 575-578
-
-
Yamada, T.1
Yanagi, T.2
Omote, Y.3
Miyazawa, T.4
Kuwata, S.5
Sugiura, M.6
Matsumoto, K.7
-
10
-
-
84944200721
-
HPLC separation and conformation of peptide diastereomers containing α,α-dialkylglycine
-
Bayer J (ed.). Walter de Gruyter & Co.: Berlin, New York
-
Yamada T, Nakao M, Yanagi T, Miyazawa T, Kuwata S. HPLC separation and conformation of peptide diastereomers containing α,α-dialkylglycine. In Peptides 1988, Bayer J (ed.). Walter de Gruyter & Co.: Berlin, New York, 1989; 301-303.
-
(1989)
Peptides 1988
, pp. 301-303
-
-
Yamada, T.1
Nakao, M.2
Yanagi, T.3
Miyazawa, T.4
Kuwata, S.5
-
11
-
-
37049081057
-
Four-component condensation (Ugi reaction) at high pressure: Novel synthesis of peptides containing very bulky α,α-disubstituted glycines
-
Yamada T, Yanagi T, Omote Y, Miyazawa T, Kuwata S, Sugiura M, Matsumoto K. Four-component condensation (Ugi reaction) at high pressure: Novel synthesis of peptides containing very bulky α,α-disubstituted glycines. J. Chem. Soc. Chem. Commun. 1990; 1640-1641.
-
(1990)
J. Chem. Soc. Chem. Commun.
, pp. 1640-1641
-
-
Yamada, T.1
Yanagi, T.2
Omote, Y.3
Miyazawa, T.4
Kuwata, S.5
Sugiura, M.6
Matsumoto, K.7
-
12
-
-
0028627725
-
α,α-disubstituted tripeptides: X-ray crystal structures of Z-Aib-Dph-Gly-OMe and Bz-Dph-Dph-Gly-OMe
-
α,α-disubstituted tripeptides: X-ray crystal structures of Z-Aib-Dph-Gly-OMe and Bz-Dph-Dph-Gly-OMe. Biopolymers 1994; 34: 1595-1604.
-
(1994)
Biopolymers
, vol.34
, pp. 1595-1604
-
-
Pavone, V.1
Lombardi, A.2
Saviano, M.3
Di Blasio, B.4
Nastri, F.5
Fattorusso, R.6
Zaccaro, L.7
Maglio, O.8
Yamada, T.9
Omote, Y.10
Kuwata, S.11
-
13
-
-
0031989394
-
α,α-diphenylglycine: Folded vs extended structure in Døg-containing tripeptides
-
α,α-diphenylglycine: Folded vs extended structure in Døg-containing tripeptides. J. Pept. Sci. 1998; 4: 21-32.
-
(1998)
J. Pept. Sci.
, vol.4
, pp. 21-32
-
-
Pavone, V.1
Lombard, A.2
Saviano, M.3
Nastri, F.4
Zaccaro, L.5
Maglio, O.6
Pedone, C.7
Omote, Y.8
Yamanaka, Y.9
Yamada, T.10
-
14
-
-
0031852604
-
Synthesis of tripeptides containing α,α-diphenylglycine by the modified Ugi reaction
-
Yamada T, Omote Y, Yamanaka Y, Miyazawa T, Kuwata S. Synthesis of tripeptides containing α,α-diphenylglycine by the modified Ugi reaction. Synthesis 1998: 991-998.
-
(1998)
Synthesis
, pp. 991-998
-
-
Yamada, T.1
Omote, Y.2
Yamanaka, Y.3
Miyazawa, T.4
Kuwata, S.5
-
15
-
-
4644282927
-
A novel intramolecular hydrogen bonding between a side-chain pyridine ring and an amide hydrogen of the peptide backbone in tripeptides containing the new amino acid, α,α-di(2-pyridyl)glycine
-
Yamada T, Ichino T, Hanyu M, Ninomiya D, Yanagihara R, Miyazawa T, Murashima T. A novel intramolecular hydrogen bonding between a side-chain pyridine ring and an amide hydrogen of the peptide backbone in tripeptides containing the new amino acid, α,α-di(2-pyridyl)glycine. Org. Biomol. Chem. 2004; 2: 2335-2339
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 2335-2339
-
-
Yamada, T.1
Ichino, T.2
Hanyu, M.3
Ninomiya, D.4
Yanagihara, R.5
Miyazawa, T.6
Murashima, T.7
-
16
-
-
4644351252
-
Conformational and coordination properties of a peptide containing the novel α,α-bis(2-pyridyl)glycine amino acid
-
Di Costanzo L, Geremia S, Randaccio R, Ichino T, Yanagihara R, Yamada T, Marasco D, Lombardi A, Pavone V. Conformational and coordination properties of a peptide containing the novel α,α-bis(2-pyridyl)glycine amino acid. Dalton Trans. 2003; 787-792.
-
(2003)
Dalton Trans.
, pp. 787-792
-
-
Di Costanzo, L.1
Geremia, S.2
Randaccio, R.3
Ichino, T.4
Yanagihara, R.5
Yamada, T.6
Marasco, D.7
Lombardi, A.8
Pavone, V.9
-
17
-
-
33544456080
-
Conformations and metal-complex formation of tripeptides containing α,α-disubstituted glycine with pyridine rings
-
Shioiri T (ed.). Protein Research Foundation: Osaka
-
Yamada T, Ichino T, Yanagihara R, Miyazawa T. Conformations and metal-complex formation of tripeptides containing α,α-disubstituted glycine with pyridine rings. In Peptide Science 2000, Shioiri T (ed.). Protein Research Foundation: Osaka 2001; 77-80.
-
(2001)
Peptide Science 2000
, pp. 77-80
-
-
Yamada, T.1
Ichino, T.2
Yanagihara, R.3
Miyazawa, T.4
-
18
-
-
33749100952
-
Recent developments in solid-phase organic synthesis
-
Brown RCD. Recent developments in solid-phase organic synthesis. J. Chem. Soc., Perkin Trans. 1 1998; 3293-3320.
-
(1998)
J. Chem. Soc. Perkin Trans.
, vol.1
, pp. 3293-3320
-
-
Brown, R.C.D.1
-
19
-
-
33646449394
-
Carbon-carbon bond forming solid-phase reaction
-
Lorsbach BA, Kurth M. Carbon-carbon bond forming solid-phase reaction. Chem. Rev. 1999; 99: 1549-1581.
-
(1999)
Chem. Rev.
, vol.99
, pp. 1549-1581
-
-
Lorsbach, B.A.1
Kurth, M.2
-
20
-
-
0035128271
-
Carbon-carbon bond formang solid-phase reaction part 2
-
Sammelson RE, Kurth M. Carbon-carbon bond formang solid-phase reaction part 2. Chem. Rev. 2001; 101: 137-202.
-
(2001)
Chem. Rev.
, vol.101
, pp. 137-202
-
-
Sammelson, R.E.1
Kurth, M.2
-
21
-
-
0037191613
-
Synthesis of chiral chromium tricarbonyl labeled thymine PNA monomers via the Ugi reaction
-
Baldoil C, Maiorana S, Licandro E, Zinzalla G, Perdicchia D. Synthesis of chiral chromium tricarbonyl labeled thymine PNA monomers via the Ugi reaction. Org. Lett. 2002; 4: 4341-4344.
-
(2002)
Org. Lett.
, vol.4
, pp. 4341-4344
-
-
Baldoil, C.1
Maiorana, S.2
Licandro, E.3
Zinzalla, G.4
Perdicchia, D.5
-
22
-
-
0346970836
-
A versatile synthesis of α-amino acid derivatives via the Ugi four-component condensation with a novel convertible isonitrile
-
Rikimura K, Yanagisawa A, Kan T, Fukuyama T. A versatile synthesis of α-amino acid derivatives via the Ugi four-component condensation with a novel convertible isonitrile. Synlett. 2003; 41-44.
-
(2003)
Synlett.
, pp. 41-44
-
-
Rikimura, K.1
Yanagisawa, A.2
Kan, T.3
Fukuyama, T.4
-
23
-
-
0037938842
-
Solid-phase synthesis of five-dimensional libraries via a tandem Ptasis-Ugi multi-component condensation reaction
-
Portlock DE, Naskal D, West L, Ostaszewski R, Chen JJ. Solid-phase synthesis of five-dimensional libraries via a tandem Ptasis-Ugi multi-component condensation reaction. Tetrahedron Lett. 2003; 44: 5121-5124.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 5121-5124
-
-
Portlock, D.E.1
Naskal, D.2
West, L.3
Ostaszewski, R.4
Chen, J.J.5
-
24
-
-
0042158218
-
New method for the preparation of solid-phase bound isocyanocarboxyric acid and Ugi reaction therewith
-
Henkel B, Sax M, Dömling A. New method for the preparation of solid-phase bound isocyanocarboxyric acid and Ugi reaction therewith. Tetrahedron Lett. 2003; 44: 7015-7018.
-
(2003)
Tetrahedron Lett.
, vol.44
, pp. 7015-7018
-
-
Henkel, B.1
Sax, M.2
Dömling, A.3
-
25
-
-
7444243162
-
Synthesis of tripeptides containing a very crowded α,α-disubstituted glycine with pyridine rings by solid-phase Ugi reaction
-
Hanyu M, Murashima T, Miyazawa T, Yamada T. Synthesis of tripeptides containing a very crowded α,α-disubstituted glycine with pyridine rings by solid-phase Ugi reaction. Tetrahedron Lett. 2004; 45: 8871-8874.
-
(2004)
Tetrahedron Lett.
, vol.45
, pp. 8871-8874
-
-
Hanyu, M.1
Murashima, T.2
Miyazawa, T.3
Yamada, T.4
-
26
-
-
84981584650
-
Studies on polypeptides XXXII. Solid-phase synthesis of RNase S-peptide 1-14 analogues; replacement of histidine-12 by β-(2-pyridyl)-L-alanine and β-(4-pyridyl)-L-alanine
-
Hoes C, Raap J, Bloemhoff W, Kerling KET. Studies on polypeptides XXXII. Solid-phase synthesis of RNase S-peptide 1-14 analogues; replacement of histidine-12 by β-(2-pyridyl)-L-alanine and β-(4-pyridyl)-L-alanine. Recl. J. Royal Netherlands Chem. Soc. 1980; 99: 99-104.
-
(1980)
Recl. J. Royal Netherlands Chem. Soc.
, vol.99
, pp. 99-104
-
-
Hoes, C.1
Raap, J.2
Bloemhoff, W.3
Kerling, K.E.T.4
-
27
-
-
84981648976
-
Studies on polypeptides XXXIX. The role of the imidazole tele-nitrogen atom of histidine-12 in the catalytic action of RNase S'
-
Hoes C, Raap J, Kerling KET, Havinga E. Studies on polypeptides XXXIX. The role of the imidazole tele-nitrogen atom of histidine-12 in the catalytic action of RNase S'. Recl. Trav. Chim. Pays-Bas 1983; 102: 140-147.
-
(1983)
Recl. Trav. Chim. Pays-Bas.
, vol.102
, pp. 140-147
-
-
Hoes, C.1
Raap, J.2
Kerling, K.E.T.3
Havinga, E.4
-
29
-
-
0000419317
-
(S)-2a-amino-2,2′-bipyridine-6-propanoic acid: A versatile amino acid for de novo metalloprotein design
-
Imperiali B, Fisher SL. (S)-2a-amino-2,2′-bipyridine-6-propanoic acid: A versatile amino acid for de novo metalloprotein design. J. Am. Chem. Soc. 1991; 113: 8527-8528.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 8527-8528
-
-
Imperiali, B.1
Fisher, S.L.2
-
30
-
-
0011516931
-
Stereoselective synthesis and peptide incorporation of (S)-α-amino-(2,2′-bipyridine)-6-propanoic acid
-
Imperiali B, Fisher SL. Stereoselective synthesis and peptide incorporation of (S)-α-amino-(2,2′-bipyridine)-6-propanoic acid. J. Org. Chem. 1992; 57: 757-759.
-
(1992)
J. Org. Chem.
, vol.57
, pp. 757-759
-
-
Imperiali, B.1
Fisher, S.L.2
-
31
-
-
0000329492
-
Chemoenzymatic synthesis of 2-amino-3-(2,2′-bipyridinyl)propanic acids
-
Imperiali B, Prins TJ, Fisher S. Chemoenzymatic synthesis of 2-amino-3-(2,2′-bipyridinyl)propanic acids. J. Org. Chem. 1993; 58: 1613-1616.
-
(1993)
J. Org. Chem.
, vol.58
, pp. 1613-1616
-
-
Imperiali, B.1
Prins, T.J.2
Fisher, S.3
-
32
-
-
0028136765
-
Intercalator amino acids: Synthesis of heteroaryl alanines
-
Krippner GY, Harding MM. Intercalator amino acids: synthesis of heteroaryl alanines. Tetrahedron: Asymmetry 1994; 5: 1793-1804.
-
(1994)
Tetrahedron: Asymmetry
, vol.5
, pp. 1793-1804
-
-
Krippner, G.Y.1
Harding, M.M.2
-
33
-
-
0028814357
-
Synthesis of redox derivatives of lysine and their use in solid-phase synthesis of a light-harvesting peptide
-
McCafferty DG, Bishop BM, Wall CG, Hughes SG, Mecklenberg SL, Meyer TJ, Erickson BW. Synthesis of redox derivatives of lysine and their use in solid-phase synthesis of a light-harvesting peptide. Tetrahedron 1995; 51: 1093-1106.
-
(1995)
Tetrahedron
, vol.51
, pp. 1093-1106
-
-
McCafferty, D.G.1
Bishop, B.M.2
Wall, C.G.3
Hughes, S.G.4
Mecklenberg, S.L.5
Meyer, T.J.6
Erickson, B.W.7
-
34
-
-
0030469797
-
New synthetic amino acid for the design and synthesis of peptide-based metal ion sensors
-
Torrado A, Imperiali B. New synthetic amino acid for the design and synthesis of peptide-based metal ion sensors. J. Org. Chem. 1996; 61: 8940-8948.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 8940-8948
-
-
Torrado, A.1
Imperiali, B.2
-
35
-
-
1542615631
-
Molecular design of functional peptides by utilizing unnatural amino acid: Toward artificial and photofunctional protein
-
Ishida H, Kyakuno M, Oishi S. Molecular design of functional peptides by utilizing unnatural amino acid: Toward artificial and photofunctional protein. Biopolymers (Pept. Sci.) 2004; 76: 69-82.
-
(2004)
Biopolymers (Pept. Sci.)
, vol.76
, pp. 69-82
-
-
Ishida, H.1
Kyakuno, M.2
Oishi, S.3
-
36
-
-
0042372396
-
Synthesis of (5-hydroxy-2-pyridyl)glycine. Oxazole formation in the Bucherer-Bergs reaction. Studies on amino acid VI
-
Herdeis C, Gebhard R. Synthesis of (5-hydroxy-2-pyridyl)glycine. Oxazole formation in the Bucherer-Bergs reaction. Studies on amino acid VI. Heterocycles 1986; 24: 1019-1024.
-
(1986)
Heterocycles
, vol.24
, pp. 1019-1024
-
-
Herdeis, C.1
Gebhard, R.2
-
37
-
-
0023351850
-
Aminosäuren. 8. Mitt. Peptidsynthesen mit (±)5-Hydroxy-2-pyridylglycin ((±)Pyg(5-OH)), einer neuen heterocyclisch suhstituierten Aminosäure
-
Herdeis C, Gebhard R. Aminosäuren. 8. Mitt. Peptidsynthesen mit (±)5-Hydroxy-2-pyridylglycin ((±)Pyg(5-OH)), einer neuen heterocyclisch suhstituierten Aminosäure. Arch. Pharm. (Weinheim) 1987; 320: 546-553.
-
(1987)
Arch. Pharm. (Weinheim)
, vol.320
, pp. 546-553
-
-
Herdeis, C.1
Gebhard, R.2
-
38
-
-
33544454759
-
Synthesis and conformational study of tripeptides containing the amino acid with a pyridine ring
-
Aoyagi H (ed.). Protein Research Foundation: Osaka
-
Yamada T, Ninomiya D, Hara A, Yanagihara R, Miyazawa T. Synthesis and conformational study of tripeptides containing the amino acid with a pyridine ring. In Peptide Science 2001, Aoyagi H (ed.). Protein Research Foundation: Osaka, 2002; 277-280.
-
(2002)
Peptide Science 2001
, pp. 277-280
-
-
Yamada, T.1
Ninomiya, D.2
Hara, A.3
Yanagihara, R.4
Miyazawa, T.5
-
39
-
-
0032493480
-
Solution and solid-phase combinatorial synthesis of peptidomimetic library containing diversified α-methylated amino acid
-
Kim AW, Shin YS, Ro S. Solution and solid-phase combinatorial synthesis of peptidomimetic library containing diversified α-methylated amino acid. Bioorg. Med Chem. Lett. 1998; 8: 1665-1668.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 1665-1668
-
-
Kim, A.W.1
Shin, Y.S.2
Ro, S.3
-
41
-
-
0033592053
-
Hydrogen bonded antiparallel β-strand motifs promoted by 2,6-bis(carbamoylpeptide)pyridine
-
Yu Q, Baroni TE, Liable-Sands L, Yap GPA, Rheingold AL, Borovik AS. Hydrogen bonded antiparallel β-strand motifs promoted by 2,6-bis(carbamoylpeptide)pyridine. Chem. Commun. 1999; 1467-1468.
-
(1999)
Chem. Commun.
, pp. 1467-1468
-
-
Yu, Q.1
Baroni, T.E.2
Liable-Sands, L.3
Yap, G.P.A.4
Rheingold, A.L.5
Borovik, A.S.6
|