-
1
-
-
84942322948
-
Azo compounds
-
Dürr H, Bonas-Laurent H (eds). Elsevier: Amsterdam
-
Rau H. Azo compounds. In Studies in Organic Chemistry: Photochromism, Molecules and Systems, vol. 40, Dürr H, Bonas-Laurent H (eds). Elsevier: Amsterdam, 1990; 165-192.
-
(1990)
Studies in Organic Chemistry: Photochromism, Molecules and Systems
, vol.40
, pp. 165-192
-
-
Rau, H.1
-
2
-
-
33748241762
-
Control of the structure and functions of biomaterials by light
-
Willner I, Rubin S. Control of the structure and functions of biomaterials by light. Angew. Chem. Int. Ed. Engl. 1996; 35: 367-385.
-
(1996)
Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 367-385
-
-
Willner, I.1
Rubin, S.2
-
3
-
-
0642375842
-
Photoswitchable biomaterials - En route to optobioelectronic systems
-
Willner I. Photoswitchable biomaterials - en route to optobioelectronic systems. Acc. Chem. Res. 1997; 30: 347-356.
-
(1997)
Acc. Chem. Res.
, vol.30
, pp. 347-356
-
-
Willner, I.1
-
4
-
-
84990095651
-
A novel tris(azo)macrobicyclic molecule - Synthesis, photochemistry and isomer separation
-
Losensky H-W, Spelthann H, Ehlen A, Vögtle F, Bargon J. A novel tris(azo)macrobicyclic molecule - synthesis, photochemistry and isomer separation. Angew. Chem. Int. Ed. Engl. 1988; 27: 1189-1191.
-
(1988)
Angew. Chem. Int. Ed. Engl.
, vol.27
, pp. 1189-1191
-
-
Losensky, H.-W.1
Spelthann, H.2
Ehlen, A.3
Vögtle, F.4
Bargon, J.5
-
5
-
-
37049090729
-
Isomeric double-decker porphyrins bridged by four azobenzerie units
-
Neumann KH, Vögtle F. Isomeric double-decker porphyrins bridged by four azobenzerie units. J. Chem. Soc. Chem. Commun. 1988; 520-522.
-
(1988)
J. Chem. Soc. Chem. Commun.
, pp. 520-522
-
-
Neumann, K.H.1
Vögtle, F.2
-
6
-
-
0342627974
-
Synthesis and photoisomerization of an azobenzene derivative bearing two β-cyclodextrin units at both ends
-
Aoyagi T, Ueno A, Fukushima M, Osa T. Synthesis and photoisomerization of an azobenzene derivative bearing two β-cyclodextrin units at both ends. Macromol. Rapid Commun. 1998; 19: 103-105.
-
(1998)
Macromol. Rapid Commun.
, vol.19
, pp. 103-105
-
-
Aoyagi, T.1
Ueno, A.2
Fukushima, M.3
Osa, T.4
-
7
-
-
0031532002
-
Synthesis and characterization of photochromic dendrimers including a 1,3-alternate calix[4]arene as a core and azobenzene moieties as branches
-
Nagasaki T, Tamagaki S, Ogino K. Synthesis and characterization of photochromic dendrimers including a 1,3-alternate calix[4]arene as a core and azobenzene moieties as branches. Chem. Lett. 1997; 717-718.
-
(1997)
Chem. Lett.
, pp. 717-718
-
-
Nagasaki, T.1
Tamagaki, S.2
Ogino, K.3
-
9
-
-
0031591255
-
Photomodulation of conformational states of p-phenylazobenzyloxycarbonyl-L-proline and related peptides
-
Rudolph-Böhner S, Krüger M, Oesterhelt D, Moroder L, Nägele T, Wachtveitl J. Photomodulation of conformational states of p-phenylazobenzyloxycarbonyl-L-proline and related peptides. J. Photochem. Photobiol. A: Chem. 1997; 105: 235-248.
-
(1997)
J. Photochem. Photobiol. A: Chem.
, vol.105
, pp. 235-248
-
-
Rudolph-Böhner, S.1
Krüger, M.2
Oesterhelt, D.3
Moroder, L.4
Nägele, T.5
Wachtveitl, J.6
-
10
-
-
0020163940
-
Conformation and biological activity of cyclic-peptides
-
Kessler H. Conformation and biological activity of cyclic-peptides. Angew. Chem. Int. Ed. Engl. 1982; 21: 512-523.
-
(1982)
Angew. Chem. Int. Ed. Engl.
, vol.21
, pp. 512-523
-
-
Kessler, H.1
-
12
-
-
0007515648
-
Synthesis and optical properties of cyclic bis-cysteinyl-peptides and their linear precursors with a built-in light-switch
-
Tam JP, Kaumaya PTP (eds). Kluwer Academic Publ: Dordrecht
-
Schenk M, Rudolph-Böhner S, Wachtveitl J, Nägele T, Oesterhelt D, Moroder L. Synthesis and optical properties of cyclic bis-cysteinyl-peptides and their linear precursors with a built-in light-switch. In Peptides - Frontiers of Peptide Science, Tam JP, Kaumaya PTP (eds). Kluwer Academic Publ: Dordrecht, 1999; 313-314.
-
(1999)
Peptides - Frontiers of Peptide Science
, pp. 313-314
-
-
Schenk, M.1
Rudolph-Böhner, S.2
Wachtveitl, J.3
Nägele, T.4
Oesterhelt, D.5
Moroder, L.6
-
13
-
-
0027308079
-
Redox potentials of active site bis-cysteinyl fragments of thiol-protein oxidoreductases
-
Siedler F, Rudolph-Böhner S, Doi M, Musiol HJ, Moroder L. Redox potentials of active site bis-cysteinyl fragments of thiol-protein oxidoreductases. Biochemistry 1993; 32: 7488-7495.
-
(1993)
Biochemistry
, vol.32
, pp. 7488-7495
-
-
Siedler, F.1
Rudolph-Böhner, S.2
Doi, M.3
Musiol, H.J.4
Moroder, L.5
-
14
-
-
0029893791
-
Oxidative folding of cystine-rich peptides vs. regioselective cysteine pairing strategies
-
Moroder L, Besse D, Musiol HJ, Rudolph-Böhner S, Siedler F. Oxidative folding of cystine-rich peptides vs. regioselective cysteine pairing strategies. Biopolymers Peptide Sci. 1996; 40: 207-234.
-
(1996)
Biopolymers Peptide Sci.
, vol.40
, pp. 207-234
-
-
Moroder, L.1
Besse, D.2
Musiol, H.J.3
Rudolph-Böhner, S.4
Siedler, F.5
-
15
-
-
2442756314
-
Comparative analysis of the active site 3D-structures of thiol-protein oxidoreductases and related synthetic fragments
-
Maia, HLS (ed.). ESCOM: Leiden
-
Rudolph-Böhner S, Siedler F, Moroder L. Comparative analysis of the active site 3D-structures of thiol-protein oxidoreductases and related synthetic fragments. In Peptides 1994, Maia, HLS (ed.). ESCOM: Leiden, 1995; 578-579.
-
(1995)
Peptides 1994
, pp. 578-579
-
-
Rudolph-Böhner, S.1
Siedler, F.2
Moroder, L.3
-
16
-
-
0026422435
-
Convergent evolution of similar function in two structurally divergent enzymes
-
Kuriyan J, Krishna TSR, Wong L, Guenther B, Pahler A, Williams CH. Jr, Moldel P. Convergent evolution of similar function in two structurally divergent enzymes. Nature 1991; 352: 172-174.
-
(1991)
Nature
, vol.352
, pp. 172-174
-
-
Kuriyan, J.1
Krishna, T.S.R.2
Wong, L.3
Guenther, B.4
Pahler, A.5
Williams Jr., Ch.6
Moldel, P.7
-
17
-
-
37049155920
-
Bond lengths and resonance in the cis-azobenzene molecule
-
Hampson GC, Robertson JM. Bond lengths and resonance in the cis-azobenzene molecule. J. Chem. Soc. 1941; 409-413.
-
(1941)
J. Chem. Soc.
, pp. 409-413
-
-
Hampson, G.C.1
Robertson, J.M.2
-
18
-
-
2442750299
-
Photomodulation of conformational states in cyclic peptides by cis-trans isomerization of azobenzene
-
Fields GB, Tam JP, Barany G (eds). Kluwer Academic Press: Dordrecht, in press
-
Behrendt R, Renner C, Cramer J, Schenk M, Wachtveitl J, Oesterhelt D, Moroder L. Photomodulation of conformational states in cyclic peptides by cis-trans isomerization of azobenzene. In Peptides for the New Millennium, Fields GB, Tam JP, Barany G (eds). Kluwer Academic Press: Dordrecht, 2000 (in press).
-
(2000)
Peptides for the New Millennium
-
-
Behrendt, R.1
Renner, C.2
Cramer, J.3
Schenk, M.4
Wachtveitl, J.5
Oesterhelt, D.6
Moroder, L.7
-
19
-
-
0017495101
-
Rapid gas-chromatographic separation of amino acid enantiomers with a novel chiral stationary phase
-
Frank H, Nicholson GJ, Bayer E. Rapid gas-chromatographic separation of amino acid enantiomers with a novel chiral stationary phase. J. Chromatogr. Sci. 1977; 15: 174-176.
-
(1977)
J. Chromatogr. Sci.
, vol.15
, pp. 174-176
-
-
Frank, H.1
Nicholson, G.J.2
Bayer, E.3
-
20
-
-
85047670173
-
Cysteine racemization in peptide synthesis. A new and facile detection method
-
Siedler F, Weyher E, Moroder L. Cysteine racemization in peptide synthesis. A new and facile detection method. J. Peptide Sci. 1996; 2: 271-275.
-
(1996)
J. Peptide Sci.
, vol.2
, pp. 271-275
-
-
Siedler, F.1
Weyher, E.2
Moroder, L.3
-
21
-
-
0025671995
-
((9-Fluorenyl-methyl)oxy)carbonyl (FMOC) amino acid fluorides. Convenient new peptide coupling reagents applicable to the FMOC/tert-butyl strategy for solution and solid phase synthesis
-
Carpino LA, Sadat-Aalaee D, Chao HG, DeSelms RH. ((9-Fluorenyl-methyl)oxy)carbonyl (FMOC) amino acid fluorides. Convenient new peptide coupling reagents applicable to the FMOC/tert-butyl strategy for solution and solid phase synthesis. J. Am. Chem. Soc. 1990; 112: 9651-9652.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 9651-9652
-
-
Carpino, L.A.1
Sadat-Aalaee, D.2
Chao, H.G.3
DeSelms, R.H.4
-
22
-
-
26344475794
-
Methoden zur Herstellung und Umwandlung von Diarylazoverbindungen
-
Schündehütte KH. Methoden zur Herstellung und Umwandlung von Diarylazoverbindungen. HoubenWeyl, 4. Ed. 1965; 10/3: 215-465.
-
(1965)
HoubenWeyl, 4. Ed.
, vol.10
, Issue.3
, pp. 215-465
-
-
Schündehütte, K.H.1
-
23
-
-
0027963642
-
The synthesis of a light-switchable amino acid for inclusion into conformationally mobile peptides
-
Ulysse L, Chmielewski J. The synthesis of a light-switchable amino acid for inclusion into conformationally mobile peptides. Bioorg. Med. Chem. Lett. 1994; 4: 2145-2146.
-
(1994)
Bioorg. Med. Chem. Lett.
, vol.4
, pp. 2145-2146
-
-
Ulysse, L.1
Chmielewski, J.2
-
24
-
-
0014772602
-
Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides
-
Kaiser E, Colescott RC, Bossinger CD, Cook PI. Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides. Anal. Biochem. 1970; 34: 595-598.
-
(1970)
Anal. Biochem.
, vol.34
, pp. 595-598
-
-
Kaiser, E.1
Colescott, R.C.2
Bossinger, C.D.3
Cook, P.I.4
-
25
-
-
0000795175
-
A chloranil color test for monitoring coupling completeness in solid phase peptide synthesis
-
Gross E, Meienhofer J (eds). Pierce Chemical Co.: Rockford, IL
-
Christensen T. A chloranil color test for monitoring coupling completeness In solid phase peptide synthesis. In Peptides, Structure and Biological Functions, Gross E, Meienhofer J (eds). Pierce Chemical Co.: Rockford, IL, 1979; 385-388.
-
(1979)
Peptides, Structure and Biological Functions
, pp. 385-388
-
-
Christensen, T.1
-
26
-
-
0005215827
-
The 9-fluorenylmethyloxycarbonyl family of base-sensitive amino-protecting groups
-
Carpino LA. The 9-fluorenylmethyloxycarbonyl family of base-sensitive amino-protecting groups. Acc. Chem. Res. 1987; 20: 401-407.
-
(1987)
Acc. Chem. Res.
, vol.20
, pp. 401-407
-
-
Carpino, L.A.1
-
27
-
-
0028081131
-
A simple method for the protection of aryl amines as their t-butylcarbamoyl (Boc) derivatives
-
Kelly TA, McNeil DW. A simple method for the protection of aryl amines as their t-butylcarbamoyl (Boc) derivatives. Tetrahedron Lett. 1994; 48: 9003-9006.
-
(1994)
Tetrahedron Lett.
, vol.48
, pp. 9003-9006
-
-
Kelly, T.A.1
McNeil, D.W.2
-
28
-
-
0023655801
-
Improved synthesis and iodination of a cleavable photoactivated probe
-
Murphy HR, Harris HW Jr. Improved synthesis and iodination of a cleavable photoactivated probe. Anal. Biochem. 1987; 165: 88-95.
-
(1987)
Anal. Biochem.
, vol.165
, pp. 88-95
-
-
Murphy, H.R.1
Harris Jr., H.W.2
-
29
-
-
0031591253
-
Utrafast photoisomerization of azobenzene compounds
-
Wachtveitl J, Nägele T, Puell B, Zinth W, Krüger M, Rudolph-Böhner S, Oesterhelt D, Moroder L. Utrafast photoisomerization of azobenzene compounds. J. Photochem. Photobiol. A: Chem. 1997; 105: 283-288.
-
(1997)
J. Photochem. Photobiol. A: Chem.
, vol.105
, pp. 283-288
-
-
Wachtveitl, J.1
Nägele, T.2
Puell, B.3
Zinth, W.4
Krüger, M.5
Rudolph-Böhner, S.6
Oesterhelt, D.7
Moroder, L.8
-
30
-
-
0028004425
-
Redox-active bis-cysteinyl peptides. I. Synthesis of cyclic cystinyl peptides by conventional methods in solution and solid support
-
Musiol HJ, Siedler F, Quarzago D, Moroder L. Redox-active bis-cysteinyl peptides. I. Synthesis of cyclic cystinyl peptides by conventional methods in solution and solid support. Biopolymers 1994; 34: 1553-1562.
-
(1994)
Biopolymers
, vol.34
, pp. 1553-1562
-
-
Musiol, H.J.1
Siedler, F.2
Quarzago, D.3
Moroder, L.4
-
31
-
-
0025014627
-
PyBOP - A new peptide coupling reagent devoid of toxic byproducts
-
Coste J, Lenguyen D, Castro B. PyBOP - A new peptide coupling reagent devoid of toxic byproducts. Tetrahedron Lett. 1990; 31: 205-208.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 205-208
-
-
Coste, J.1
Lenguyen, D.2
Castro, B.3
-
32
-
-
0004621088
-
A comparative study on the synthesis of cysteinyl-peptides by conventional methods in solution and on solid supports
-
Hodges RS, Smith JA (eds). ESCOM: Leiden
-
Musiol HJ, Quarzago D, Scharf R, Moroder L. A comparative study on the synthesis of cysteinyl-peptides by conventional methods in solution and on solid supports. In Peptides: Chemistry, Structure and Biology, Hodges RS, Smith JA (eds). ESCOM: Leiden, 1994; 62-64.
-
(1994)
Peptides: Chemistry, Structure and Biology
, pp. 62-64
-
-
Musiol, H.J.1
Quarzago, D.2
Scharf, R.3
Moroder, L.4
-
33
-
-
0000277428
-
Occurence and minimization of cysteine racemization during stepwise solid-phase synthesis
-
Han YX, Albericio F, Barany G. Occurence and minimization of cysteine racemization during stepwise solid-phase synthesis. J. Org. Chem. 1997; 62: 4307-4312.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 4307-4312
-
-
Han, Y.X.1
Albericio, F.2
Barany, G.3
-
34
-
-
0024359592
-
Synthesis of protected peptide-fragments using substituted triphenylmethyl resins
-
Barlos K, Gatos D, Kallitsis J, Papaphotiu G, Sotiriu P, Yao WQ, Schäfer W. Synthesis of protected peptide-fragments using substituted triphenylmethyl resins. Tetrahedron Lett. 1989; 30: 3943-3946.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 3943-3946
-
-
Barlos, K.1
Gatos, D.2
Kallitsis, J.3
Papaphotiu, G.4
Sotiriu, P.5
Yao, W.Q.6
Schäfer, W.7
-
35
-
-
37049100132
-
A mild procedure for solid phase peptide synthesis: Use of fluorenylmethoxycarbonylamino-acids
-
Atherton E, Fox H, Harkiss D, Logan CJ, Sheppard RC, Williams BJ. A mild procedure for solid phase peptide synthesis: use of fluorenylmethoxycarbonylamino-acids. J. Chem. Soc. Commun. 1978; 537-539.
-
(1978)
J. Chem. Soc. Commun.
, pp. 537-539
-
-
Atherton, E.1
Fox, H.2
Harkiss, D.3
Logan, C.J.4
Sheppard, R.C.5
Williams, B.J.6
-
37
-
-
37049074206
-
A new reagent for the cleavage of fully protected peptides synthesised on 2-chlorotrityl chloride resin
-
Bollhagen R Schmiedberger M, Barlos K, Grell E. A new reagent for the cleavage of fully protected peptides synthesised on 2-chlorotrityl chloride resin. J. Chem. Soc. Chem. Commun. 1994; 2559-2560.
-
(1994)
J. Chem. Soc. Chem. Commun.
, pp. 2559-2560
-
-
Bollhagen, R.1
Schmiedberger, M.2
Barlos, K.3
Grell, E.4
-
38
-
-
0001153517
-
Selective reduction of disulfids by tris(2-carboxyethyl)phosphine
-
Burns JA, Butler JC, Moran J, Whitesides GM. Selective reduction of disulfids by tris(2-carboxyethyl)phosphine. J. Org. Chem. 1991; 56: 2648-2650.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 2648-2650
-
-
Burns, J.A.1
Butler, J.C.2
Moran, J.3
Whitesides, G.M.4
-
39
-
-
84936324313
-
Zur Synthese symmetrischer und unsymmetrischer Cystinpeptide
-
Hanson H, Jakubke HD (eds). North-Holland Publ. Co.: Amsterdam, London
-
Arold H, Eule M. Zur Synthese symmetrischer und unsymmetrischer Cystinpeptide. In Peptides 1972, Hanson H, Jakubke HD (eds). North-Holland Publ. Co.: Amsterdam, London, 1972; 78-89.
-
(1972)
Peptides 1972
, pp. 78-89
-
-
Arold, H.1
Eule, M.2
-
40
-
-
2442728118
-
Photomodulation of conformational states of cyclic peptides with a backbone-azobenzene moiety
-
Behrendt R, Renner C, Schenk M, Wang F, Wachtveitl J, Oesterhelt D, Moroder L. Photomodulation of conformational states of cyclic peptides with a backbone-azobenzene moiety. Angew. Chem. Int. Ed. Engl. 1999; 17.
-
(1999)
Angew. Chem. Int. Ed. Engl.
, pp. 17
-
-
Behrendt, R.1
Renner, C.2
Schenk, M.3
Wang, F.4
Wachtveitl, J.5
Oesterhelt, D.6
Moroder, L.7
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