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Volumn 9, Issue 8, 2003, Pages 471-501

The cyclization of peptides and depsipeptides

Author keywords

Cyclic depsipeptides; Cyclodepsipeptides; Cyclopeptides; Head to tail cyclization; Heterodetic cyclic peptides; Homodetic cyclic peptides; Macrocyclization of peptides; Macrolactamization; Peptide cyclization; Side chain to side chain cyclization

Indexed keywords

AMIDE; ANTAMANIDE; CYCLO(DEXTRO TRYPTOPHYL DEXTRO ASPARTYLPROLYL DEXTRO VALYLLEUCYL); CYCLOPEPTIDE; CYCLOSPORIN A; CYCLOSPORIN DERIVATIVE; CYCLOSPORIN O; DECAPEPTIDE; DEPSIPEPTIDE; DIDEMNIN B; ENNIATIN; EPTIFIBATIDE; GONADORELIN ANTAGONIST; GRAMICIDIN S; HEPTAPEPTIDE; HEXAPEPTIDE; MACROCYCLIC COMPOUND; NONAPEPTIDE; OCTAPEPTIDE; OCTREOTIDE; PENTAPEPTIDE; PHOSPHONIUM DERIVATIVE; PIPERAZINE DERIVATIVE; PROTEIN PRECURSOR; RESIN; TETRAPEPTIDE; TRIPEPTIDE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; VALINOMYCIN;

EID: 0041475925     PISSN: 10752617     EISSN: None     Source Type: Journal    
DOI: 10.1002/psc.491     Document Type: Review
Times cited : (407)

References (219)
  • 1
    • 0000698830 scopus 로고    scopus 로고
    • Synthesis of cyclic disulfide peptides: Comparison of oxidation methods
    • Eichler J, Houghten RA. Synthesis of cyclic disulfide peptides: comparison of oxidation methods. Protein Pept. Lett. 1997; 4: 157-164.
    • (1997) Protein Pept. Lett. , vol.4 , pp. 157-164
    • Eichler, J.1    Houghten, R.A.2
  • 2
    • 0030670496 scopus 로고    scopus 로고
    • Disulfide bond formation in peptides
    • Hargittai B, Barany G. Disulfide bond formation in peptides. Methods Enzymol. 1997; 289: 198-221.
    • (1997) Methods Enzymol. , vol.289 , pp. 198-221
    • Hargittai, B.1    Barany, G.2
  • 3
    • 0042790440 scopus 로고
    • 34, Chapters Specialist Periodical Reports, Royal Society of Chemistry, eds. Young GT (Vol 1-4), Sheppard RC (5-13). Jones JH (14-23), Davies JS (24-32), Davies JS and Barrett GC (33-34)
    • Chapters in 'Amino Acids, Peptides and Proteins', Specialist Periodical Reports, Royal Society of Chemistry, Volumes 1-34 (1969-2003) eds. Young GT (Vol 1-4), Sheppard RC (5-13). Jones JH (14-23), Davies JS (24-32), Davies JS and Barrett GC (33-34).
    • (1969) 'Amino Acids, Peptides and Proteins' , vol.1
  • 4
    • 0000915203 scopus 로고
    • Bioactive sponge peptides
    • Fusetani N, Matsunaga S. Bioactive sponge peptides. Chem. Rev. 1993; 93: 1793-1806.
    • (1993) Chem. Rev. , vol.93 , pp. 1793-1806
    • Fusetani, N.1    Matsunaga, S.2
  • 6
    • 0000314051 scopus 로고
    • Synthetic studies of biologically active marine cyclopeptides
    • Wipf P. Synthetic studies of biologically active marine cyclopeptides. Chem. Rev. 1995; 95: 2115-2134.
    • (1995) Chem. Rev. , vol.95 , pp. 2115-2134
    • Wipf, P.1
  • 7
    • 0034142130 scopus 로고    scopus 로고
    • Highlights of marine natural products chemistry (1972-1999)
    • Faulkner DJ. Highlights of marine natural products chemistry (1972-1999). Nat. Pro. Rep. 2000; 17: 1-6.
    • (2000) Nat. Pro. Rep. , vol.17 , pp. 1-6
    • Faulkner, D.J.1
  • 10
    • 0021912607 scopus 로고
    • Synthesis of cyclosporine and analogues - Structural requirements for immunosuppressive activity
    • Wenger RM. Synthesis of cyclosporine and analogues - structural requirements for immunosuppressive activity. Angew. Chem. Int. Ed. 1985; 24: 77-85.
    • (1985) Angew. Chem. Int. Ed. , vol.24 , pp. 77-85
    • Wenger, R.M.1
  • 11
    • 0035995964 scopus 로고    scopus 로고
    • High yield synthesis of tentoxin, a cyclic tetrapeptide
    • Loiseau N, Cavalier F, Noel JP, Gomis JM. High yield synthesis of tentoxin, a cyclic tetrapeptide. J. Pept. Sci. 2002; 8: 335-346.
    • (2002) J. Pept. Sci. , vol.8 , pp. 335-346
    • Loiseau, N.1    Cavalier, F.2    Noel, J.P.3    Gomis, J.M.4
  • 13
    • 0019920627 scopus 로고
    • Structure of vancomycin - Evidence for an asparagine residue in the peptide
    • Harris CM, Harris TM. Structure of vancomycin -evidence for an asparagine residue in the peptide. J. Am. Chem. Soc. 1982; 104: 4293-4295.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 4293-4295
    • Harris, C.M.1    Harris, T.M.2
  • 14
    • 0033851437 scopus 로고    scopus 로고
    • Post-translationally modified bacteriocins - The lantibiotics
    • Guder A, Wiedemann I, Sahl HG. Post-translationally modified bacteriocins - the lantibiotics. Biopolymers 2000; 55: 62-73.
    • (2000) Biopolymers , vol.55 , pp. 62-73
    • Guder, A.1    Wiedemann, I.2    Sahl, H.G.3
  • 18
    • 0035686407 scopus 로고    scopus 로고
    • New reagents, reactions and peptidomimetics for drug design
    • Goodman M, Zapf C, Rew Y. New reagents, reactions and peptidomimetics for drug design Biopolymers 2001; 60: 229-245.
    • (2001) Biopolymers , vol.60 , pp. 229-245
    • Goodman, M.1    Zapf, C.2    Rew, Y.3
  • 19
    • 0036158878 scopus 로고    scopus 로고
    • Peptides as drugs: Is there a market?
    • Loffet A. Peptides as drugs: Is there a market? J. Pept. Sci. 2002; 8: 1-7.
    • (2002) J. Pept. Sci. , vol.8 , pp. 1-7
    • Loffet, A.1
  • 20
    • 0036636061 scopus 로고    scopus 로고
    • Peptides for the pharmaceutical market: Chemical synthesis and downstream processing on an industrial scale
    • Cappelletti S, Annoni P, DiGregorio G, Storace O, Pinori M. Peptides for the pharmaceutical market: Chemical synthesis and downstream processing on an industrial scale. Chim. Oggi/Chem. Today 2002; 20: 47-50.
    • (2002) Chim. Oggi/Chem. Today , vol.20 , pp. 47-50
    • Cappelletti, S.1    Annoni, P.2    DiGregorio, G.3    Storace, O.4    Pinori, M.5
  • 21
    • 0036635309 scopus 로고    scopus 로고
    • Large scale manufacturing methods for peptides - A status report
    • Verlander M. Large scale manufacturing methods for peptides - A status report. Chim. Oggi/Chem. Today 2002; 20: 62-66.
    • (2002) Chim. Oggi/Chem. Today , vol.20 , pp. 62-66
    • Verlander, M.1
  • 22
    • 0036636068 scopus 로고    scopus 로고
    • Trends in peptide chemistry 3. Natural cyclic peptides: Is the chemical synthesis commercially feasible?
    • Mizhiritskii M, Shpernat Y. Trends in peptide chemistry 3. Natural cyclic peptides: Is the chemical synthesis commercially feasible? Chim. Oggi/Chem. Today 2002; 20: 43-45.
    • (2002) Chim. Oggi/Chem. Today , vol.20 , pp. 43-45
    • Mizhiritskii, M.1    Shpernat, Y.2
  • 24
    • 0007193238 scopus 로고    scopus 로고
    • Chemical synthesis of natural product peptides: Coupling methods for the incorporation of non-coded amino acids into peptides
    • Humphrey JM, Chamberlin AR. Chemical synthesis of natural product peptides: Coupling methods for the incorporation of non-coded amino acids into peptides. Chem. Rev. 1997; 97: 2243-2266.
    • (1997) Chem. Rev. , vol.97 , pp. 2243-2266
    • Humphrey, J.M.1    Chamberlin, A.R.2
  • 26
    • 0036589386 scopus 로고    scopus 로고
    • Exploring privileged structures: The combinatorial synthesis of cyclic peptides
    • Horton DA, Bourne GT, Smythe ML. Exploring privileged structures: the combinatorial synthesis of cyclic peptides. J. Computer-Aided Mol. Design 2002; 16: 415-430.
    • (2002) J. Computer-Aided Mol. Design , vol.16 , pp. 415-430
    • Horton, D.A.1    Bourne, G.T.2    Smythe, M.L.3
  • 28
    • 0037261988 scopus 로고    scopus 로고
    • A revised guide to abbreviations in peptide science and a plea for conformity
    • Jones JH. A revised guide to abbreviations in peptide science and a plea for conformity. J. Pept. Sci. 2003; 9: 1-8.
    • (2003) J. Pept. Sci. , vol.9 , pp. 1-8
    • Jones, J.H.1
  • 30
    • 0041287686 scopus 로고
    • Gross E, Meienhoffer J (eds). Academic Press: Oxford
    • The Peptides: Analysis, Synthesis, Biology. Vol. 1. Gross E, Meienhoffer J (eds). Academic Press: Oxford, 1979; 433.
    • (1979) The Peptides: Analysis, Synthesis, Biology , vol.1 , pp. 433
  • 31
    • 0014704672 scopus 로고
    • Eine neue methode zur synthese von peptiden. Aktivierung der carboxylgruppe mit dicyclohexylcarbodiimide unter zuzatz von 1-Hydroxybenztriazole
    • Koenig W, Geiger R. Eine neue methode zur synthese von peptiden. Aktivierung der carboxylgruppe mit dicyclohexylcarbodiimide unter zuzatz von 1-Hydroxybenztriazole. Chem. Ber. 1970; 103: 788-798.
    • (1970) Chem. Ber. , vol.103 , pp. 788-798
    • Koenig, W.1    Geiger, R.2
  • 32
    • 0000726496 scopus 로고
    • The carbodiimide method
    • Gross E, Meienhoffer J (eds). Academic Press: New York
    • Rich DH, Singh J. The carbodiimide method. In The Peptides: Analysis, Synthesis, Biology, Gross E, Meienhoffer J (eds). Academic Press: New York, 1979; 1: 241-262.
    • (1979) The Peptides: Analysis, Synthesis, Biology , vol.1 , pp. 241-262
    • Rich, D.H.1    Singh, J.2
  • 33
    • 12044258245 scopus 로고
    • 1-Hydroxy-7-azabenzotriazole: An efficient peptide coupling additive
    • Carpino LA. 1-Hydroxy-7-azabenzotriazole: an efficient peptide coupling additive. J. Am. Chem. Soc. 1993; 115: 4397-4398.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 4397-4398
    • Carpino, L.A.1
  • 35
    • 0032770026 scopus 로고    scopus 로고
    • Effect of the amounts of additives on peptide coupling mediated by a water-soluble carbodiimide in alcohol
    • Nozaki S. Effect of the amounts of additives on peptide coupling mediated by a water-soluble carbodiimide in alcohol. J. Pept. Res. 1999; 54: 162-167.
    • (1999) J. Pept. Res. , vol.54 , pp. 162-167
    • Nozaki, S.1
  • 36
    • 0000419438 scopus 로고    scopus 로고
    • Synthesis and applications of cyclopeptides and depsipeptides
    • Davies JS, Howe J, Jayatilake J, Riley T. Synthesis and applications of cyclopeptides and depsipeptides. Lett. Pept. Sci. 1997; 4: 441-445.
    • (1997) Lett. Pept. Sci. , vol.4 , pp. 441-445
    • Davies, J.S.1    Howe, J.2    Jayatilake, J.3    Riley, T.4
  • 37
    • 0015520853 scopus 로고
    • Diphenylphosphoryl azide: A new convenient reagent for a modified Curtius reaction and for peptide synthesis
    • Shioiri T, Ninomiya K, Yamada S. Diphenylphosphoryl azide: A new convenient reagent for a modified Curtius reaction and for peptide synthesis. 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
  • 39
    • 0002006449 scopus 로고    scopus 로고
    • Solid phase synthesis of tailed cyclic peptides: The use of α-allyl-protected aspartic acid leads to an aspartimide and tetramethylguanidinium formation
    • Delforge D, Dieu M, Delaive E, Art M, Gillon B, Deuveese B, Raes M, van Beeumen J, Remacle J. Solid phase synthesis of tailed cyclic peptides: the use of α-allyl-protected aspartic acid leads to an aspartimide and tetramethylguanidinium formation. Lett. Pept. Sci. 1996; 3: 89-97.
    • (1996) Lett. Pept. Sci. , vol.3 , pp. 89-97
    • Delforge, D.1    Dieu, M.2    Delaive, E.3    Art, M.4    Gillon, B.5    Deuveese, B.6    Raes, M.7    van Beeumen, J.8    Remacle, J.9
  • 41
    • 0030715632 scopus 로고    scopus 로고
    • Spirocyclic peptidomimetics featuring 2,3- methano amino acids
    • Lim D, Burgess K. Spirocyclic peptidomimetics featuring 2,3- methano amino acids. J. Am. Chem Soc. 1997; 119: 9632-9640.
    • (1997) J. Am. Chem Soc. , vol.119 , pp. 9632-9640
    • Lim, D.1    Burgess, K.2
  • 44
    • 0000081593 scopus 로고
    • Solid phase synthesis of protected peptides on a polymer-bound oxime
    • DeGrado WF, Kaiser ET. Solid phase synthesis of protected peptides on a polymer-bound oxime. J. Org. Chem. 1982; 47: 3258-3261.
    • (1982) J. Org. Chem. , vol.47 , pp. 3258-3261
    • DeGrado, W.F.1    Kaiser, E.T.2
  • 45
    • 0035855309 scopus 로고    scopus 로고
    • Solid phase synthesis of cyclic peptides by oxidative cyclative cleavage of an aryl hydrazide linker - Synthesis of stylostatin 1
    • Rosenbaum C, Waldmann H. Solid phase synthesis of cyclic peptides by oxidative cyclative cleavage of an aryl hydrazide linker - Synthesis of stylostatin 1. Tetrahedron Lett. 2001; 42: 5677-5680.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 5677-5680
    • Rosenbaum, C.1    Waldmann, H.2
  • 46
    • 0028108821 scopus 로고
    • Peptide cyclisation on solid support: A fast and efficient route to small cyclopeptides
    • Richter LS, Tom JYK, Brunier JP. Peptide cyclisation on solid support: A fast and efficient route to small cyclopeptides. Tetrahedron Lett. 1995; 35: 5547-5550.
    • (1995) Tetrahedron Lett. , vol.35 , pp. 5547-5550
    • Richter, L.S.1    Tom, J.Y.K.2    Brunier, J.P.3
  • 47
    • 0033584984 scopus 로고    scopus 로고
    • Solid phase synthesis of head to tail cyclic peptides using a sulfonamide safety catch linker: The cleavage by cyclisation approach
    • Yang L, Morriello G. Solid phase synthesis of head to tail cyclic peptides using a sulfonamide safety catch linker: the cleavage by cyclisation approach. Tetrahedron Lett. 1999; 40: 8197-8200.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 8197-8200
    • Yang, L.1    Morriello, G.2
  • 49
    • 0027942225 scopus 로고
    • Solid phase synthesis of head to tail cyclic peptides via lysine side-chain
    • Alsina J, Rabonal F, Albericio F, Barany G. Solid phase synthesis of head to tail cyclic peptides via lysine side-chain. Tetrahedron Lett. 1994; 35: 9633-9636.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 9633-9636
    • Alsina, J.1    Rabonal, F.2    Albericio, F.3    Barany, G.4
  • 50
    • 0030061507 scopus 로고    scopus 로고
    • An approach to cyclic peptide libraries: Reducing epimerisation in medium-sized rings during solid phase synthesis
    • Spatola AF, Dorlak K, Romanovskis P. An approach to cyclic peptide libraries: reducing epimerisation in medium-sized rings during solid phase synthesis. Tetrahedron Lett. 1996; 37: 591-594.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 591-594
    • Spatola, A.F.1    Dorlak, K.2    Romanovskis, P.3
  • 51
    • 0032429560 scopus 로고    scopus 로고
    • Preparation of head to tail cyclic peptides via side chain attachment
    • Romanovskis P, Spatola AF. Preparation of head to tail cyclic peptides via side chain attachment. J. Pept. Res. 1998; 52: 356-374.
    • (1998) J. Pept. Res. , vol.52 , pp. 356-374
    • Romanovskis, P.1    Spatola, A.F.2
  • 52
    • 0034580303 scopus 로고    scopus 로고
    • Synthesis of a cyclic peptide library based on the somatostatin sequence using backbone amide linker approach
    • Bourne GT, Golding SW, Meutermans WDF, Smythe ML. Synthesis of a cyclic peptide library based on the somatostatin sequence using backbone amide linker approach. Lett. Pept. Sci. 2001; 7: 311-316.
    • (2001) Lett. Pept. Sci. , vol.7 , pp. 311-316
    • Bourne, G.T.1    Golding, S.W.2    Meutermans, W.D.F.3    Smythe, M.L.4
  • 53
    • 0032823018 scopus 로고    scopus 로고
    • Solid phase synthesis with tris (alkoxy) benzyl backbone amide cleavage
    • Alsina J, Jensen KJ, Albericio F, Barany G. Solid phase synthesis with tris (alkoxy) benzyl backbone amide cleavage. Chem-Eur. J. 1999; 5: 2787-2795.
    • (1999) Chem-Eur. J. , vol.5 , pp. 2787-2795
    • Alsina, J.1    Jensen, K.J.2    Albericio, F.3    Barany, G.4
  • 54
    • 0032134260 scopus 로고    scopus 로고
    • Solid phase synthesis of cyclic peptides; model studies involving i - (i+4) side chain-side chain cyclisation
    • Cavallaro V, Thompson P, Hearn M. Solid phase synthesis of cyclic peptides; model studies involving i - (i+4) side chain-side chain cyclisation. J. Pept. Sci. 1998; 4: 335-343.
    • (1998) J. Pept. Sci. , vol.4 , pp. 335-343
    • Cavallaro, V.1    Thompson, P.2    Hearn, M.3
  • 55
    • 0035078547 scopus 로고    scopus 로고
    • Preparation of side-chain to side-chain cyclic peptides by allyl and alloc strategy: Potential for library synthesis
    • Grieco P, Gitu PM, Hruby VJ. Preparation of side-chain to side-chain cyclic peptides by allyl and alloc strategy: potential for library synthesis. J. Pept. Sci. 2001; 57: 250-256.
    • (2001) J. Pept. Sci. , vol.57 , pp. 250-256
    • Grieco, P.1    Gitu, P.M.2    Hruby, V.J.3
  • 56
    • 0034888722 scopus 로고    scopus 로고
    • Facile synthesis of orthogonally protected amino acid building blocks for combinatorial N-backbone cyclic peptide chemistry
    • Gellerman G, Elgavi A, Salitra Y, Kramer M. Facile synthesis of orthogonally protected amino acid building blocks for combinatorial N-backbone cyclic peptide chemistry. J. Pept. Res. 2001; 57: 277-291.
    • (2001) J. Pept. Res. , vol.57 , pp. 277-291
    • Gellerman, G.1    Elgavi, A.2    Salitra, Y.3    Kramer, M.4
  • 57
    • 0030808964 scopus 로고    scopus 로고
    • Synthesis of large cyclic cystineknot peptide by orthogonal coupling strategy using unprotected peptide precursor
    • Tam JP, Lu YA. Synthesis of large cyclic cystineknot peptide by orthogonal coupling strategy using unprotected peptide precursor. Tetrahedron Lett. 1997; 38: 5599-5602.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5599-5602
    • Tam, J.P.1    Lu, Y.A.2
  • 58
    • 0033549108 scopus 로고    scopus 로고
    • Thia-Zip reaction for synthesis of large cyclic peptides: Mechanisms and applications
    • Tam JP, Lu YA, Yu Q. Thia-Zip reaction for synthesis of large cyclic peptides: mechanisms and applications. J. Am Chem. Soc. 1999; 121: 4316-4324.
    • (1999) J. Am Chem. Soc. , vol.121 , pp. 4316-4324
    • Tam, J.P.1    Lu, Y.A.2    Yu, Q.3
  • 59
    • 0033553118 scopus 로고    scopus 로고
    • Lactone and lactam library synthesis by silver ion assisted orthogonal cyclisation of unprotected peptides
    • Zhang L, Tam JP. Lactone and lactam library synthesis by silver ion assisted orthogonal cyclisation of unprotected peptides. J. Am Chem. Soc. 1999; 121: 3311-3320.
    • (1999) J. Am Chem. Soc. , vol.121 , pp. 3311-3320
    • Zhang, L.1    Tam, J.P.2
  • 60
    • 0032482508 scopus 로고    scopus 로고
    • A novel method to synthesise cyclic peptides
    • Shao Y, Lu W, Kent SBH. A novel method to synthesise cyclic peptides. Tetrahedron Lett. 1998; 39: 3911-3914.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 3911-3914
    • Shao, Y.1    Lu, W.2    Kent, S.B.H.3
  • 62
    • 0035383407 scopus 로고    scopus 로고
    • Enzymes for peptide cyclisation
    • Bordusa F. Enzymes for peptide cyclisation. Chem-Biochem 2001; 2: 405-409.
    • (2001) Chem.-Biochem. , vol.2 , pp. 405-409
    • Bordusa, F.1
  • 63
    • 0034648798 scopus 로고    scopus 로고
    • Peptide cyclisation catalysed by thioesterase domain of tyrocidine synthetase
    • Trauger JW, Kohli RM, Mootz HD, Marahiel MA, Walsh CT. Peptide cyclisation catalysed by thioesterase domain of tyrocidine synthetase. Nature 2000; 407: 215-218.
    • (2000) Nature , vol.407 , pp. 215-218
    • Trauger, J.W.1    Kohli, R.M.2    Mootz, H.D.3    Marahiel, M.A.4    Walsh, C.T.5
  • 64
    • 0037423499 scopus 로고    scopus 로고
    • Enzymology of acyl chain macrocyclisation in natural product biosynthesis
    • Kohli RM, Walsh CT. Enzymology of acyl chain macrocyclisation in natural product biosynthesis. Chem. Comm. (Cambridge) 2003; 297-307.
    • (2003) Chem. Comm. (Cambridge) , pp. 297-307
    • Kohli, R.M.1    Walsh, C.T.2
  • 65
    • 0028829779 scopus 로고
    • Enzymatic cyclisation of linear peptide esters using subtiligase
    • Jackson DY, Burnier JP, Wells JA. Enzymatic cyclisation of linear peptide esters using subtiligase. J. Am. Chem. Soc. 1995; 117: 819-820.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 819-820
    • Jackson, D.Y.1    Burnier, J.P.2    Wells, J.A.3
  • 68
    • 0031894588 scopus 로고    scopus 로고
    • Chemical ligation of unprotected peptides directly from a solid support
    • Camarero JA, Cotton GJ, Adeva A, Muir TW. Chemical ligation of unprotected peptides directly from a solid support. J. Pept. Res. 1998; 51: 303-316.
    • (1998) J. Pept. Res. , vol.51 , pp. 303-316
    • Camarero, J.A.1    Cotton, G.J.2    Adeva, A.3    Muir, T.W.4
  • 69
    • 0028300132 scopus 로고
    • Diketopiperazine cyclisation of Glu-Asp dipeptide esters and Asp racemisation during segment condensation
    • Fischer PM, Solbakken M, Undheim K. Diketopiperazine cyclisation of Glu-Asp dipeptide esters and Asp racemisation during segment condensation. Tetrahedron 1994; 50: 2277-2288.
    • (1994) Tetrahedron , vol.50 , pp. 2277-2288
    • Fischer, P.M.1    Solbakken, M.2    Undheim, K.3
  • 70
    • 0028077859 scopus 로고
    • Spontaneous diketopiperazine formation via end to end cyclisation of non-activated linear tripeptide. An unusual chemical reaction
    • Carpenter KA, Weltrowska G, Wilkes BC, Schmidt R, Schiller PW. Spontaneous diketopiperazine formation via end to end cyclisation of non-activated linear tripeptide. An unusual chemical reaction. J. Am. Chem. Soc. 1994; 116: 8450-8458.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 8450-8458
    • Carpenter, K.A.1    Weltrowska, G.2    Wilkes, B.C.3    Schmidt, R.4    Schiller, P.W.5
  • 71
    • 0030012632 scopus 로고    scopus 로고
    • t solid phase peptide synthesis using alkoxybenzyl ester anchoring linkages
    • t solid phase peptide synthesis using alkoxybenzyl ester anchoring linkages. Tetrahedron Lett. 1996; 37: 4195-4198.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 4195-4198
    • Alsina, J.1    Giralt, E.2    Albericio, F.3
  • 72
    • 0001689141 scopus 로고
    • Direct cleavage of peptides from a solid support into aqueous buffer. Application in simultaneous multiple peptide synthesis
    • Bray AM, Maeji NJ, Valerio RM, Campbell RA, Geysen HM. Direct cleavage of peptides from a solid support into aqueous buffer. Application in simultaneous multiple peptide synthesis. J. Org. Chem. 1991; 56: 6659-6666.
    • (1991) J. Org. Chem. , vol.56 , pp. 6659-6666
    • Bray, A.M.1    Maeji, N.J.2    Valerio, R.M.3    Campbell, R.A.4    Geysen, H.M.5
  • 74
    • 0037265516 scopus 로고    scopus 로고
    • Diketopiperazines in peptide and combinatorial chemistry
    • Fischer PM. Diketopiperazines in peptide and combinatorial chemistry. J. Pept. Sci. 2003; 9: 9-35.
    • (2003) J. Pept. Sci. , vol.9 , pp. 9-35
    • Fischer, P.M.1
  • 75
    • 0037156593 scopus 로고    scopus 로고
    • Recent advances in the synthesis of diketopiperazines
    • Dinsmore CJ, Bashore DC. Recent advances in the synthesis of diketopiperazines. Tetrahedron 2002; 58: 3297-3312.
    • (2002) Tetrahedron , vol.58 , pp. 3297-3312
    • Dinsmore, C.J.1    Bashore, D.C.2
  • 76
    • 0031000559 scopus 로고    scopus 로고
    • A simple procedure for the solid phase synthesis of diketopiperazines and diketomorpholine derivatives
    • Szardenings AK, Burkoth TS, Lu HH, Tien DW, Campbell DA. A simple procedure for the solid phase synthesis of diketopiperazines and diketomorpholine derivatives. Tetrahedron 1997; 53: 6573-6593.
    • (1997) Tetrahedron , vol.53 , pp. 6573-6593
    • Szardenings, A.K.1    Burkoth, T.S.2    Lu, H.H.3    Tien, D.W.4    Campbell, D.A.5
  • 78
    • 0037018444 scopus 로고    scopus 로고
    • A new resin-bound universal isonitrile for the Ugi CC reaction: Preparation and application to the synthesis of 2,5-diketopiperazines
    • Kennedy AL, Fryer AM, Josey JA. A new resin-bound universal isonitrile for the Ugi CC reaction: Preparation and application to the synthesis of 2,5-diketopiperazines. Org. Lett. 2002; 4: 1167-1170.
    • (2002) Org. Lett. , vol.4 , pp. 1167-1170
    • Kennedy, A.L.1    Fryer, A.M.2    Josey, J.A.3
  • 79
    • 0037078278 scopus 로고    scopus 로고
    • Cyclic dipeptides as building blocks for combination libraries Pt. 2. Synthesis of bifunctional diketopiperazines
    • Rodionov IL, Rodinova LN, Baidakova LK, Romashko AM, Balashova TA, Ivanov VT. Cyclic dipeptides as building blocks for combination libraries Pt. 2. Synthesis of bifunctional diketopiperazines. Tetrahedron 2002; 58: 8515-8523.
    • (2002) Tetrahedron , vol.58 , pp. 8515-8523
    • Rodionov, I.L.1    Rodinova, L.N.2    Baidakova, L.K.3    Romashko, A.M.4    Balashova, T.A.5    Ivanov, V.T.6
  • 81
    • 0033543486 scopus 로고    scopus 로고
    • Pseudo prolines in cyclic peptides. Conformational stabilisation of cyclo
    • [Pro-Thr(Ψ(Me,Me)Pro)-Pro]
    • Ruckle T, DeLavallez P, Keller M, Dumy P, Mutter M. Pseudo prolines in cyclic peptides. Conformational stabilisation of cyclo [Pro-Thr(Ψ(Me,Me)Pro)-Pro]. Tetrahedron 1999; 55: 11 281-11 288.
    • (1999) Tetrahedron. , vol.55 , pp. 11281-11288
    • Ruckle, T.1    DeLavallez, P.2    Keller, M.3    Dumy, P.4    Mutter, M.5
  • 83
    • 0035183462 scopus 로고    scopus 로고
    • Synthesis of cyclo β-tripeptides and their biological in vitro evaluation
    • Gademann K, Seebach D. Synthesis of cyclo β-tripeptides and their biological in vitro evaluation. Helv. Chim. Acta 2001; 84: 2924-2937.
    • (2001) Helv. Chim. Acta , vol.84 , pp. 2924-2937
    • Gademann, K.1    Seebach, D.2
  • 84
    • 0037460144 scopus 로고    scopus 로고
    • Conformationally homogeneous cyclic tetrapeptides: Useful new 3D-scaffolds
    • Glenn MP, Kelso MJ, Tyndall JDA, Fairlie DP. Conformationally homogeneous cyclic tetrapeptides: Useful new 3D-scaffolds. J. Am. Chem. Soc. 2003; 125: 640-641.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 640-641
    • Glenn, M.P.1    Kelso, M.J.2    Tyndall, J.D.A.3    Fairlie, D.P.4
  • 85
    • 0030999396 scopus 로고    scopus 로고
    • Cyclotetrapeptides and cyclopentapeptides: Occurrence and synthesis
    • Schmidt U, Langner J. Cyclotetrapeptides and cyclopentapeptides: Occurrence and synthesis. J. Pept. Res. 1997; 49: 67-73.
    • (1997) J. Pept. Res. , vol.49 , pp. 67-73
    • Schmidt, U.1    Langner, J.2
  • 87
    • 0026157219 scopus 로고
    • Conformation and formation tendency of the cyclotetrapeptide cyclo(D-Pro-D-Pro-L-Pro-L-Pro): Experimental results and molecular modelling studies
    • Maestle W, Link U, Thewalt U, Weber T, Rothe M. Conformation and formation tendency of the cyclotetrapeptide cyclo(D-Pro-D-Pro-L-Pro-L-Pro): Experimental results and molecular modelling studies. Biopolymers 1991; 31: 735-744.
    • (1991) Biopolymers , vol.31 , pp. 735-744
    • Maestle, W.1    Link, U.2    Thewalt, U.3    Weber, T.4    Rothe, M.5
  • 88
    • 0000477615 scopus 로고
    • Prediction of the best linear precursor in the synthesis of cyclotetrapeptides by molecular mechanics calculations
    • Cavalier-Frontin F, Pèpe G, Verducci J, Siri D, Jacquier R. Prediction of the best linear precursor in the synthesis of cyclotetrapeptides by molecular mechanics calculations. J. Am. Chem. Soc. 1992; 114: 8885-8890.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 8885-8890
    • Cavalier-Frontin, F.1    Pèpe, G.2    Verducci, J.3    Siri, D.4    Jacquier, R.5
  • 89
  • 92
  • 93
  • 94
    • 0035991443 scopus 로고    scopus 로고
    • Synthesis of cyclopentapeptides and cycloheptapeptides by DEPBT and the influence of some factors on cyclisation
    • Tang YC, Xie HB, Tian GL, Ye YH. Synthesis of cyclopentapeptides and cycloheptapeptides by DEPBT and the influence of some factors on cyclisation. J. Pept. Res. 2002; 60: 95-103.
    • (2002) J. Pept. Res. , vol.60 , pp. 95-103
    • Tang, Y.C.1    Xie, H.B.2    Tian, G.L.3    Ye, Y.H.4
  • 95
    • 0035993828 scopus 로고    scopus 로고
    • Studies on the synthesis of cyclic pentapeptides as LHRH antagonists and the factors that influence cyclisation yield
    • Gao XM, Ye YH, Bernd M, Kutscher B. Studies on the synthesis of cyclic pentapeptides as LHRH antagonists and the factors that influence cyclisation yield. J. Pept. Sci. 2002; 8: 418-430.
    • (2002) J. Pept. Sci. , vol.8 , pp. 418-430
    • Gao, X.M.1    Ye, Y.H.2    Bernd, M.3    Kutscher, B.4
  • 98
    • 0026557408 scopus 로고
    • Cyclic hexapeptides derived from the human thymopoietin III
    • Kessler H, Haase B. Cyclic hexapeptides derived from the human thymopoietin III. Int. J. Pept. Protein Res. 1992; 39: 36-40.
    • (1992) Int. J. Pept. Protein Res. , vol.39 , pp. 36-40
    • Kessler, H.1    Haase, B.2
  • 100
    • 0028283014 scopus 로고
    • Synthesis of cyclic pentapeptides and hexapeptides - A general synthetic strategy on DAS resin
    • Sowemimo V, Scanlon D, Jones P, Craik DJ. Synthesis of cyclic pentapeptides and hexapeptides - a general synthetic strategy on DAS resin. J. Protein Chem. 1994; 13: 339-346.
    • (1994) J. Protein Chem. , vol.13 , pp. 339-346
    • Sowemimo, V.1    Scanlon, D.2    Jones, P.3    Craik, D.J.4
  • 103
    • 0029967644 scopus 로고    scopus 로고
    • A new cyclic heptapeptide from marine sponge Hymeniacidin sp
    • Kobayashi J, Nakamura T, Tsuda M. Hymenamide F, a new cyclic heptapeptide from marine sponge Hymeniacidin sp. Tetrahedron 1996; 52: 6355-6360.
    • (1996) Tetrahedron. , vol.52 , pp. 6355-6360
    • Kobayashi, J.1    Nakamura, T.2    Tsuda, M.3    Hymenamide, F.4
  • 105
    • 0030873355 scopus 로고    scopus 로고
    • Cyclic heptapeptides axinastatins 2, 3 and 4. Conformational analysis and biological potential
    • Mechnich O, Hessler G, Kessler H, Bernd M, Kutscher B. Cyclic heptapeptides axinastatins 2, 3 and 4. Conformational analysis and biological potential. Helv. Chim. Acta 1997; 80: 1338-1354.
    • (1997) Helv. Chim. Acta , vol.80 , pp. 1338-1354
    • Mechnich, O.1    Hessler, G.2    Kessler, H.3    Bernd, M.4    Kutscher, B.5
  • 108
    • 0031550593 scopus 로고    scopus 로고
    • Conformation of cyclic heptapeptides. Solid and solution state conformation of yunnanin A
    • Morita H, Kayashita T, Takeya K, Itokawa H, Shiro M. Conformation of cyclic heptapeptides. Solid and solution state conformation of yunnanin A. Tetrahedron 1997; 53: 1607-1616.
    • (1997) Tetrahedron. , vol.53 , pp. 1607-1616
    • Morita, H.1    Kayashita, T.2    Takeya, K.3    Itokawa, H.4    Shiro, M.5
  • 109
    • 0028786813 scopus 로고
    • Crystal and solution structure of cycloheptapeptide pseudostellarin D
    • Morita H, Kayashita T, Takeya K, Itokawa H, Shiro M. Crystal and solution structure of cycloheptapeptide pseudostellarin D. Tetrahedron 1995; 51: 12 539-12 548.
    • (1995) Tetrahedron. , vol.51 , pp. 12539-12548
    • Morita, H.1    Kayashita, T.2    Takeya, K.3    Itokawa, H.4    Shiro, M.5
  • 113
    • 15844411955 scopus 로고    scopus 로고
    • Aciculitins A-C: Cytotoxic and antifungal cyclic peptides from the sponge Aciculites orientalis
    • Bewley CA, He H, Williams DH, Faulkner DJ. Aciculitins A-C: Cytotoxic and antifungal cyclic peptides from the sponge Aciculites orientalis. J. Am. Chem. Soc. 1996; 118: 4314-4321.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 4314-4321
    • Bewley, C.A.1    He, H.2    Williams, D.H.3    Faulkner, D.J.4
  • 115
    • 0029874164 scopus 로고    scopus 로고
    • Cycloleonuripeptides A, B, and C, three new Pro-rich cyclic nonapeptides from Leonurus heterophyllus
    • Morita H, Gonda A, Takeya K, Itokawa H. Cycloleonuripeptides A, B, and C, three new Pro-rich cyclic nonapeptides from Leonurus heterophyllus. Bioorg. Med. Chem. Lett. 1996; 6: 767-770.
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 767-770
    • Morita, H.1    Gonda, A.2    Takeya, K.3    Itokawa, H.4
  • 116
    • 0031172315 scopus 로고    scopus 로고
    • Cyclic octapeptides from Stellaria dichotoma var. Lanceolata
    • Morita H, Takeya K, Itokawa H. Cyclic octapeptides from Stellaria dichotoma var. Lanceolata. Phytochemistry 1997; 45: 841-845.
    • (1997) Phytochemistry , vol.45 , pp. 841-845
    • Morita, H.1    Takeya, K.2    Itokawa, H.3
  • 117
    • 0033952824 scopus 로고    scopus 로고
    • Synthesis of the marine sponge cycloheptapeptide phakellistatin 5
    • Pettit GR, Toki BE, Xu JP, Brune DC. Synthesis of the marine sponge cycloheptapeptide phakellistatin 5. J. Nat. Prod. 2000; 63: 22-28.
    • (2000) J. Nat. Prod. , vol.63 , pp. 22-28
    • Pettit, G.R.1    Toki, B.E.2    Xu, J.P.3    Brune, D.C.4
  • 118
    • 0032916413 scopus 로고    scopus 로고
    • Synthesis of the Indian Ocean marine sponge cycloheptapeptide phakellistatin 2
    • Pettit GR, Rhodes MR, Tan R. Synthesis of the Indian Ocean marine sponge cycloheptapeptide phakellistatin 2. J. Nat. Prod. 1999; 62: 409-414.
    • (1999) J. Nat. Prod. , vol.62 , pp. 409-414
    • Pettit, G.R.1    Rhodes, M.R.2    Tan, R.3
  • 121
    • 0031900379 scopus 로고    scopus 로고
    • Synthesis and stereochemistry of axinastatin 4
    • Bates RB, Caldera S, Ruane MD. Synthesis and stereochemistry of axinastatin 4. J. Nat. Prod. 1998; 61: 405-405.
    • (1998) J. Nat. Prod. , vol.61 , pp. 405
    • Bates, R.B.1    Caldera, S.2    Ruane, M.D.3
  • 122
  • 123
    • 0001341309 scopus 로고    scopus 로고
    • Synthesis of nanotube-forming cyclic octapeptides via a Fmoc-strategy
    • Polaskava ME, Ede NJ, Lambert JN. Synthesis of nanotube-forming cyclic octapeptides via a Fmoc-strategy. Aust. J. Chem. 1998; 51: 535-540.
    • (1998) Aust. J. Chem. , vol.51 , pp. 535-540
    • Polaskava, M.E.1    Ede, N.J.2    Lambert, J.N.3
  • 124
    • 0001097082 scopus 로고    scopus 로고
    • A pair of pyrene groups as a conformational probe for antiparallel β-sheet structure formed in cyclic peptides
    • Mihara N, Hayashida J, Hasegawa H, Ogawa HI, Fujimoto T, Nishino N. A pair of pyrene groups as a conformational probe for antiparallel β-sheet structure formed in cyclic peptides. J. Chem Soc. Trans 2 1997; 517-522.
    • (1997) J. Chem. Soc. Trans. , vol.2 , pp. 517-522
    • Mihara, N.1    Hayashida, J.2    Hasegawa, H.3    Ogawa, H.I.4    Fujimoto, T.5    Nishino, N.6
  • 125
    • 0027754031 scopus 로고
    • Direct formation of the antibiotic gramicidin S from pentapeptide active esters having no protection on the Orn side-chain
    • Tamaki M, Akabori S, Muramatsu I. Direct formation of the antibiotic gramicidin S from pentapeptide active esters having no protection on the Orn side-chain. J. Am. Chem. Soc. 1993; 115: 10 492-10 496.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10492-10496
    • Tamaki, M.1    Akabori, S.2    Muramatsu, I.3
  • 126
    • 0027759387 scopus 로고
    • CD spectra and cyclisation of linear pentapeptides as gramicidin S precursors with Orn(Z)
    • Tamaki M, Akabori S, Muramatsu I. CD spectra and cyclisation of linear pentapeptides as gramicidin S precursors with Orn(Z). Bull Chem. Soc. Jpn 1993; 66: 3113-3115.
    • (1993) Bull. Chem. Soc. Jpn. , vol.66 , pp. 3113-3115
    • Tamaki, M.1    Akabori, S.2    Muramatsu, I.3
  • 128
  • 132
    • 0033546090 scopus 로고    scopus 로고
    • Amino acid side-chain attachment approach and its application to the synthesis of Tyr-containing cyclic peptides
    • Cabrele C, Langer M, Beck-Sickinger AG. Amino acid side-chain attachment approach and its application to the synthesis of Tyr-containing cyclic peptides. J. Org. Chem. 1999; 64: 4353-4361.
    • (1999) J. Org. Chem. , vol.64 , pp. 4353-4361
    • Cabrele, C.1    Langer, M.2    Beck-Sickinger, A.G.3
  • 135
    • 0030925342 scopus 로고    scopus 로고
    • Solid phase synthesis of cyclosporine analogues
    • Ko SY, Wenger RM. Solid phase synthesis of cyclosporine analogues. Helv. Chim. Acta 1997; 80: 695-705.
    • (1997) Helv. Chim. Acta , vol.80 , pp. 695-705
    • Ko, S.Y.1    Wenger, R.M.2
  • 137
    • 0342656979 scopus 로고    scopus 로고
    • Total synthesis of cyclosporin O both in solution and solid phase, using coupling reagents BEMT, BDMP and BEP
    • Li P, Xu JC. Total synthesis of cyclosporin O both in solution and solid phase, using coupling reagents BEMT, BDMP and BEP. J. Org. Chem. 2000; 65: 2951-2958.
    • (2000) J. Org. Chem. , vol.65 , pp. 2951-2958
    • Li, P.1    Xu, J.C.2
  • 138
    • 0037043020 scopus 로고    scopus 로고
    • Triphosgene as highly efficient reagent for the solid phase coupling of N-alkylated amino acids - Total synthesis of cyclosporin O
    • Thern B, Rudolph J, Jung G. Triphosgene as highly efficient reagent for the solid phase coupling of N-alkylated amino acids - total synthesis of cyclosporin O. Tetrahedron Lett. 2002; 43: 5013-5016.
    • (2002) Tetrahedron. Lett. , vol.43 , pp. 5013-5016
    • Thern, B.1    Rudolph, J.2    Jung, G.3
  • 139
    • 0034470558 scopus 로고    scopus 로고
    • Combinatorial biomimetic chemistry: Parallel synthesis of a small library of β-hairpin mimetics based on loop III from human platelet-derived growth factor B
    • Jiang L, Moehle K, Dhanapal B, Obrecht D, Robinson JA. Combinatorial biomimetic chemistry: parallel synthesis of a small library of β-hairpin mimetics based on loop III from human platelet-derived growth factor B. Helv. Chim. Acta 2000; 83: 3097-3112.
    • (2000) Helv. Chim. Acta , vol.83 , pp. 3097-3112
    • Jiang, L.1    Moehle, K.2    Dhanapal, B.3    Obrecht, D.4    Robinson, J.A.5
  • 140
    • 0002632421 scopus 로고    scopus 로고
    • Assembly of cyclic peptide dendrimers from unprotected linear building blocks in aqueous solution
    • Pallin TD, Tam JP. Assembly of cyclic peptide dendrimers from unprotected linear building blocks in aqueous solution. J. Chem. Soc. Chem. Comm. 1996; 1345-1346.
    • (1996) J. Chem. Soc. Chem. Comm. , pp. 1345-1346
    • Pallin, T.D.1    Tam, J.P.2
  • 141
    • 0029904934 scopus 로고    scopus 로고
    • Cyclic peptides from linear unprotected peptide precursors through thiazolidine formation
    • Botti P, Pallin TD, Tam JP. Cyclic peptides from linear unprotected peptide precursors through thiazolidine formation. J. Am. Chem. Soc. 1996; 118: 10 018-10 024.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 10018-10024
    • Botti, P.1    Pallin, T.D.2    Tam, J.P.3
  • 142
    • 0030590456 scopus 로고    scopus 로고
    • Analogues of oxytocin with an oxime bridge using chemoselectively addressable building blocks
    • Wahl F, Mutter M. Analogues of oxytocin with an oxime bridge using chemoselectively addressable building blocks. Tetrahedron Lett. 1996; 37: 6861-6864.
    • (1996) Tetrahedron. Lett. , vol.37 , pp. 6861-6864
    • Wahl, F.1    Mutter, M.2
  • 143
    • 0001447789 scopus 로고
    • 3rd. edn, Neurath H, Hill RL (eds). Academic Press: New York
    • Ovchinnikov YA, Ivanov VT. In Proteins, 3rd edn, Neurath H, Hill RL (eds). Academic Press: New York, 1982; 3: 307.
    • (1982) Proteins , vol.3 , pp. 307
    • Ovchinnikov, Y.A.1    Ivanov, V.T.2
  • 145
    • 0344241060 scopus 로고    scopus 로고
    • A general methodology for automated solid phase synthesis of depsides and depsipeptides. Preparation of a valinomycin analogue
    • Kuisle O, Quinoá E, Riguero R. A general methodology for automated solid phase synthesis of depsides and depsipeptides. Preparation of a valinomycin analogue. J. Org. Chem. 1999; 64: 8063-8075.
    • (1999) J. Org. Chem. , vol.64 , pp. 8063-8075
    • Kuisle, O.1    Quinoá, E.2    Riguero, R.3
  • 146
    • 0034809667 scopus 로고    scopus 로고
    • Total synthesis and biological investigations of tamandarins A and B and analogue
    • Liang B, Richard DJ, Portonovo P, Joullie MM. Total synthesis and biological investigations of tamandarins A and B and analogue. J. Am. Chem. Soc. 2001; 123: 4469-4474.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 4469-4474
    • Liang, B.1    Richard, D.J.2    Portonovo, P.3    Joullie, M.M.4
  • 147
    • 0031045880 scopus 로고    scopus 로고
    • Total synthesis of dehydrodidemnin B. Use of uronium and phosphonium salt coupling reagents in peptide synthesis in solution
    • and syntheses refs. cited therein
    • Jou G, González I, Albericio F, Lloyd-Williams P, Giralt E. Total synthesis of dehydrodidemnin B. Use of uronium and phosphonium salt coupling reagents in peptide synthesis in solution. J. Org. Chem. 1997; 62: 354-366 and syntheses refs. cited therein.
    • (1997) J. Org. Chem. , vol.62 , pp. 354-366
    • Jou, G.1    González, I.2    Albericio, F.3    Lloyd-Williams, P.4    Giralt, E.5
  • 148
    • 0035935126 scopus 로고    scopus 로고
    • Synthesis of hapalosin analogues by solid phase assembly of acyclic precursors
    • Hermann C, Giammasi C, Geyer A, Maier ME. Synthesis of hapalosin analogues by solid phase assembly of acyclic precursors. Tetrahedron 2001; 57: 8999-9010.
    • (2001) Tetrahedron. , vol.57 , pp. 8999-9010
    • Hermann, C.1    Giammasi, C.2    Geyer, A.3    Maier, M.E.4
  • 151
    • 0030951560 scopus 로고    scopus 로고
    • Analogues incorporating trans 4-hydroxyproline that reverse multidrug resistance better than hapalosin
    • Dinh TQ, Smith CD, Armstrong RW. Analogues incorporating trans 4-hydroxyproline that reverse multidrug resistance better than hapalosin. J. Org Chem. 1997; 62: 790-791.
    • (1997) J. Org Chem. , vol.62 , pp. 790-791
    • Dinh, T.Q.1    Smith, C.D.2    Armstrong, R.W.3
  • 152
    • 0029920444 scopus 로고    scopus 로고
    • Destruxin analogues: Depsipeptidic bond replacement by amide bond
    • Cavalier F, Jacquier R, Mercadier J-L, Verducci J. Destruxin analogues: depsipeptidic bond replacement by amide bond. Tetrahedron 1996; 52: 6173-6186.
    • (1996) Tetrahedron. , vol.52 , pp. 6173-6186
    • Cavalier, F.1    Jacquier, R.2    Mercadier, J.-L.3    Verducci, J.4
  • 153
    • 0031021498 scopus 로고    scopus 로고
    • Synthesis of host-selective phytoxin destruxin B avoiding diketopiperazine formation from an N-methyl amino acid dipeptide by use of Boc-hydrazide derivative
    • Ward DE, Lazny R, Pedras MSC. Synthesis of host-selective phytoxin destruxin B avoiding diketopiperazine formation from an N-methyl amino acid dipeptide by use of Boc-hydrazide derivative. Tetrahedron Lett. 1997; 38: 339-342.
    • (1997) Tetrahedron. Lett. , vol.38 , pp. 339-342
    • Ward, D.E.1    Lazny, R.2    Pedras, M.S.C.3
  • 154
    • 0035900345 scopus 로고    scopus 로고
    • Probing host-selective phytotoxicity: Synthesis of destruxin B and several natural analogues
    • Ward DE, Gai YZ, Lazny R, Pedras MSC. Probing host-selective phytotoxicity: synthesis of destruxin B and several natural analogues. J. Org. Chem. 2001; 66: 7832-7840.
    • (2001) J. Org. Chem. , vol.66 , pp. 7832-7840
    • Ward, D.E.1    Gai, Y.Z.2    Lazny, R.3    Pedras, M.S.C.4
  • 157
    • 0033588189 scopus 로고    scopus 로고
    • Total synthesis of cryptophycins-l,-3,-4 and -24 (arenastatin A) and -29, cytotoxic depsipeptides from cyanobacteria of the nostocacae
    • and refs. cited therein
    • White JD, Hong J, Robarge LA. Total synthesis of cryptophycins-l,-3,-4 and -24 (arenastatin A) and -29, cytotoxic depsipeptides from cyanobacteria of the nostocacae. J. Org. Chem. 1999; 64: 6206-6216 and refs. cited therein.
    • (1999) J. Org. Chem. , vol.64 , pp. 6206-6216
    • White, J.D.1    Hong, J.2    Robarge, L.A.3
  • 158
    • 0035939469 scopus 로고    scopus 로고
    • Studies directed towards the synthesis of stevastelins - A macrolactonisation approach to stevastelin B
    • Chakraborty TK, Ghosh S, Dutta S. Studies directed towards the synthesis of stevastelins - a macrolactonisation approach to stevastelin B. Tetrahedron Lett. 2001; 42: 5085-5088.
    • (2001) Tetrahedron. Lett. , vol.42 , pp. 5085-5088
    • Chakraborty, T.K.1    Ghosh, S.2    Dutta, S.3
  • 159
    • 0023831121 scopus 로고
    • A convergent enantiospecific total synthesis of the novel cyclodepsipeptide (+) jasplakinolide (jaspamide)
    • Grieco PA, Hon YS, Perez-Medrano A. A convergent enantiospecific total synthesis of the novel cyclodepsipeptide (+) jasplakinolide (jaspamide). J. Am. Chem. Soc. 1988; 110: 1630-1631.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 1630-1631
    • Grieco, P.A.1    Hon, Y.S.2    Perez-Medrano, A.3
  • 160
    • 0025819848 scopus 로고
    • Asymmetric total synthesis of (+) jasplakinolide
    • Chu KS, Negrete GR, Konopelski JP. Asymmetric total synthesis of (+) jasplakinolide. J. Org. Chem. 1991; 56: 5196-5202.
    • (1991) J. Org. Chem. , vol.56 , pp. 5196-5202
    • Chu, K.S.1    Negrete, G.R.2    Konopelski, J.P.3
  • 161
    • 33645672005 scopus 로고
    • Total synthesis of geodiamolide A - A novel cyclodepsipeptide of marine origin
    • White JD, Amedio JC. Total synthesis of geodiamolide A - a novel cyclodepsipeptide of marine origin. J. Org Chem. 1989; 54: 736-738.
    • (1989) J. Org. Chem. , vol.54 , pp. 736-738
    • White, J.D.1    Amedio, J.C.2
  • 162
    • 0027931069 scopus 로고
    • Total synthesis of doliculide, a potent cytotoxic cyclodepsipeptide from the Japanese sea hare Dolabella auricularia
    • Ishiwata H, Sone H, Kigoshi H, Yamada K. Total synthesis of doliculide, a potent cytotoxic cyclodepsipeptide from the Japanese sea hare Dolabella auricularia. J. Org. Chem. 1994; 59: 4712-4713.
    • (1994) J. Org. Chem. , vol.59 , pp. 4712-4713
    • Ishiwata, H.1    Sone, H.2    Kigoshi, H.3    Yamada, K.4
  • 163
    • 0035901366 scopus 로고    scopus 로고
    • Synthesis of conformationally restricted cyclic pentadepsipeptides via direct amide cyclisations
    • Koch KN, Linden A, Heimgartner H. Synthesis of conformationally restricted cyclic pentadepsipeptides via direct amide cyclisations. Tetrahedron 2001; 57: 2311-2326.
    • (2001) Tetrahedron. , vol.57 , pp. 2311-2326
    • Koch, K.N.1    Linden, A.2    Heimgartner, H.3
  • 165
    • 0034618203 scopus 로고    scopus 로고
    • Synthesis and evaluation of hapalosin and analogs as MDR-reversing agents
    • Boger DL, Chen Y, Foster CA. Synthesis and evaluation of hapalosin and analogs as MDR-reversing agents. Bioorg. Med. Chem. Lett. 2000; 10: 1741-1744.
    • (2000) Bioorg. Med. Chem. Lett. , vol.10 , pp. 1741-1744
    • Boger, D.L.1    Chen, Y.2    Foster, C.A.3
  • 170
    • 0035932040 scopus 로고    scopus 로고
    • Total synthesis of antitumour depsipeptide (-)- doliculide
    • Ghosh AK, Liu CF. Total synthesis of antitumour depsipeptide (-)- doliculide. Org. Lett. 2001; 3: 635-638.
    • (2001) Org. Lett. , vol.3 , pp. 635-638
    • Ghosh, A.K.1    Liu, C.F.2
  • 171
    • 0029798902 scopus 로고    scopus 로고
    • Conformational control by thiazole and oxazoline rings in cyclic octapeptides of marine origin. Novel macrocyclic chair and boat conformation
    • Abbenante G, Fairlie DP, Gahan LR, Hanson GR, Pierens GK, van den Brank AL. Conformational control by thiazole and oxazoline rings in cyclic octapeptides of marine origin. Novel macrocyclic chair and boat conformation. J. Am Chem. Soc. 1996; 118: 10 384-10 388.
    • (1996) J. Am Chem. Soc. , vol.118 , pp. 10384-10388
    • Abbenante, G.1    Fairlie, D.P.2    Gahan, L.R.3    Hanson, G.R.4    Pierens, G.K.5    van den Brank, A.L.6
  • 172
    • 0000314051 scopus 로고
    • Synthetic studies of biologically active marine cyclopeptides
    • Wipf P. Synthetic studies of biologically active marine cyclopeptides. Chem. Rev. 1995; 95: 2115-2134.
    • (1995) Chem. Rev. , vol.95 , pp. 2115-2134
    • Wipf, P.1
  • 173
    • 0035124856 scopus 로고    scopus 로고
    • Efficient syntheses of biologically active peptides of aquatic origin involving unusual amino acids
    • Shioiri T, Hamada Y. Efficient syntheses of biologically active peptides of aquatic origin involving unusual amino acids. Synlett 2001; 184-201.
    • (2001) Synlett. , pp. 184-201
    • Shioiri, T.1    Hamada, Y.2
  • 175
    • 0034712229 scopus 로고    scopus 로고
    • Total synthesis and revision of stereochemistry of the marine metabolite trunkamide A
    • Wipf P, Uto Y. Total synthesis and revision of stereochemistry of the marine metabolite trunkamide A. J. Org. Chem. 2000; 65: 1037-1049.
    • (2000) J. Org. Chem. , vol.65 , pp. 1037-1049
    • Wipf, P.1    Uto, Y.2
  • 176
    • 0035953040 scopus 로고    scopus 로고
    • Total synthesis of the prenylated cyclopeptide trunkamide A, a cytotoxic metabolite from Lissoclinum sp
    • McKeever B, Pattenden G. Total synthesis of the prenylated cyclopeptide trunkamide A, a cytotoxic metabolite from Lissoclinum sp. Tetrahedron Lett. 2001; 42: 2573-2577.
    • (2001) Tetrahedron. Lett. , vol.42 , pp. 2573-2577
    • McKeever, B.1    Pattenden, G.2
  • 178
    • 0035208484 scopus 로고    scopus 로고
    • Synthesis and metal-templated assembly of oxazole and thiazole-based amino acids. Total synthesis of nostacyclamide and related cyclic peptides
    • Bertram A, Pattenden G. Synthesis and metal-templated assembly of oxazole and thiazole-based amino acids. Total synthesis of nostacyclamide and related cyclic peptides. Synlett 2001; 1873-1874.
    • (2001) Synlett. , pp. 1873-1874
    • Bertram, A.1    Pattenden, G.2
  • 179
    • 0035906488 scopus 로고    scopus 로고
    • Total synthesis of dendroamide A, a novel cyclic peptide that reverses multiple drug resistance
    • Xia Z, Smith CD. Total synthesis of dendroamide A, a novel cyclic peptide that reverses multiple drug resistance. J. Org. Chem. 2001; 66: 3459-3466.
    • (2001) J. Org. Chem. , vol.66 , pp. 3459-3466
    • Xia, Z.1    Smith, C.D.2
  • 180
    • 0034977432 scopus 로고    scopus 로고
    • Total synthesis of cis,cis-ceratospongamide, a bioactive thiazole-containing cyclic peptide from marine origin
    • Yokokawa F, Sameshima H, Shioiri T. Total synthesis of cis,cis-ceratospongamide, a bioactive thiazole-containing cyclic peptide from marine origin. Synlett 2001: 986-988.
    • (2001) Synlett. , pp. 986-988
    • Yokokawa, F.1    Sameshima, H.2    Shioiri, T.3
  • 181
    • 0035908266 scopus 로고    scopus 로고
    • Total synthesis of lyngbyabellin A, a potent cytotoxic metabolite from the cyanobacterium Lyngbya majuscula
    • Yokokawa F, Sameshima H, Shioiri T. Total synthesis of lyngbyabellin A, a potent cytotoxic metabolite from the cyanobacterium Lyngbya majuscula. Tetrahedron Lett. 2001; 42: 4171-4174.
    • (2001) Tetrahedron. Lett. , vol.42 , pp. 4171-4174
    • Yokokawa, F.1    Sameshima, H.2    Shioiri, T.3
  • 184
    • 0034696498 scopus 로고    scopus 로고
    • Total synthesis and assignment of configuration of the thiazole-based cyclopeptide cyclodidemnamide isolated from sea squirt Didemnin molle
    • Boden CDJ, Norley M, Pattenden G. Total synthesis and assignment of configuration of the thiazole-based cyclopeptide cyclodidemnamide isolated from sea squirt Didemnin molle. J. Chem Soc. Perkin Trans. 1 2000; 883-888.
    • (2000) J. Chem Soc. Perkin. Trans. , vol.1 , pp. 883-888
    • Boden, C.D.J.1    Norley, M.2    Pattenden, G.3
  • 185
    • 0034696496 scopus 로고    scopus 로고
    • Total synthesis and reassignment of configuration of the cyclopeptides lissoclinamides 4 and 5 from Lissoclinum patella
    • Boden CDJ, Pattenden G. Total synthesis and reassignment of configuration of the cyclopeptides lissoclinamides 4 and 5 from Lissoclinum patella. J. Chem. Soc. Perkin Trans I 2000; 875-882.
    • (2000) J. Chem. Soc. Perkin. Trans. I , pp. 875-882
    • Boden, C.D.J.1    Pattenden, G.2
  • 186
    • 0032764171 scopus 로고    scopus 로고
    • Total synthesis of macrocyclic antibiotic, micrococcin P
    • Okumura K, Nakamura Y, Shin C-g. Total synthesis of macrocyclic antibiotic, micrococcin P. Bull. Chem. Soc. Jpn 1999; 72: 1561-1569.
    • (1999) Bull. Chem. Soc. Jpn. , vol.72 , pp. 1561-1569
    • Okumura, K.1    Nakamura, Y.2    Shin, C.-G.3
  • 188
    • 0033570154 scopus 로고    scopus 로고
    • Synthesis of dolastatin 1, a cytotoxic cyclic hexapeptide from the sea hare Dolabella auricularia
    • Yamada S, Kigoshi H. Synthesis of dolastatin 1, a cytotoxic cyclic hexapeptide from the sea hare Dolabella auricularia. Tetrahedron 1999; 55: 12 301-12 308.
    • (1999) Tetrahedron. , vol.55 , pp. 12301-12308
    • Yamada, S.1    Kigoshi, H.2
  • 189
    • 0033601447 scopus 로고    scopus 로고
    • Total synthesis of mollamide, a reverse prenyl substituted cytotoxic cyclic peptide from Didemnum molle
    • McKeever B, Pattenden G. Total synthesis of mollamide, a reverse prenyl substituted cytotoxic cyclic peptide from Didemnum molle. Tetrahedron Lett. 1999; 40: 9317-9320.
    • (1999) Tetrahedron. Lett. , vol.40 , pp. 9317-9320
    • McKeever, B.1    Pattenden, G.2
  • 192
    • 0031597449 scopus 로고    scopus 로고
    • Total synthesis of oxazole-based virginiamycin antibiotics 14,15 anhydro pristinamycin IIB
    • Entwistle DA, Jordan SI, Montgomery J, Pattenden G. Total synthesis of oxazole-based virginiamycin antibiotics 14,15 anhydro pristinamycin IIB. Synthesis 1998; 603-612.
    • (1998) Synthesis , pp. 603-612
    • Entwistle, D.A.1    Jordan, S.I.2    Montgomery, J.3    Pattenden, G.4
  • 193
    • 0030458540 scopus 로고    scopus 로고
    • Total synthesis and assignment of configuration of lissoclinamide 7
    • Wipf P, Fritch PC. Total synthesis and assignment of configuration of lissoclinamide 7. J. Am. Chem. Soc. 1996; 118: 12 358-12 367.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 12358-12367
    • Wipf, P.1    Fritch, P.C.2
  • 194
    • 0032516335 scopus 로고    scopus 로고
    • Total synthesis and assignment of stereochemistry of raocyclamide, cyclopeptide from cyanobacterium Oscillatoria rao
    • Freeman DJ, Pattenden G. Total synthesis and assignment of stereochemistry of raocyclamide, cyclopeptide from cyanobacterium Oscillatoria rao. Tetrahedron Lett. 1998; 39: 3251-3254.
    • (1998) Tetrahedron. Lett. , vol.39 , pp. 3251-3254
    • Freeman, D.J.1    Pattenden, G.2
  • 195
    • 0035905352 scopus 로고    scopus 로고
    • Synthesis of nominal diazonamides Pt 1. Convergent preparation of the structure proposed for (-)-diazonamide A
    • Li J, Jeong S, Esser L, Harran PG. Synthesis of nominal diazonamides Pt 1. Convergent preparation of the structure proposed for (-)-diazonamide A. Angew. Chem. Int. Ed. 2001; 40: 4765-4770.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 4765-4770
    • Li, J.1    Jeong, S.2    Esser, L.3    Harran, P.G.4
  • 196
    • 0035905532 scopus 로고    scopus 로고
    • Total synthesis of nominal diazonamides Part 2. On the true structure and origin of natural isolates
    • Li J, Burgett ANG, Esser L, Amezcua C, Harran PG. Total synthesis of nominal diazonamides Part 2. On the true structure and origin of natural isolates. Angew. Chem. Int. Ed. 2001; 40: 4770-4773.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 4770-4773
    • Li, J.1    Burgett, A.N.G.2    Esser, L.3    Amezcua, C.4    Harran, P.G.5
  • 199
    • 0032538360 scopus 로고    scopus 로고
    • Nonconventional stereochemical issues in the design of the synthesis of vancomycin antibiotics: Challenges imposed by axial and non-planar chiral elements in the heptapeptide aglycones
    • Evans DA, Dinsmore CJ, Watson PS, Wood MR, Richardson TI, Trotter BW, Katz JL. Nonconventional stereochemical issues in the design of the synthesis of vancomycin antibiotics: Challenges imposed by axial and non-planar chiral elements in the heptapeptide aglycones. Angew. Chem. Int. Ed. 1998; 37: 2704-2708.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2704-2708
    • Evans, D.A.1    Dinsmore, C.J.2    Watson, P.S.3    Wood, M.R.4    Richardson, T.I.5    Trotter, B.W.6    Katz, J.L.7
  • 205
    • 0033531677 scopus 로고    scopus 로고
    • Diastereoselective total synthesis of the vancomycin aglycone with ordered atropisomer equilibrations
    • Boger DL, Miyazaki S, Kim SH, Wu JH, Loiseleur O, Castle SL. Diastereoselective total synthesis of the vancomycin aglycone with ordered atropisomer equilibrations. J. Am. Chem. Soc. 1999; 121: 3226-3227.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 3226-3227
    • Boger, D.L.1    Miyazaki, S.2    Kim, S.H.3    Wu, J.H.4    Loiseleur, O.5    Castle, S.L.6
  • 207
    • 0034885143 scopus 로고    scopus 로고
    • Vancomycin, teicoplanin and ramoplanin: Synthetic and mechanistic studies
    • Boger DL. Vancomycin, teicoplanin and ramoplanin: synthetic and mechanistic studies. Med. Res. Rev. 2001; 21: 356-381.
    • (2001) Med. Res. Rev. , vol.21 , pp. 356-381
    • Boger, D.L.1
  • 208
    • 0030998926 scopus 로고    scopus 로고
    • Synthesis of (9R, 12S)- and (9S, 12S)-cycloisodityrosine and their N-methyl derivatives
    • Boger DL, Zhou J, Borzilleri RM, Nukii S, Castle SL. Synthesis of (9R, 12S)- and (9S, 12S)-cycloisodityrosine and their N-methyl derivatives. J. Org. Chem. 1997; 62: 2054-2069.
    • (1997) J. Org. Chem. , vol.62 , pp. 2054-2069
    • Boger, D.L.1    Zhou, J.2    Borzilleri, R.M.3    Nukii, S.4    Castle, S.L.5
  • 211
    • 0001904789 scopus 로고    scopus 로고
    • Lantibiotics and microcins: Novel post-translational modifications of polypeptides
    • Kaiser D, Jack RW, Jung G. Lantibiotics and microcins: novel post-translational modifications of polypeptides. Pure Appl. Chem. 1998; 70: 97-104.
    • (1998) Pure Appl. Chem. , vol.70 , pp. 97-104
    • Kaiser, D.1    Jack, R.W.2    Jung, G.3
  • 214
    • 0030837553 scopus 로고    scopus 로고
    • A refined model for the somatostatin pharmacophore: Conformational analysis of lanthionine-sandostatin analogues
    • Melacini G, Zhu Q, Ösapay G, Goodman M. A refined model for the somatostatin pharmacophore: Conformational analysis of lanthionine-sandostatin analogues. J. Med. Chem. 1997; 40: 2252-2258.
    • (1997) J. Med. Chem. , vol.40 , pp. 2252-2258
    • Melacini, G.1    Zhu, Q.2    Ösapay, G.3    Goodman, M.4
  • 218
    • 0033576637 scopus 로고    scopus 로고
    • Rolling loop scan: An approach featuring ring-closing metathesis for generating libraries of peptides with molecular shapes mimicking bioactive conformations or local folding of peptides and proteins
    • and ref. cited therein
    • Reichwein JF, Wels B, Kruijtzer JAW, Versluis C, Liskamp RMJ. Rolling loop scan: An approach featuring ring-closing metathesis for generating libraries of peptides with molecular shapes mimicking bioactive conformations or local folding of peptides and proteins. Angew. Chem. Int. Ed. 1999; 38: 3684-3687, and ref. cited therein.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 3684-3687
    • Reichwein, J.F.1    Wels, B.2    Kruijtzer, J.A.W.3    Versluis, C.4    Liskamp, R.M.J.5
  • 219
    • 0037423987 scopus 로고    scopus 로고
    • Via Ugi reactions to conformationally fixed cyclic peptides
    • Hebach C. Kazmaier. Via Ugi reactions to conformationally fixed cyclic peptides. Chem. Commun. 2003; 596-597.
    • (2003) Chem. Commun. , pp. 596-597
    • Hebach, C.1    Kazmaier, A.2


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